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Annual Report 2011 - Environmental Science & Research

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The Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong><br />

<strong>Annual</strong> <strong>Report</strong> <strong>2011</strong><br />

www.esr.cri.nz


The Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong><br />

Manaaki Tangata Taiao Hoki<br />

Protecting people and their environment through science<br />

Mt Albert<br />

<strong>Science</strong> Centre<br />

Kenepuru<br />

<strong>Science</strong> Centre<br />

NCBID<br />

Wallaceville<br />

Christchurch<br />

<strong>Science</strong> Centre<br />

18 Hampstead Road<br />

Mt Albert<br />

Private Bag 92 021<br />

Auckland 1142<br />

Tel: +64 9 815 3670<br />

Fax: +64 9 849 6046<br />

34 Kenepuru Drive<br />

Porirua<br />

PO Box 50 348<br />

Porirua 5240<br />

Tel: +64 4 914 0700<br />

Fax: +64 4 914 0770<br />

66 Ward Street<br />

Upper Hutt<br />

PO Box 40 158<br />

Upper Hutt 5140<br />

Tel: +64 4 529 0600<br />

Fax: +64 4 529 0601<br />

27 Creyke Road<br />

Ilam<br />

PO Box 29 181<br />

Christchurch 8540<br />

Tel: +64 3 351 6019<br />

Fax: +64 3 351 0010<br />

ISBN 1179 5123


Contents<br />

ESR at a glance 3<br />

Core programme areas 4<br />

Corporate governance 5<br />

Chair and Chief Executive Officer reports 8<br />

Statement of Core Purpose 10<br />

ESR and the Canterbury earthquakes 11<br />

Outcome 1: Safeguard the health of New Zealanders through<br />

improvements in the management of human biosecurity and<br />

threats to public health 13<br />

Outcome 2: Increase effectiveness of forensic science services<br />

applied to safety, security and justice investigations and processes 17<br />

Outcome 3: Enhance protection of New Zealand’s food-based<br />

economy through the management of food safety risks associated<br />

with traded goods 22<br />

Outcome 4: Improve the safety of freshwater and groundwater<br />

resources for human use and the safer use of biowastes 27<br />

Human resources 32<br />

<strong>Research</strong> 33<br />

Information management 34<br />

Capability Fund 35<br />

Financials 37<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 1


2 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


ESR at a glance<br />

The Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong>.<br />

A Crown <strong>Research</strong> Institute (CRI) established in 1992.<br />

<strong>Annual</strong> operating revenue $51.4 million.<br />

9.5% return on equity to shareholders.<br />

Valued public good services provided in New Zealand $44.6 million.<br />

ESR provides science advice and services to government agencies, local<br />

authorities and the private sector.<br />

We are:<br />

> sole provider of forensic services to New Zealand<br />

Police<br />

> Principal science advisor to the Ministry of Health<br />

> Preferred science provider to the New Zealand<br />

Food Safety Authority, New Zealand Customs<br />

Service, Medsafe and the Department<br />

of Corrections<br />

> A science partner of Ministry of Agriculture<br />

and Forestry (MAF)<br />

> <strong>Science</strong> advisor for local authorities, industry<br />

organisations and the private sector.<br />

ESR’s core clients:<br />

> New Zealand Police<br />

> Ministry of Health<br />

> Ministry of Agriculture and Forestry.<br />

<strong>Research</strong> investors:<br />

> Ministry of <strong>Science</strong> and Innovation (MSI)<br />

> Health <strong>Research</strong> Council<br />

> The Royal Society of New Zealand<br />

> Marsden Fund<br />

MSI delegates $5.8m of Capability Funds to ESR<br />

to invest in science and research capability.<br />

Expertise:<br />

> 327 full-time-equivalent (FTE) scientists, technical<br />

specialists and support staff working at four sites:<br />

Auckland, Wellington (Kenepuru and Wallaceville)<br />

and Christchurch.<br />

Our staff cover a range of scientific disciplines and<br />

include public health physicians, environmental<br />

scientists, epidemiologists, chemists, forensic scientists,<br />

toxicologists, molecular biologists, microbiologists,<br />

social scientists, biostatisticians and geoinformaticians.<br />

Core scientific strengths:<br />

> Microbiology and virology (clinical and<br />

environmental)<br />

> Molecular biology<br />

> Chemistry<br />

> Epidemiology<br />

> Risk analysis<br />

> Surveillance<br />

> Social systems<br />

> Toxicology<br />

> <strong>Research</strong>.<br />

Laboratory accreditation:<br />

ESR’s environmental health laboratories and<br />

pharmaceutical and workplace drug testing laboratories<br />

are all accredited to comply with ISO 17025 or ISO<br />

15189 by International Accreditation New Zealand<br />

(IANZ). Some environmental health laboratories are<br />

also World Health Organization (WHO) accredited.<br />

The pharmaceutical laboratories also have Good<br />

Manufacturing Practice (GMP) certification.<br />

All of ESR’s forensic laboratories and operations are<br />

American Society of Crime Laboratory Directors/<br />

Laboratory Accreditation Board International (ASCLD/<br />

LAB) accredited, which also complies with the ISO<br />

17025 standard.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 3


Core programme areas<br />

Forensic<br />

ESR provides the New Zealand justice system with a comprehensive forensic service. This<br />

is underpinned by original research and the latest DNA technology.<br />

> Oversees and manages the New Zealand National DNA Databank.<br />

> Crime scene investigation and evidence recovery.<br />

> Physical evidence investigation.<br />

> DNA profiling, storing and matching.<br />

> Criminal and coronial toxicology.<br />

> Illicit drug analysis, including clandestine laboratory investigation.<br />

> Blood and breath alcohol and drug testing for drivers.<br />

> Pharmaceuticals.<br />

> Workplace drug testing.<br />

> Expert witnesses for court.<br />

> Training.<br />

<strong>Environmental</strong> health<br />

ESR provides key specialised scientific services to the public health sector. It is a core<br />

provider of public health and environmental health scientific services to the Ministry of<br />

Health and MAF.<br />

> Food programme.<br />

> Health programme.<br />

> Water programme.<br />

ESR is a founding partner organisation at the National Centre for Biosecurity and<br />

Infectious Disease NCBID) – Wallaceville.<br />

> Human biosecurity.<br />

> Microbial and chemical forensics.<br />

Social systems<br />

The work of ESR’s social systems group covers three broad areas of interrelated research:<br />

Healthy Communities, Sustainable Development and <strong>Science</strong>, Technology and<br />

Communities.<br />

> Health services improvement.<br />

> Risk and decision making.<br />

> Supporting Canterbury earthquake recovery – stakeholder engagement design<br />

and analysis.<br />

> <strong>Science</strong> for justice outcomes.<br />

4 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Corporate governance<br />

ESR is one of eight CRIs created in 1992 with the reform of New Zealand’s state-funded<br />

science services.<br />

As a CRI, the Institute’s principal activity is to conduct scientific research in accordance with the purpose and<br />

principles of CRIs as set out in sections 4 and 5 of the Crown <strong>Research</strong> Institutes Act 1992. A Statement of Core<br />

Purpose (SCP) further clarifying ESR’s role and responsibilities was published by the Government in late 2010.<br />

ESR is wholly owned by the New Zealand Government and has an independent Board of Directors that is<br />

responsible for its strategic direction and operational performance. ESR has a Board of seven directors including<br />

the Chair.<br />

Responsibility for the operation and administration of the Institute is delegated to the Chief Executive Officer<br />

(CEO), who is accountable to the Board.<br />

The new Ministry of <strong>Science</strong> and Innovation performs the role of protecting the shareholders’ interests and<br />

investment in the Institute. The Statement of Corporate Intent (SCI) and <strong>Annual</strong> <strong>Report</strong> are tabled in parliament.<br />

Board of Directors<br />

Board members from left: Tahu Potiki, Elizabeth Hickey, Patricia Schnauer, Dr Susan Macken (Chair), Dr Judith Johnston,<br />

Ross Peat (Deputy Chair) and Professor Bill Denny.<br />

The Board acts on behalf of, and is accountable to, the Shareholding Ministers (the Minister of Finance and the<br />

Minister of <strong>Science</strong> and Innovation) and fulfils the regulatory expectations laid down in the Companies Act 1993,<br />

the Crown <strong>Research</strong> Institutes Act 1992, the Public Finance Act 1989 and the Crown Entities Act 2004.<br />

Board biographies<br />

Dr Susan Macken – Chair<br />

Dr Susan Macken has BSc and BCom degrees from the University of Auckland, and a PhD in economics from<br />

Cambridge University. She has worked for the World Bank as an economist, held various senior roles at Fletcher<br />

Challenge and is a former Chief Executive of the Problem Gambling Foundation and the Auckland Regional<br />

Economic Development Strategy. She is currently a business consultant and her current directorships include<br />

Bank of New Zealand, New Zealand Treasury, Ultimate Care Group, Fertility Associates and the Auckland<br />

Regional Amenities Funding Board.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 5


Ross Peat – Deputy chair<br />

Ross Peat has a wealth of experience in the IT/software industry. He spent nine years with IBM New Zealand<br />

followed by 14 years at Microsoft New Zealand, the last four as Managing Director. His current directorships<br />

include Healthsoft Limited and several New Zealand IT start-ups.<br />

Professor Bill Denny<br />

Bill Denny is a graduate of the University of Auckland and trained at Auckland and Oxford Universities as<br />

a medicinal chemist. He is currently a co-director of the Auckland Cancer Society <strong>Research</strong> Centre in the<br />

University of Auckland’s School of Medical <strong>Science</strong>s where he has been closely involved in the development of<br />

eight drugs from the Centre into clinical trials, in collaboration with different industrial partners. He is a principal<br />

investigator in the Maurice Wilkins Centre and is co-Chair of the University’s Biopharma <strong>Research</strong> Initiative.<br />

Elizabeth Hickey<br />

Liz Hickey is a company director and chartered accountant. Current directorships include the Southern Cross<br />

Healthcare Group and the New Zealand Institute of Chartered Accountants. She is on the board of the Auckland<br />

Netball Centre, and is a co-opted member of the audit committee of the ASB Community Trust.<br />

Dr Judith Johnston<br />

Dr Judith Johnston has a BA(Hons) from the University of Otago, an MA from the University of Toronto and a<br />

PhD from the University of Auckland. She is Managing Director of her own management consulting company,<br />

Judith Johnston Limited. Judith has many years of experience in the public and private sectors, including with the<br />

Ministry of Justice, Ministry of Health and Department of Health.<br />

Tahu Potiki<br />

Tahu Potiki is Otago based and is affiliated to the iwi of Kai Tahu and Kati Mamoe. He has spent many years<br />

working in Māori development and was the CEO of Te Runanga o Ngāi Tahu for six years. He is now the Otakou<br />

representative to the Te Runanga o Ngāi Tahu tribal council. He has a background working in Māori health and<br />

education and practiced as a qualified social worker for many years.<br />

Tahu has served on four South Island DHBs and is currently on the Southern DHB whilst he is also a serving<br />

board member of the Māori Television Service, New Zealand Council for Educational <strong>Research</strong> and Relationship<br />

Services NZ.<br />

Patricia Schnauer<br />

Patricia Schnauer is a qualified barrister and solicitor and director of Schnauer and Co Limited, a law firm<br />

she established in 1987. In 1996 Patricia became a List Member of Parliament in the first MMP Coalition<br />

Government. She is Deputy Chair of North Shore Hospice and a Trustee of the North Harbour Stadium Trust.<br />

Strategic Leadership Team<br />

The responsibility for the operation and administration of ESR is delegated to the CEO, who heads the Strategic<br />

Leadership Team. This Team develops and implements strategies that keep ESR focused on achieving its goals and<br />

strategic business objectives.<br />

In May <strong>2011</strong> the Chief Executive, Dr John Hay, resigned and acting CEO, Dr Fiona Thomson-Carter, was<br />

appointed for the remainder of the financial year.<br />

CEO (acting)<br />

GM <strong>Environmental</strong> Health (acting)<br />

GM Forensic<br />

GM Business Development and Marketing<br />

GM Finance<br />

Chief Information Officer<br />

GM Human Resources<br />

GM <strong>Science</strong> and RESEARCH<br />

Dr Fiona Thomson-Carter<br />

Dr Virginia Hope<br />

Dr Keith Bedford<br />

David Talbot<br />

Peter O’Shea<br />

Leo Morta<br />

Terry McCaul<br />

Dr Val Orchard<br />

6 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 7


Chair’s report<br />

2010-<strong>2011</strong> was a momentous year for New Zealand. For ESR, as for many<br />

organisations, the Christchurch earthquakes presented significant challenges<br />

to our people and our operations, and the slower and more protracted<br />

recovery in the economy impacted growth.<br />

After five years of year on year increases in earnings, ESR’s revenue has entered a<br />

consolidation phase with growth from existing business streams projected to be slow in the<br />

medium term. The organisation is focussed on revenue diversification through strategic<br />

initiatives that include acquisitions, new clients, and international sales. We expect to<br />

grow these new revenue sources significantly over the next three years.<br />

Our financial results for 2010-<strong>2011</strong> reflect the impact of Christchurch events and<br />

continued fiscal restraint of government clients. Revenue at $51.4M was $2.0M down on<br />

budget. The Forensic business was ahead of budget in revenue and contribution, while<br />

both the <strong>Environmental</strong> Health and Social Systems businesses were significantly behind in<br />

both revenue and contribution. <strong>Research</strong> revenue was down on last year, and on budget,<br />

due to a reduction in ESR’s government research funding and limited new research<br />

funding. The net deficit in operational business contribution was substantially offset by<br />

savings in infrastructure costs.<br />

Despite these challenges ESR achieved over 8% return on equity on operational<br />

performance (9.5% after non-recurring taxation adjustments), and a pleasing net profit of<br />

$3.2M after tax, which was ahead of budget.<br />

ESR’s environment was positively impacted by the implementation of the<br />

recommendations of the Crown <strong>Research</strong> Institute Taskforce. The board completed a new<br />

Statement of Core Purpose. Developed in consultation with our clients and government,<br />

it provides a clear set of national outcomes in the justice, health and environmental<br />

sectors. Key areas of responsibility involve providing science and research services related<br />

to human biosecurity, public health, food and water safety, and forensic science.<br />

May <strong>2011</strong> marked the end of a rewarding relationship with the organisation for our Chief<br />

Executive Officer, Dr John Hay. John’s significant contribution, both as a scientist and<br />

leader, meant that he left ESR as a strong robust company. The board recruited a new<br />

CEO, Graham Smith, who takes up his position in August <strong>2011</strong>. In the interim, ESR’s<br />

General Manager <strong>Environmental</strong> Health, Dr Fiona Thomson-Carter, is Acting Chief<br />

Executive.<br />

We look forward to the new financial year and the opportunities for ESR to deliver<br />

on its Statement of Core Purpose through the continued provision of its science and<br />

research, and the transfer of technology and knowledge with key stakeholders, including<br />

government, industry, the community and Māori.<br />

My thanks go to the management and staff of ESR for their professionalism and<br />

commitment in a challenging year. ESR’s continual delivery of outstanding operational<br />

and research science to New Zealand’s health and justice sectors is a tribute to them all.<br />

I also acknowledge the work and support of my board colleagues in undertaking the<br />

governance of ESR.<br />

Dr Susan Macken<br />

Chair<br />

8 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Acting CEO’s report<br />

This was no ordinary year for any organisation in New Zealand. Reflecting in<br />

particular on the challenges posed to our Christchurch-based staff and their<br />

science during this extraordinary financial year, it is remarkable that we have<br />

been able to largely continue to deliver critical science to our core clients,<br />

despite the major earthquakes and subsequent aftershocks in Canterbury.<br />

It is testament to the professionalism and resilience of our Christchurch staff that forensic<br />

and environmental health services provided from our Christchurch <strong>Science</strong> Centre,<br />

although disrupted at times, continued. ESR scientists played key roles in the earthquake<br />

response and recovery processes most notably in Disaster Victim Identification, informing<br />

public health actions as a result of surveys of the Christchurch population, and analysis<br />

and advice of health hazards posed by liquefaction silts and contaminated water supplies.<br />

Our scientists made these significant contributions to their community while dealing with<br />

the day-to-day earthquake-related difficulties encountered in their personal lives. ESR has<br />

been proud to be able to support our staff in every way possible.<br />

In the more localised CRI environment, the first real changes invoked by implementation<br />

of the CRI Taskforce recommendations were apparent with the development of the new<br />

Statement of Core Purpose and Statement of Corporate Intent. ESR’s Core Purpose is to<br />

deliver benefit to New Zealand’s Justice and Health sectors.<br />

Continuing constraints on public sector funding affected ESR operations and we have<br />

adapted to, and planned for, the new environment while progressing our strategic<br />

initiatives and seeking to diversify and grow new revenue streams. To aid these endeavours,<br />

ESR has effected change internally, notably in planning the replacement of our Laboratory<br />

Information Management System, targeted management training and taking actions based<br />

on the findings of a staff culture survey. These initiatives will stand us in good stead to face<br />

the challenges to come.<br />

A particular highlight was the refurbishment of our Health Programme laboratories at<br />

the Kenepuru <strong>Science</strong> Centre, officially opened by the Minister of Health, the Hon Tony<br />

Ryall, in June.<br />

A customer satisfaction survey conducted during the year demonstrated that ESR’s services<br />

are much appreciated by our clients with 89% of those surveyed expressing significant<br />

levels of satisfaction. This outstanding result underscores the professionalism our staff<br />

brings to every aspect of their working lives at ESR.<br />

ESR’s science and expertise was featured in several national media events during the<br />

year including our work related synthetic cannabinoids, the introduction of spherical<br />

photography to explain forensic evidence in court, and the outbreak of E. coli O104 in<br />

Europe.<br />

Many varied collaborations and interactions with our international scientific networks<br />

ensured our science is continually refreshed and achieves the standards of international<br />

best practice. ESR’s new <strong>Science</strong> Advisory Panel is comprised of three international experts<br />

in their fields; we look forward to having their input into our science programmes.<br />

When meeting new ESR staff, I usually take the opportunity to say that no two days at<br />

ESR are ever the same; that assertion can also be made for the financial year just ended.<br />

An extraordinary year for ESR and New Zealand.<br />

Dr Fiona Thomson-Carter<br />

Chief Executive Officer – acting<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 9


Statement of Core Purpose<br />

A key recommendation of the CRI Taskforce was for the Government<br />

to publish a SCP for each CRI, defining its purpose, the outcomes to<br />

be achieved, the scope of operation and the operating principles. ESR<br />

worked with clients, stakeholders and MSI over several months to<br />

develop its SCP, which was released in November 2010.<br />

ESR’s purpose is to deliver enhanced scientific and research services to the public health,<br />

food safety, security and justice systems and the environmental sector to improve the<br />

safety and contribute to the economic, environmental and social wellbeing of people and<br />

communities in New Zealand.<br />

SCP Outcomes<br />

ESR will fulfil its purpose through the provision of research and scientific services and<br />

the transfer of technology and knowledge in partnership with key stakeholders, including<br />

government, industry, the community and Māori, to:<br />

Outcome 1: Safeguard the health of New Zealanders through improvements in the<br />

management of human biosecurity and threats to public health<br />

Outcome 2: Increase the effectiveness of forensic science services applied to safety,<br />

security and justice investigations and processes<br />

Outcome 3: Enhance the protection of New Zealand’s food-based economy through the<br />

management of food safety risks associated with traded goods<br />

Outcome 4: Improve the safety of freshwater and groundwater resources for human use<br />

and the safer use of biowastes.<br />

The full SCP is available on www.esr.cri.nz.<br />

Strategic initiatives<br />

Consistent with our SCP, revenue diversification initiatives were set in four areas:<br />

> Enhancing and expanding our government service business by investing in and<br />

acquiring new scientific capabilities, technologies and enterprises<br />

> Expanding our international scientific and consultancy services and research<br />

collaborations to access new technologies and research revenue<br />

> Making use of online and digital technologies to deliver smart, new, effective, efficient<br />

and essential services to clients in New Zealand and overseas<br />

> Engaging with industry. Working with sector partners and commercialisation entities,<br />

ESR will utilise and transfer its intellectual property, intellectual knowledge and<br />

professional expertise to benefit New Zealand.<br />

10 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


ESR and the Canterbury earthquakes<br />

Our staff<br />

Immediately following the Christchurch earthquake on 22 February <strong>2011</strong>, the ESR<br />

emergency response team convened with an incident controller in Wellington. Contact<br />

with our Christchurch <strong>Science</strong> Centre (CSC) ensured that all staff had been evacuated<br />

and the site was closed until a full structural assessment could be made. Regular<br />

communication was maintained with Christchurch staff until the site re-opened for<br />

business.<br />

> We are proud of our staff who re-established our Christchurch-based business quickly<br />

and who continue to produce high-calibre science under difficult circumstances.<br />

> Staff support mechanisms were put in place, including emergency accommodation,<br />

special leave, and travel for staff and families so they could have a break with friends<br />

and relatives.<br />

Sharing our quake-safe building<br />

As soon as the CSC building was declared safe and structurally sound, we offered business<br />

accommodation to affected CRIs and other local and central government agencies. The<br />

National Radiation Laboratory’s Japanese earthquake response team based themselves at<br />

the CSC as their own building was in a ‘red zone’. The University of Canterbury also used<br />

our meeting rooms for lectures.<br />

Operational support response<br />

> ESR forensic staff assisted with disaster victim identification (DVI). Specialist DNA<br />

staff were dispatched to Christchurch immediately and worked with a number of other<br />

agencies for several weeks under the direction of the coroner and police at Burnham<br />

Military Camp. The DNA laboratory in Auckland analysed samples.<br />

> ESR staff assisted Environment Canterbury and the Christchurch City Council to<br />

investigate post-quake water quality in the Avon River by assessing contaminant risks<br />

using our specialist faecal tracking tools.<br />

> We provided advice to Christchurch Community and Public Health on the security of<br />

groundwater sources in the Canterbury region concerning well-head protection around<br />

bores and aquifer movements.<br />

> Following the September, February and June Canterbury earthquakes, ESR provided<br />

information to health authorities and councils on the public health risks posed by<br />

exposure to liquefaction silt and dust.<br />

> The Health Intelligence team co-ordinated a phone survey assessing the health needs of<br />

Christchurch residents following the February quake. The Christchurch District Health<br />

Board used the survey to address problems of access to essential health services, such as<br />

GPs, pharmacies and safe drinking water.<br />

> ESR reported weekly to the Ministry of Health on Christchurch residents’ health<br />

status to give early warnings of local outbreaks of gastroenteritis and influenza. This<br />

information was complemented by ESR’s general surveillance and laboratory reference<br />

data, which tracks diseases and outbreaks nationwide.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 11


12 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


statement of core purpose Outcome 1<br />

Safeguard the health of New Zealanders<br />

through improvements in the management of<br />

human biosecurity and threats to public health<br />

As principal science advisor, ESR provides the Ministry of Health and the<br />

health sector with robust information for public health action and evidencebased<br />

policy-making.<br />

At the National Centre for Biosecurity and Infectious Disease (NCBID) we continued<br />

to work closely with the Ministry of Agriculture and Forestry (MAF) on operational and<br />

research projects.<br />

We provide health science services to district health boards and local government and offer<br />

national reference laboratory testing for hospital, community and medical laboratories.<br />

We are also responsible for collecting, overseeing and managing and distributing<br />

important health intelligence data and collections. We also undertake microbiological and<br />

epidemiological investigations into infectious disease outbreaks.<br />

With these comprehensive laboratory and disease surveillance data and systems, we<br />

provide advice and information to the health sector on a real-time basis. This includes<br />

issuing alerts to public health services of any unusual or increased disease activity locally<br />

and nationally.<br />

This year we:<br />

> issued 43 alerts to public health units based on our early warning notifiable disease<br />

surveillance<br />

> managed EpiSurv, New Zealand’s notifiable disease surveillance system<br />

> issued weekly, monthly, quarterly and annual surveillance and other reports<br />

> operated surveillance and health information websites, including www.surv.esr.cri.nz<br />

> managed the National Culture Collection – medical section<br />

> provided an outbreak investigation course for all public health units<br />

> presented at the 2010 Health Protection Officer training workshop<br />

> participated in multi-agency disease outbreak exercises.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 13


Refurbishment of reference and other disease<br />

laboratories<br />

ESR spent over $1 million upgrading laboratories at the Kenepuru <strong>Science</strong> Centre. The<br />

work was completed in January <strong>2011</strong> and ensured that facilities were up to date and<br />

continued to meet all user and accreditation requirements. The laboratories were officially<br />

opened by the Minister of Health, Hon Tony Ryall in June <strong>2011</strong>.<br />

Clinical advisory panel established<br />

An external advisory panel of New Zealand and Australian microbiology experts was<br />

established to provide us with advice on laboratory testing and microbiology issues,<br />

including outbreak responses and infectious disease emergencies and the implementation<br />

and monitoring of performance and quality improvement standards.<br />

Food pathogens – lab survey<br />

An ESR survey of all New Zealand laboratories investigated how testing for the main food<br />

safety pathogens was undertaken. We also looked at the processes used by public health<br />

services for case investigation into food-related illnesses. This information will assist MAF<br />

(Food Safety) to identify priority actions related to testing and investigation.<br />

Vaccine store<br />

ESR manages the purchase, storage and distribution of vaccines for the national<br />

immunisation programme. This year we managed stockpiles of the MMR vaccine<br />

purchased for a measles outbreak.<br />

> We developed and ran the tender for the National Immunisation Schedule for <strong>2011</strong>-<br />

2014 and performed an evaluation for the Ministry of Health. This led to the selection<br />

of a new pneumococcal vaccine and a significant reduction in the Ministry of Health’s<br />

annual budget for vaccine purchases.<br />

14 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Focus on antibiotic resistance<br />

The Antibiotic Reference Laboratory received increasing numbers of bacterial isolates to<br />

investigate for emerging mechanisms of resistance. New resistance genes were identified<br />

for the first time in New Zealand, including the New Delhi strain, which is resistant to<br />

many antibiotics. All four patients identified here had received healthcare in India. Two<br />

other antibiotic-resistant strains were also identified here for the first time: KPC and<br />

OXA-48.<br />

Hospital-acquired infections<br />

ESR provides specialist typing for hospital laboratories investigating incidences of<br />

hospital-acquired infections. Increased funding this year enabled us to increase the rate<br />

of sample processing and implement new methods to provide faster and internationally<br />

comparable data.<br />

The incidence of hospital-acquired Clostridium difficile around the world has risen<br />

significantly and the emergence of hypervirulent strains has increased the need to monitor<br />

this bacterium.<br />

> We introduced specialist testing to identify these strains.<br />

> To date, hypervirulent strains have been identified from three patients in New Zealand<br />

hospitals.<br />

Survey of antimicrobial-resistant foodborne bacteria<br />

A survey undertaken for MAF indicated no human health implications from antimicrobial<br />

resistance in New Zealand food-producing animals and fresh produce.<br />

In a 12-month period from October 2009, ESR assessed antimicrobial resistance among<br />

Campylobacter, Salmonella, Escherichia coli and Enterococci isolated from carcasses of calves,<br />

pigs and broiler poultry in New Zealand abattoirs and processing plants. The assessment<br />

provided baseline information to monitor changes in resistance among bacteria from foodproducing<br />

animals, and information to guide policy decisions on the use of antimicrobials<br />

in animal husbandry.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 15


<strong>Research</strong> case study –<br />

international collaboration<br />

on flu<br />

NCBID partners ESR and MAF,<br />

and the World Health Organization<br />

Collaborating Centre in the United<br />

States, are investigating influenza<br />

virus circulation and exposure in New<br />

Zealand pigs. <strong>Research</strong> begun this year is<br />

providing important information on the<br />

ecology of virus circulation in pigs, the<br />

potential for inter-species transmission<br />

and the implications for animal and<br />

human health.<br />

Pigs have receptors for both human<br />

and avian viruses and can act as mixing<br />

vessels for the creation of new viruses.<br />

The recent pandemic influenza virus<br />

genetically originated from swine<br />

influenza viruses, but how it entered<br />

the human population is still not really<br />

understood.<br />

Earlier MAF surveys established that<br />

most New Zealand pigs had been<br />

infected with influenza AH3 viruses at<br />

some time in their lives. A further joint<br />

study undertaken this year by ESR,<br />

MAF and WHO showed an overall<br />

prevalence of 3.6% Influenza A antibody<br />

from porcine serum samples.<br />

These findings led to this new research<br />

project. Respiratory and blood samples<br />

will be taken from abattoir pigs to<br />

identify current circulating influenza<br />

strains and patterns of exposure. This<br />

information will be compared with our<br />

surveillance information on human<br />

influenza viruses.<br />

National Influenza Centre<br />

ESR is responsible for New Zealand’s national influenza surveillance. We are the contact<br />

nationally and internationally for the virological and epidemiological surveillance of<br />

influenza and recommend the composition of the annual influenza vaccine.<br />

> This year all the various streams of surveillance monitoring of flu were consolidated at<br />

ESR. In addition to our GP sentinel and laboratory-based surveillance, we took over<br />

reporting using Healthline and HealthStats data.<br />

> Flu information is analysed, reported and distributed weekly, monthly and annually<br />

to relevant national and international organisations. Data is analysed for any change,<br />

providing an early warning system of any real or potential outbreaks of influenza.<br />

> We continued our comprehensive testing, surveillance and research associated with the<br />

influenza pandemic.<br />

> ESR assessed the New Zealand experience with the second complete wave of pandemic<br />

influenza A(H1N1)09 in 2010. Hospitalisation and other rates suggested the overall<br />

impact in 2010 was about half to two-thirds that of the first wave in 2009.<br />

<strong>Research</strong> collaborations lead to new services<br />

New ways of detecting new microbes were established. Associate Professor Thomas Briese<br />

from Columbia University, an internationally recognised ‘microbe hunter’ and a <strong>2011</strong><br />

ESR International Fellow, spent time this year at ESR’s NCBID providing guidance<br />

and advice to staff. This microbe detection work is being funded through our Capability<br />

Funding.<br />

> Detection methods were originally developed at New York’s Columbia University and<br />

have been used to identify new viruses, including the third species of the common<br />

cold. New viruses or microbes can emerge from animals and cross into humans, or<br />

cause unusual illnesses in humans that have not previously been recognised.<br />

> A Health <strong>Research</strong> Council-funded study is using new technologies to find out what<br />

bacteria and viruses are causing stomach illnesses in New Zealanders. Most people<br />

don’t visit their doctors for stomach upsets or diarrhoea, and of those who do go, only<br />

20% are ever diagnosed by routine testing.<br />

Medicine testing<br />

We continued to monitor medicines for Medsafe, giving particular attention to ‘herbal<br />

medicine’ products, which are sometimes found to contain undeclared prescription<br />

medicines. Several varieties of ‘herbal’ erectile dysfunction product were withdrawn from<br />

sale this year following the identification of undeclared medicines in product casing.<br />

Supporting New Zealand Defence Forces overseas<br />

The New Zealand Defence Force (NZDF) operates its own Medical Stores and repacks<br />

pharmaceutical products into packs suitable for use in the field. The repacking operation<br />

is licensed by Medsafe and operates under the requirements of Good Manufacturing<br />

Practice. Determining the stability of pharmaceutical products and their expiry dates<br />

in these repackaged systems is critical to ensuring they are suitable for use by defence<br />

personnel, especially in combat situations.<br />

Drug and alcohol services<br />

Our social scientists undertook a comprehensive review for the Ministry of Health of<br />

how opioid substitution treatment is delivered in New Zealand. This work included<br />

interviewing stakeholders and identifying opportunities for improvement to the system.<br />

> It was funded by the Australian Drugs Policy Modelling Programme to provide a<br />

New Zealand comparison with Australian studies into similar services.<br />

16 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


statement of core purpose Outcome 2<br />

Increase effectiveness of forensic science<br />

services applied to safety, security and justice<br />

investigations and processes<br />

ESR delivers cost-effective forensic services from the crime scene to the courtroom,<br />

providing independent science underpinning an effective and trusted criminal justice<br />

system. We directly support Government-agreed justice sector outcomes through the<br />

provision of mutually agreed contracted services for key government agencies.<br />

We support:<br />

> New Zealand Police in meeting its forensic priorities, key initiatives in its SCI, and<br />

a significant number of its cross-sector outcomes<br />

> the Department of Corrections in reducing drug use among prison inmates<br />

> courts through the provision of timely, high-quality scientific evidence supporting<br />

the criminal justice process<br />

> coroners and pathologists through toxicological and other investigations for<br />

coronial inquiries<br />

> New Zealand Customs Service border-control activities, particularly those related<br />

to drug seizures and supply<br />

> road safety agencies through drink- and drugged-driver testing.<br />

Forensic work also supports other government agencies through the provision<br />

of scientific knowledge, monitoring and advice on legal highs, party pills and<br />

prescription medicines to Medsafe and the Ministry of Health.<br />

Every day ESR’s 140 forensic staff investigate crime scenes, analyse a<br />

range of evidence in the laboratory, obtain and process DNA profiles,<br />

provide intelligence to investigators and present courtroom evidence<br />

as independent expert witnesses.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 17


Case study: DNA Databank<br />

turnaround times<br />

ESR worked with New Zealand Police<br />

to reduce turnaround times in ‘volume<br />

crime’ DNA evidence from an average<br />

of 28 days to five days or fewer (volume<br />

crime is defined as burglaries and thefts<br />

from vehicles). Under the terms of our<br />

Service Level Agreement with New<br />

Zealand Police these results are now<br />

provided within five days of police<br />

submitting samples. This turnaround<br />

time compares with a one-month<br />

average in Australia and up to two years<br />

in some USA states.<br />

In addition this year:<br />

> turnaround times for serious crime<br />

DNA analysis improved<br />

> profiles from individuals were<br />

generated and loaded to the National<br />

DNA Databank within three or four<br />

days of ESR receiving the samples<br />

> the link rate continued to be one<br />

of the best of any criminal DNA<br />

database in the world – around two<br />

out of every three profiles loaded<br />

provided investigators with links<br />

between an individual and a crime<br />

or crimes.<br />

At the end of June <strong>2011</strong>, more than<br />

123,000 individual profiles and<br />

25,000 crime samples were held in the<br />

databases that make up the National<br />

DNA Databank.<br />

Disaster victim identification<br />

One of our major contributions during the year was to the DVI operations following the<br />

earthquake in Christchurch on 22 February <strong>2011</strong>. DNA scientists joined the police and<br />

coronial DVI team at Burnham immediately after the quake, working round the clock for<br />

several weeks assisting with identifications. We undertook DNA sample analysis at our<br />

specialist DNA laboratory.<br />

DNA<br />

New Zealand’s forensic service provider model is cost effective and efficient: New Zealand<br />

is one of the few countries that doesn’t have a DNA backlog, and our turnaround times<br />

in DNA analysis are among the best in the world. As custodian of the National DNA<br />

Databank, ESR ensures that it is used as a primary criminal intelligence tool, is managed<br />

efficiently and meets all legislative standards.<br />

> Through the development of mutually agreed end-to-end processes with justice sector<br />

partners, this year we again improved the delivery of forensic services to investigators<br />

and the courts.<br />

> As a result of world-leading ESR research, a new DNA analysis technique was<br />

introduced for use in criminal investigations. It enables the identification of body<br />

fluid, which can be important in determining the source of a DNA profile, or in<br />

corroborating different versions of events.<br />

Crime scene investigations<br />

We continued to provide a 24/7 scene-callout service from our forensic service centres<br />

located in Christchurch, Wellington and Auckland, and from our physical evidence<br />

laboratory, which specialises in firearm-related incidents.<br />

> 238 serious crime scenes were attended.<br />

18 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Forensic toxicology<br />

ESR provides New Zealand’s only forensic toxicology service, supporting the work of<br />

coroners, pathologists, New Zealand Police and Child, Youth and Family. Toxicological<br />

investigations determine the presence of alcohol, drugs, solvents, inhalants and poisons in<br />

samples.<br />

> We invested in a major piece of analytical equipment that allows a more rapid<br />

and specific identification of drugs, poisons and toxins for coronial and criminal<br />

toxicological investigations.<br />

> We tested, analysed and reported on 3837 samples for 1353 coronial cases and 122<br />

toxicological samples for serious crime cases.<br />

Drink- and drugged-driver testing<br />

ESR undertakes analysis for all evidential blood alcohol samples taken from drivers under<br />

the Land Transport Act 1998 and drugged-driver testing under provisions in the Land<br />

Transport Amendment Act 2009.<br />

> More than 6600 blood samples for alcohol and 139 drugged-driver samples were<br />

analysed.<br />

> 205 breath-alcohol-testing devices were calibrated, with our analysts available to<br />

present evidence in court.<br />

Forensic research<br />

ESR invests in forensic research through the Capability Fund to improve operational<br />

casework delivery. This year a new world-leading RNA analysis technique was transferred<br />

from research to operational use.<br />

> We collaborated with the University of Auckland on our joint postgraduate forensic<br />

science programme and hosted 21 national and international forensic science students.<br />

> <strong>Research</strong> and training programmes on blood spatter analysis were provided to USA<br />

forensic agencies.<br />

Case study: Crime scene virtual<br />

tour successfully used in court<br />

Jurors in a homicide trial took a<br />

virtual walk through the crime scene<br />

in a presentation used to explain the<br />

extensive forensic evidence associated<br />

with the case. The technology reduced<br />

court time spent explaining complex<br />

evidence and could alleviate the need<br />

for jurors to travel to the crime scene,<br />

therefore saving the justice system<br />

time and cost. It was the result of a<br />

research project evaluating the use of<br />

photographic and laser scanning in<br />

recording evidence at crime scenes.<br />

The technology was trialled in several<br />

other homicide investigations and is<br />

likely to be utilised to deliver detailed<br />

forensic evidence in several further court<br />

cases in the coming year.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 19


Links and knowledge transfer with<br />

justice sector<br />

ESR’s scientific services are provided to a range of justice sector players. We hold regular<br />

meetings with Crown solicitors and other judicial representatives. We provide lectures,<br />

presentations and training to the wider justice sector, including the Criminal Bar<br />

Association, Crown solicitors and the judiciary. We transfer forensic knowledge through<br />

training programmes to New Zealand Police and the New Zealand Customs Service.<br />

> New Zealand Police gave ESR a 91% overall satisfaction rating in a client survey.<br />

> ESR forensic staff were involved in and presented at the following Royal New Zealand<br />

Police College courses:<br />

– Three adult sexual assault courses<br />

– Five detective induction courses<br />

– A luminol photography course<br />

– A fire investigation – forensic awareness training course<br />

– The Scene of Crime Officer crime scene foundation course<br />

– The Scene of Crime Officer advanced course.<br />

20 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 21<br />

Focus on drugs<br />

ESR provides a range of scientific services related to drugs to New Zealand<br />

Police, the New Zealand Customs Service, the Department of Corrections’<br />

prison service, the Ministry of Health, Medsafe and the coroners. This year we<br />

also became the sole commercial provider of drug testing in hair for Australia.<br />

Our drug services include:<br />

> prisoner drug testing for the Department of Corrections<br />

> analysing substances seized at the border for the New Zealand Customs Service and<br />

providing advice to support border agency operations<br />

> testing party pills, herbal medicines and other drugs for Medsafe and the Ministry of<br />

Health<br />

> analysing and advising on drug trends for government agencies<br />

> drugged-driver testing for New Zealand Police and the courts<br />

> methamphetamine laboratory investigations, decommissioning illegal meth labs, and<br />

analysing methamphetamine-associated drugs for border control and New Zealand<br />

Police<br />

> hair testing of P lab kids: Hair testing of children exposed to P lab operations found<br />

they had similar drug levels to those in adult users. This test enables police to link<br />

children to methamphetamine labs more accurately, and can be used as evidence in<br />

child neglect cases.<br />

Testing Kronic and other synthetic cannabinoids<br />

ESR tests revealed that two popular brands of legal synthetic cannabinoids contained<br />

illegal prescription medicine. These results led to an immediate Ministry of Healthordered<br />

recall of the products. A further 40 products available for sale in New Zealand<br />

were tested to establish exactly what was in them and if they contained any illegal<br />

substances. ESR identified a number of synthetic cannabinoids with ten of the products<br />

having four or more present.<br />

> ESR has included testing for synthetic cannabinoids in its workplace drug testing<br />

programme since July <strong>2011</strong><br />

> The first ‘Temporary Class Drug Notice’ under a new amendment to the Misuse of<br />

Drugs Act, was introduced by Government to deal with the situation.<br />

Keeping an eye on ‘Ecstasy’<br />

Illicit drugs laboratory staff have been monitoring the substances found in ‘Ecstasy’<br />

tablets. The ready market for legal party drugs has seen a significant number of novel<br />

drugs and substances appear in Ecstasy tablets, some of which infringe the ‘controlled<br />

drug analogue’ provisions of the New Zealand Misuse of Drugs Act 1975, and are illegal.<br />

> We found five illegal drug types in Ecstasy circulating in New Zealand, as well as some<br />

legal substances.<br />

Workplace drug testing<br />

ESR continued to provide alcohol- and drug-testing services to more than 1500<br />

New Zealand companies and undertook prisoner drug testing for the Department of<br />

Corrections.<br />

> We introduced a new hair test for long-term alcohol abuse.<br />

> Improved efficiencies in drugs-in-hair testing delivered faster reporting times and<br />

reduced costs for service users.<br />

> Investment in new analytical equipment enabled us to offer clients a full commercial<br />

oral fluid drug testing service.<br />

Border control – training Customs officers<br />

We delivered drug and forensic awareness training to more than 100 Customs officers<br />

in Auckland, Wellington and Christchurch. The training was designed to help Customs<br />

officers deal safely with illicit drugs and precursors, identify forensic evidence and support<br />

investigations right through to court prosecutions.<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Comparison of ESR’s<br />

Urine, Oral fluid and Hair<br />

drug testing services<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk<br />

on (04) 914 0731<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

www.esr.cri.nz<br />

Ur<br />

drug tes<br />

wor<br />

What does a positive result mean?<br />

A positive result means that the person tested has consumed<br />

drugs recently and has drugs or their metabolites in their<br />

system to a measured level. The measured level is above the<br />

cut-off levels determined by the AS/NZS 4308: 2008 urine<br />

testing standard.<br />

Drug detection times in urine.<br />

The detection times differ for individual drugs but essentially<br />

drugs can be detected in urine from 4 hours and up to 20 days<br />

following use.<br />

Is urine testing the best testing option<br />

for my business?<br />

Urine testing for drugs has been widely used in New Zealand<br />

workplaces for many years. ESR laboratory urine testing is<br />

proven to be a robust and effective testing method when used<br />

in conjunction with a company’s drug testing policy.<br />

Oral Fluid and Hair testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2 08 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with screening by i munoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with scr ening by i munoassay and<br />

confirmation of any positive scr en results by mass<br />

spectrometry before reporting<br />

Laboratory based with analysis by ma spectrometry<br />

Confirmation only testing available for urine specimens<br />

scr ened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite scr ening is not reliable for ca nabinoids<br />

Cut-o f<br />

Levels/ Target<br />

Concentrations<br />

Cut-o f levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-o f levels or target concentrations documented<br />

Cut-o f levels reflect recent, relatively recent o regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for cannabis “Hours” for cannabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up t one year<br />

Can be up to thr e w eks after chronic use (i.e: more<br />

than 5 ca nabis cigare tes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

ca nabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is possible but laboratories<br />

and co lectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witne sed co lection<br />

Adulteration is not po sible<br />

Robust collection procedures by NZQA certified co lectors<br />

greatly reduce the risk of this o cu ring<br />

Substitution is most unlikely due to co lection by a trained<br />

co lector and chain of custody requirements<br />

Cannabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of cannabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not bl od levels<br />

Tests for THC and metabolites<br />

Pa sive Inhalation<br />

of Cannabis<br />

Testing wi l not give a positive result a the cut-o f levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no possibility<br />

of measuring pa sive inhalation<br />

Advantages Used extensively A positive result indicates use within a short time prior to<br />

co lection. This gives a stronger indication tha the person<br />

was “at risk” a the time of co lection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal challenge Some drug levels (not ca nabis) can be related to<br />

bl od levels<br />

Non invasive co lection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was a the time of co lection<br />

Witne sed co lection<br />

A plication Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

G od for post-incident and post rehabilitation Suitable for use in medico-legal, family and crimina law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contac the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Alcohol<br />

in the workplace<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk on (04) 914 0731<br />

FAQs<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

Replace<br />

image<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2008 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with analysis by mass spectrometry<br />

Confirmation only testing available for urine specimens<br />

screened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

oth the parent drug and/or their metabolites Onsite screening is not reliable for cannabinoids<br />

umented No cut-off levels or target concentrations documented<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug in<br />

hair. It is likely that the exposure would have to be at a high<br />

level and for a prolonged period for the drug to be detected<br />

in the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Alcohol<br />

in the workplace<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk on (04) 914 0731<br />

FAQs<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Comparis<br />

Urine, Oral<br />

drug test<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Urine<br />

drug testing in the<br />

workplace<br />

What does a positive result mean?<br />

A positive result means that the person tested has consumed<br />

drugs recently and has drugs or their metabolites in their<br />

system to a measured level. The measured level is above the<br />

cut-off levels determined by the AS/NZS 4308: 2008 urine<br />

testing standard.<br />

Drug detection times in urine.<br />

The detection times differ for individual drugs but essentially<br />

drugs can be detected in urine from 4 hours and up to 20 days<br />

following use.<br />

Is urine testing the best testing option<br />

for my business?<br />

Urine testing for drugs has been widely used in New Zealand<br />

workplaces for many years. ESR laboratory urine testing is<br />

proven to be a robust and effective testing method when used<br />

in conjunction with a company’s drug testing policy.<br />

Oral Fluid and Hair testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Replace<br />

image<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Comparison of ESR’s<br />

Urine, Oral fluid and Hair<br />

drug testing services<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk<br />

on (04) 914 0731<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

www.esr.cri.nz<br />

Ur<br />

drug tes<br />

wor<br />

What does a positive result mean?<br />

A positive result means that the person tested has consumed<br />

drugs recently and has drugs or their metabolites in their<br />

system to a measured level. The measured level is above the<br />

cut-off levels determined by the AS/NZS 4308: 2008 urine<br />

testing standard.<br />

Drug detection times in urine.<br />

The detection times differ for individual drugs but essentially<br />

drugs can be detected in urine from 4 hours and up to 20 days<br />

following use.<br />

Is urine testing the best testing option<br />

for my business?<br />

Urine testing for drugs has been widely used in New Zealand<br />

workplaces for many years. ESR laboratory urine testing is<br />

proven to be a robust and effective testing method when used<br />

in conjunction with a company’s drug testing policy.<br />

Oral Fluid and Hair testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2008 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with scr ening by immunoa say and<br />

confirmation of any positive scr en results by ma s<br />

spectrometry before reporting<br />

Laboratory based with scr ening by i munoa say and<br />

confirmation of any positive scr en results by ma s<br />

spectrometry before reporting<br />

Laboratory based with analysis by mass spectrometry<br />

Confirmation only testing available for urine specimens<br />

screened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite scr ening is not reliable for ca nabinoids<br />

Cut-o f<br />

Levels/ Target<br />

Concentrations<br />

Cut-o f levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-off levels or target concentrations documented<br />

Cut-off levels reflect recent, relatively recent o regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for cannabis “Hours” for ca nabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up t one year<br />

Can be up to thr e w eks after chronic use (i.e: more<br />

than 5 cannabis cigare tes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

ca nabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is possible but laboratories<br />

and collectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witne sed co lection<br />

Adulteration is not po sible<br />

Robust collection procedures by NZQA certified collectors<br />

greatly reduce the risk of this occurring<br />

Substitution is most unlikely due to co lection by a trained<br />

collector and chain of custody requirements<br />

Ca nabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of ca nabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not blood levels<br />

Tests for THC and metabolites<br />

Passive Inhalation<br />

of Cannabis<br />

Testing will not give a positive result at the cut-o f levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no po sibility<br />

of measuring pa sive inhalation<br />

Advantages Used extensively A positive result indicates use within a shor time prior to<br />

co lection. This gives a stronger indication tha the person<br />

was “at risk” a the time of co lection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal cha lenge Some drug levels (not ca nabis) can be related to<br />

bl od levels<br />

Non invasive collection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was at the time of collection<br />

Witne sed co lection<br />

A plication Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

G od for post-incident and post rehabilitation Suitable for use in medico-legal, family and criminal law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contac the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Alcohol<br />

in the workplace<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk on (04) 914 0731<br />

FAQs<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

Replace<br />

image<br />

FAQ<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the previous<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2008 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with analysis by mass spectrometry<br />

Confirmation only testing available for urine specimens<br />

screened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite screening is not reliable for cannabinoids<br />

Cut-off<br />

Levels/ Target<br />

Concentrations<br />

Cut-off levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-off levels or target concentrations documented<br />

Cut-off levels reflect recent, relatively recent or regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for cannabis “Hours” for cannabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up to one year<br />

Can be up to three weeks after chronic use (i.e: more<br />

than 5 cannabis cigarettes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

cannabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is possible but laboratories<br />

and co lectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witnessed collection<br />

Adulteration is not possible<br />

Robust co lection procedures by NZQA certified co lectors<br />

greatly reduce the risk of this occurring<br />

Substitution is most unlikely due to co lection by a trained<br />

co lector and chain of custody requirements<br />

Cannabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of cannabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not blood levels<br />

Tests for THC and metabolites<br />

Passive Inhalation<br />

of Cannabis<br />

Testing wi l not give a positive result at the cut-off levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no possibility<br />

of measuring passive inhalation<br />

Advantages Used extensively A positive result indicates use within a short time prior to<br />

co lection. This gives a stronger indication that the person<br />

was “at risk” at the time of collection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal cha lenge Some drug levels (not cannabis) can be related to<br />

blood levels<br />

Non invasive collection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was at the time of co lection<br />

Witnessed co lection<br />

Application Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

Good for post-incident and post rehabilitation Suitable for use in medico-legal, family and criminal law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contact the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

www.esr.cri.nz<br />

Compari<br />

Urine, Oral<br />

drug test<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2 08 “Procedures for the collection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with scr ening by immunoa say and<br />

confirmation of any positive screen results by ma s<br />

spectrometry before reporting<br />

Laboratory based with scr ening by immunoa say and<br />

confirmation of any positive scr en results by ma s<br />

spectrometry before reporting<br />

Laboratory based with analysis by ma spectrometry<br />

Confirmation only testing available for urine specimens<br />

scr ened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite scr ening is not reliable for ca nabinoids<br />

Cut-o f<br />

Levels/ Target<br />

Concentrations<br />

Cut-o f levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-off levels or target concentrations documented<br />

Cut-o f levels reflect recent, relatively recent o regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for ca nabis “Hours” for ca nabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up to one year<br />

Can be up to thr e w eks after chronic use (i.e: more<br />

than 5 ca nabis cigare tes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

cannabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is po sible but laboratories<br />

and collectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witnessed collection<br />

Adulteration is not possible<br />

Robust co lection procedures by NZQA certified co lectors<br />

greatly reduce the risk of this o cu ring<br />

Substitution is most unlikely due to collection by a trained<br />

collector and chain of custody requirements<br />

Ca nabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of cannabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not blood levels<br />

Tests for THC and metabolites<br />

Pa sive Inhalation<br />

of Ca nabis<br />

Testing wi l not give a positive result at the cut-off levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no po sibility<br />

of measuring pa sive inhalation<br />

Advantages Used extensively A positive result indicates use within a shor time prior to<br />

co lection. This gives a stronger indication tha the person<br />

was “at risk” a the time of collection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal cha lenge Some drug levels (not ca nabis) can be related to<br />

bl od levels<br />

Non invasive co lection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was a the time of collection<br />

Witne sed collection<br />

A plication Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

G od for post-incident and post rehabilitation Suitable for use in medico-legal, family and crimina law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contact the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Urine<br />

drug testing in the<br />

workplace<br />

What does a positive result mean?<br />

A positive result means that the person tested has consumed<br />

drugs recently and has drugs or their metabolites in their<br />

system to a measured level. The measured level is above the<br />

cut-off levels determined by the AS/NZS 4308: 2008 urine<br />

testing standard.<br />

Drug detection times in urine.<br />

The detection times differ for individual drugs but essentially<br />

drugs can be detected in urine from 4 hours and up to 20 days<br />

following use.<br />

Is urine testing the best testing option<br />

for my business?<br />

Urine testing for drugs has been widely used in New Zealand<br />

workplaces for many years. ESR laboratory urine testing is<br />

proven to be a robust and effective testing method when used<br />

in conjunction with a company’s drug testing policy.<br />

Oral Fluid and Hair testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Alcohol<br />

in the workplace<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk on (04) 914 0731<br />

FAQs<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Replace<br />

image<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Comparison of ESR’s<br />

Urine, Oral fluid and Hair<br />

drug testing services<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk<br />

on (04) 914 0731<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Urine<br />

drug testing in the<br />

workplace<br />

What does a positive result mean?<br />

A positive result means that the person tested has consumed<br />

drugs recently and has drugs or their metabolites in their<br />

system to a measured level. The measured level is above the<br />

cut-off levels determined by the AS/NZS 4308: 2008 urine<br />

testing standard.<br />

Drug detection times in urine.<br />

The detection times differ for individual drugs but essentially<br />

drugs can be detected in urine from 4 hours and up to 20 days<br />

following use.<br />

Is urine testing the best testing option<br />

for my business?<br />

Urine testing for drugs has been widely used in New Zealand<br />

workplaces for many years. ESR laboratory urine testing is<br />

proven to be a robust and effective testing method when used<br />

in conjunction with a company’s drug testing policy.<br />

Oral Fluid and Hair testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2 08 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with scr ening by i munoa say and<br />

confirmation of any positive screen results by ma s<br />

spectrometry before reporting<br />

Laboratory based with scr ening by i munoassay and<br />

confirmation of any positive scr en results by mass<br />

spectrometry before reporting<br />

Laboratory based with analysis by ma spectrometry<br />

Confirmation only testing available for urine specimens<br />

screened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite screening is not reliable for ca nabinoids<br />

Cut-o f<br />

Levels/ Target<br />

Concentrations<br />

Cut-off levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-off levels or target concentrations documented<br />

Cut-off levels reflect recent, relatively recent o regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for ca nabis “Hours” for cannabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up t one year<br />

Can be up to three w eks after chronic use (i.e: more<br />

than 5 ca nabis cigare tes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

ca nabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is possible but laboratories<br />

and co lectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witne sed collection<br />

Adulteration is not po sible<br />

Robust co lection procedures by NZQA certified collectors<br />

greatly reduce the risk of this o cu ring<br />

Substitution is most unlikely due to co lection by a trained<br />

collector and chain of custody requirements<br />

Ca nabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of cannabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not bl od levels<br />

Tests for THC and metabolites<br />

Pa sive Inhalation<br />

of Ca nabis<br />

Testing wi l not give a positive result at the cut-o f levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no po sibility<br />

of measuring pa sive inhalation<br />

Advantages Used extensively A positive result indicates use within a shor time prior to<br />

co lection. This gives a stronger indication tha the person<br />

was “at risk” a the time of collection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal challenge Some drug levels (not cannabis) can be related to<br />

bl od levels<br />

Non invasive co lection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was a the time of collection<br />

Witne sed collection<br />

Application Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

G od for post-incident and post rehabilitation Suitable for use in medico-legal, family and crimina law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contac the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Alcohol<br />

in the workplace<br />

For further information,<br />

please contact the<br />

Workplace Drug Testing<br />

Helpdesk on (04) 914 0731<br />

FAQs<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

15 minutes.<br />

Replace<br />

image<br />

FAQ<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the previous<br />

15 minutes.<br />

When can I use alcohol testing in my<br />

workplace?<br />

Alcohol testing is governed by the provisions of your drug<br />

and alcohol testing policy. Alcohol testing can be undertaken<br />

at any time in accordance with the Policy. However, testing<br />

is usually performed randomly, post-incident or for<br />

reasonable cause when alcohol use is suspected.<br />

Do not use if a person has used a breath freshener or other<br />

medicinal formulations containing alcohol in the last<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2008 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with screening by immunoassay and<br />

confirmation of any positive screen results by mass<br />

spectrometry before reporting<br />

Laboratory based with analysis by mass spectrometry<br />

Confirmation only testing available for urine specimens<br />

screened on-site as “not negative”<br />

Detects parent drugs and some metabolites Detects parent drugs and some metabolites<br />

Detects both the parent drug and/or their metabolites Onsite screening is not reliable for cannabinoids<br />

Cut-off<br />

Levels/ Target<br />

Concentrations<br />

Cut-off levels exist and are documented in the Standard Target/nominated concentrations are documented No cut-off levels or target concentrations documented<br />

Cut-off levels reflect recent, relatively recent or regular<br />

use<br />

Target concentrations reflect very recent use of a drug<br />

Drug Detection<br />

Time<br />

“Days” for cannabis “Hours” for cannabis (very dependent on target/<br />

nominated concentrations)<br />

From 7 days up to one year<br />

Can be up to three weeks after chronic use (i.e: more<br />

than 5 cannabis cigarettes/day over a long period)<br />

Target concentrations indicate a detection time for<br />

cannabis use of up to 6 hours and for other drugs up to<br />

24 hours<br />

Adulteration/<br />

Substitution<br />

Adulteration or substitution is possible but laboratories<br />

and co lectors are aware of this and can check for<br />

adulteration<br />

Substitution is difficult as the mouth is checked prior to a<br />

witnessed co lection<br />

Adulteration is not possible<br />

Robust co lection procedures by NZQA certified co lectors<br />

greatly reduce the risk of this occurring<br />

Substitution is most unlikely due to co lection by a trained<br />

co lector and chain of custody requirements<br />

Cannabis Testing Tests for the presence of THC-Acid, the main product<br />

found in the urine after use of THC<br />

Tests for THC, the main active ingredient of cannabis.<br />

Results reflect what is left in the mouth after smoking<br />

and may not blood levels<br />

Tests for THC and metabolites<br />

Passive Inhalation<br />

of Cannabis<br />

Testing will not give a positive result at the cut-off levels<br />

used in the Standard<br />

Should not give a positive result on the target levels Testing for THC metabolites ensures there is no possibility<br />

of measuring passive inhalation<br />

Advantages Used extensively A positive result indicates use within a short time prior to<br />

collection. This gives a stronger indication that the person<br />

was “at risk” at the time of co lection.<br />

Can detect a history of drug use<br />

ESR laboratory testing has held up to legal challenge Some drug levels (not cannabis) can be related to<br />

blood levels<br />

Non invasive collection<br />

Indicates “risk factor” but not how much “at risk” a<br />

person was at the time of collection<br />

Witnessed co lection<br />

Application Used for pre-employment, random, reasonable cause,<br />

post-incident and post rehabilitation<br />

Good for post-incident and post rehabilitation Suitable for use in medico-legal, family and criminal law<br />

cases, rehabilitation management, insurance and some<br />

workplace situations<br />

Comparison of ESR’s Urine, Oral Fluid and Hair drug testing services<br />

For further information, please contact the Workplace Drug Testing Helpdesk on (04) 914 0731<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

Oral Fluid<br />

drug testing in the<br />

workplace<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Is oral fluid testing the best drug testing<br />

option for my business?<br />

The ability to detect the recent use of drugs makes oral fluid<br />

testing an ideal choice for post-incident type testing. Urine and<br />

hair testing options are also available from ESR.<br />

Will recent oral surgery affect the result?<br />

No. Oral surgery will not affect the resulting test in any way.<br />

Is oral fluid a ‘hazardous substance’?<br />

Oral fluid should be treated as a hazardous substance. As a<br />

human body fluid it could contain infectious organisms. Oral<br />

fluid specimens should be handled and treated as if infectious<br />

and capable of transmitting infection. All collection materials<br />

must be disposed of in an appropriate manner.<br />

How do you know it is that drug?<br />

Each sample is first screened to check for the evidence of the<br />

use of the drug classes stated above.<br />

Any presumptive positives are confirmed using a mass<br />

spectrometer, which looks specifically at the chemical structure<br />

of the drugs. This is unique for each drug and allows us to be<br />

certain that we are correctly reporting the presence of a drug.<br />

This means that we know whether the drug is from an over the<br />

counter medicine or illicit drug use.<br />

Does a positive result mean the<br />

individual is impaired?<br />

No. A positive result means the drug has been recently used<br />

but does not provide information on the effects it has had.<br />

FAQs<br />

Hair Testing<br />

for drug use<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

These publications and further<br />

information can be obtained from<br />

the Workplace Drug Testing<br />

helpdesk on (04) 914 0731 or<br />

email wdt@esr.cri.nz<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

Could it be from passive smoking or<br />

ingestion?<br />

There is little scientific information about the effect of<br />

passive ingestion of a drug and the detection of that drug<br />

in hair. It is likely that the exposure would have to be at a<br />

high level and for a prolonged period for it to be detected in<br />

the hair. We also minimise the chance of reporting passive<br />

exposure in the hair by washing the samples before analysing.<br />

How much hair is needed?<br />

The amount of hair needed to test for all the drug classes is<br />

approximately the width of a pencil. This is taken from the<br />

back of the head and does not leave a visible bald patch.<br />

We can use hair from other parts of the body if head hair is<br />

not available. Growth rates are much more variable in other<br />

areas so time periods cannot be estimated.<br />

Oral Fluid and urine testing options are also available from<br />

ESR. A comparison of the three testing options is shown in<br />

the graph below.<br />

www.esr.cri.nz<br />

www.esr.cri.nz<br />

Comparison of ESR’s<br />

Urine, Oral fluid and Hair<br />

drug testing services<br />

Drug testing methods<br />

and their approximate detection periods<br />

1 2 5<br />

Timeline (Days)<br />

10 20 30+ Days<br />

Oral<br />

fluid<br />

Urine<br />

Hair<br />

12−24<br />

hours<br />

Concentration (not to scale)<br />

Cut off levels<br />

Positive results<br />

Negative<br />

results<br />

4 hours<br />

−20 days<br />

Up to 365 days<br />

URINE testing ORAL FLUID testing HAIR testing<br />

Testing Standards AS/NZS 4308:2 08 “Procedures for the co lection,<br />

detection and quantitation of drugs of abuse in urine”<br />

No specific standard for hair testing<br />

Testing Procedure Laboratory based with scr ening by i munoa say and<br />

confirmation of any positive scr en results by ma s<br />

spectrometry before reporting<br />

Laboratory based with scr ening by i munoa say and<br />

confirmation of any positive scr en results by ma s<br />

spectrometry before reporting<br />

Laboratory based with analysis by ma spectrometry<br />

Confirmation only testing available for urine specimens<br />

scr ened on-s


statement of core purpose Outcome 3<br />

Enhance the protection of New Zealand’s foodbased<br />

economy through the management of<br />

food safety risks associated with traded goods<br />

ESR contributes to a healthy, safe and tradable food supply, providing<br />

advice, monitoring and diagnostic services, and food safety research.<br />

We are a major science provider to MAF (Food Safety).<br />

> We continued to develop our capabilities in risk analysis, risk modelling, food<br />

chemistry, microbiology and virology and delivered services to government and food<br />

industry clients. Our international research collaborations, particularly with China and<br />

the European Union, continued.<br />

22 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Foodborne illnesses and food complaints<br />

The rapid and specific detection of pathogens causing human illness is vital for identifying<br />

causes and sources of infections and provides essential information to control foodborne<br />

diseases. ESR undertakes sample testing of suspected foodborne illness outbreaks for the<br />

public health service and MAF.<br />

> We tested clinical, food, water and environmental samples from 222 suspected<br />

foodborne illness episodes.<br />

Identifying Yersinia in food samples<br />

The gastrointestinal illness Yersiniosis is the third most frequently notified foodborne<br />

disease in New Zealand. Until now it has been difficult to test for in food and<br />

other samples. Using Capability Funding we developed tests which can identify the<br />

contaminated foods and the specific strains.<br />

Faster, cheaper testing for Campylobacter and pathogenic E. coli<br />

New ways of strain typing two important foodborne bacteria – Campylobacter and<br />

pathogenic E. coli were developed. ‘P-BIT’, or PCR Binary Typing method, is based on<br />

genome sequences of multiple strains. It provides a rapid, cost-effective typing system<br />

that can be utilised by any lab capable of PCR. Information can be shared easily among<br />

laboratories to help in identifying and responding to outbreaks.<br />

> The methods were published in international journals this year and laboratories in<br />

Poland, Ireland and Belgium are now utilising them.<br />

> Visiting fellow Professor Olivier Vandenberg (Head of the Campylobacter reference<br />

laboratory, Brussels) has commissioned additional research.<br />

> In complementary research, ESR took an existing approach used for detecting<br />

multiple genes in humans and adapted it for use in the detection and P-BIT typing of<br />

Campylobacter and pathogenic E. coli.<br />

> Up to 40 genes can be detected in a single reaction, making both the detection of<br />

multiple pathogens and P-BIT typing faster and cost effective.<br />

> With a Royal Society of New Zealand grant, staff visited a test-kit supplier overseas to<br />

initiate discussions on the commercialisation of this technology.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 23


<strong>Science</strong> and research for government<br />

One of our key roles is providing scientific analysis and advice for food safety regulation<br />

and policy. This year we:<br />

> completed 31 scientific reports for MAF<br />

> delivered food-safety-related reports to other agencies.<br />

The reports covered a range of scientific advice and research, including risk analysis and<br />

modelling, food contamination, foodborne diseases, chemical contaminants and dietary<br />

health. <strong>Report</strong>s are made available on the Government’s food safety website<br />

www.foodsafety.govt.nz and include:<br />

> annual report concerning foodborne diseases in New Zealand 2010<br />

> Campylobacter spp. in uncooked retail chicken meats<br />

> Campylobacter transmission: collaborative research.<br />

Total Diet Survey<br />

One of our major projects for MAF is planning, managing and undertaking the Total Diet<br />

Survey every five years. About 1400 kilograms of food are collected, prepared and sampled<br />

to find out what average New Zealanders eat. The Survey provides a scientific analysis<br />

of our total diet, broken into age and gender groups, and estimates dietary exposure to<br />

chemical residues, contaminants and selected nutrients. This year we completed the 2006-<br />

<strong>2011</strong> survey and delivered comprehensive reports to MAF.<br />

> We have also been contracted to provide services for the Australian equivalent in <strong>2011</strong>.<br />

24 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


<strong>Environmental</strong> and food virology<br />

ESR provides specialist services for the detection and identification of enteric viruses in<br />

environmental and food samples, including shellfish, fresh produce, sewage, sludge and<br />

environmental waters. We test for viruses implicated in outbreaks and provide analytical<br />

advice for local authorities, public health services, industry and food safety agencies. We<br />

are the only laboratory in the Pacific region to offer specialist virus testing.<br />

> We saw a significant increase in demand for the detection and monitoring of norovirus<br />

in shellfish, environmental waters and sewage, particularly from local authorities.<br />

> We undertook research for the Department of Health, Victoria, Australia, in relation<br />

to the survival of the hepatitis A virus on fresh and semi-dried tomatoes that caused<br />

a major outbreak. We have been re-contracted in the coming year to continue the<br />

development of the most promising control strategy identified.<br />

Seafood safety research<br />

Current testing methods can’t discriminate between infectious and non-infectious<br />

noroviruses, so we’re developing a new test to identify infectious noroviruses in shellfish<br />

and other foods as part of an MSI research programme. <strong>Research</strong> is also underway to find<br />

a norovirus-resistant shellfish by investigating the binding of noroviruses to shellfish.<br />

We’re evaluating a low-cost material to catch enteric viruses in seawater and freshwater<br />

and have developed specific virus tests to distinguish between human and animal faecal<br />

contamination. These tests are available for tracking virus pollution sources.<br />

Virucidals<br />

Capability Funded research continued into investigating how effective hand sanitisers and<br />

other virucidals are at killing viruses. A commercial service will be offered from early 2012.<br />

Biocontrol research<br />

Biocontrols harness the ability of naturally occuring agents that can damage or destroy<br />

pathogens. Our research is focusing on using bacteriophages (phages), to reduce meat<br />

contamination from common food pathogens. We consult and involve the meat industry<br />

in this MSI-funded research programme.<br />

> In November 2010 we hosted an Ministry of Foreign Affairs and Trade-funded Food<br />

Safety China relationship-building workshop on ‘Developing resources for food<br />

safety biocontrol’ that also involved colleagues from the Chinese Cereals and Oils<br />

Association.<br />

> A website was established to provide information relevant to the regulatory aspects of<br />

biocontrol of foodborne pathogens.<br />

IMPACT<br />

As lead agency, we continued research on the MSI-funded IMPACT project with<br />

Massey University and Ag<strong>Research</strong>. IMPACT stands for IMproved PAthogen Control<br />

Technologies. The six-year project is funded by MSI and will continue until 2013.<br />

IMPACT aims to eliminate or substantially reduce key pathogens in exported meat using<br />

natural, organic methods, compatible with New Zealand’s ‘clean and green’ image.<br />

Biofilms<br />

We have been investigating the production of a ‘clean green’ sanitiser for the food industry<br />

that is capable of decontaminating biofilms. Biofilms form when bacteria adhere to<br />

surfaces in some form of watery environment and pose a potential source of reinfection in<br />

industrial food processing and hospital environments.<br />

> A collaboration was established with China’s Jiangsu Academy of Agricultural <strong>Science</strong>s<br />

to assist in the development of a specific enzyme solution that could destroy Listeria<br />

monocytogenes in soy milk.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 25


Collaborating with the EU on food safety<br />

ESR is involved in a major EU-funded food safety project – MoniQa. We are leading an<br />

international Campylobacter project evaluating test methodology. Our in-house results on<br />

six PCR assays for Campylobacter demonstrate the need for such a process.<br />

> In collaboration with United Kingdom scientists we published a paper on the impacts<br />

of climate change on the formation, distribution and uptake in food of environmental<br />

contaminants.<br />

> We hosted an international MoniQA Workshop ‘Assessing impacts of chemical<br />

contaminants in foods and feedstuffs’. Attendees included representatives from<br />

government agencies and universities, from New Zealand and overseas.<br />

Allergen testing<br />

Faster, cheaper laboratory methods for detecting allergens in foods were developed this<br />

year. Until now, testing allergens in foods has relied on labour-intensive analysis kits.<br />

The new method utilises a machine called an LCMS (liquid chromatography–mass<br />

spectrometry), which can quickly analyse a large number of samples, including highly<br />

processed and manufactured foods.<br />

> Methods for detecting wheat allergens (gluten) were developed. These are being<br />

validated in-house, with routine laboratory analysis expected to be available by<br />

early 2012.<br />

> Through the MoniQA network we are collaborating with other laboratories working on<br />

similar methods for peanut, dairy and egg allergen detection.<br />

Keeping freshly grown fruit and veg safe<br />

With Catalyst® R&D, ESR is involved in a MAF-commissioned research project to help<br />

local vegetable and fruit growers keep producing safe food and avoid problems that have<br />

occurred overseas. It will enable guidance to be given to growers on how to produce food<br />

as safely as possible.<br />

Future foods<br />

We are midway through an MSI-funded research project investigating social, cultural and<br />

consumer responses to a range of emerging future food technologies.<br />

> We have had local industry feedback that the project is providing a significant new<br />

approach, beyond traditional market research, to understand the drivers of consumer<br />

acceptance of novel food technologies.<br />

> There is considerable international interest in the research.<br />

> ESR was subcontracted to provide food safety advice, including risk profiling and<br />

analysis as part of a three-year Lincoln University MSI-funded project on a novel<br />

process to produce a new snack food.<br />

26 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


statement of core purpose Outcome 4<br />

Improve the safety of freshwater and<br />

groundwater resources for human use and the<br />

safer use of biowastes<br />

ESR provides scientific advice and expertise for the management of<br />

drinking, recreational and waste water. As principal science advisor<br />

to the Ministry of Health, we provide advice supporting health<br />

and environmental public policy, action and information systems<br />

management.<br />

ESR has significant groundwater, wastewater and biosolids research capability and we are<br />

growing our knowledge in the greywater area. We are also improving microbiological and<br />

molecular techniques to solve environmental health issues.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 27


Drinking water<br />

ESR manages and produces a range of data and information vital to ensure the safe supply<br />

of New Zealand’s drinking water.<br />

On behalf of the Ministry of Health, we manage Water Information New Zealand<br />

(WINZ), a national database providing up-to-date national water supply information<br />

required for drinking-water quality management. WINZ meets the specific needs of local<br />

authorities to manage their drinking-water supplies.<br />

> ESR maintains a website (www.drinkingwater.org.nz) where WINZ and other<br />

information about water supply management is available.<br />

We undertook the annual review of drinking water, which describes the microbiological<br />

and chemical qualities of New Zealand’s drinking-water supplies. With a complete record<br />

from the early 1990s, it shows water quality and supply compliance over time.<br />

> We produced the annual register of community drinking-water supplies.<br />

Scientific water advice<br />

We provide on-demand advice to the Ministry of Health and public health units. Public<br />

health units request advice on a range of issues including sewage treatment, contaminated<br />

sites, water quality and chemical safety. A component of this work involves assessing the<br />

environmental health effects of resource consents involving contaminant discharges.<br />

> We also provided training courses to drinking-water assessors nationwide.<br />

Groundwater<br />

Groundwater is an important source of drinking and stock water, crop<br />

irrigation and industrial applications. Intensive agricultural and domestic<br />

sewage disposal can cause groundwater contamination from pesticides,<br />

animal waste and waterborne diseases. ESR has led an integrated<br />

groundwater research programme since 1993. Each year the programme<br />

provides important knowledge to government, local authorities,<br />

representatives of specific activity groups, and water managers.<br />

The four-yearly survey of pesticides was completed this year, the sixth<br />

survey since 1990. The results have proved so valuable for monitoring<br />

groundwater quality that regional councils have taken over funding from<br />

MSI and are incorporating the results into their ‘state of the environment’<br />

reporting.<br />

Around 20% of wells sampled have detectable pesticides present but at<br />

concentrations that are much lower than drinking-water standards. Pesticide<br />

concentrations are trending downward slightly, and most wells show that<br />

groundwater quality is meeting acceptable limits for drinking water.<br />

28 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Groundwater assimilative capacity<br />

A major new MSI-funded groundwater research programme of $1.5m per annum<br />

in partnership with Lincoln Ventures Limited began this year. It brings water quality<br />

management and land-use planning together by improving the scientific understanding<br />

of the linkage between land use, the subsurface environment and groundwater.<br />

> A key outcome is the development of tools to enable regional councils to achieve<br />

groundwater quality targets.<br />

> The research features collaboration with the United States Air Force Institute of<br />

Technology, Flinders University in Australia, the Commonwealth Scientific and<br />

Industrial <strong>Research</strong> Organisation (CSIRO) in Brisbane, and the University of<br />

California. New Zealand partners include Waikato Regional Council, Environment<br />

Canterbury and Environment Southland, which are supporting the research with cash<br />

co-funding and in-kind support this year.<br />

Clean water productive land research<br />

A new three-year MSI-funded research project began in October 2010. Led by<br />

Ag<strong>Research</strong>, it includes ESR, Landcare <strong>Research</strong> and the National Institute of Water and<br />

Atmospheric <strong>Research</strong> (NIWA). The research will enable rural industries and central and<br />

regional government to predict water quality contaminant loads (nutrients, sediment<br />

and faecal microbes) to surface water across space and time. The suggestion is that 80%<br />

of water contaminants come from 20% of the land. If these critical source areas can be<br />

identified, cost-effective mitigation measures can be implemented.<br />

> ESR research will focus on understanding contaminant sources and pathways at the<br />

interface between land and water.<br />

Tracking viruses through groundwater<br />

The Marsden Fund is supporting an ESR-led research project to make and test how mock<br />

viruses travel into groundwater. Little is known about the behaviour of viruses and other<br />

pathogens in groundwater, so ESR scientists are developing new tools to investigate how<br />

disease-causing viruses travel through aquifers. Real viruses can’t be used in field studies,<br />

so harmless surrogate nano-beads, altered to behave like real viruses, will be used to track<br />

what happens to them in aquifers.<br />

> The three-year research project is being undertaken in collaboration with the University<br />

of Canterbury and Victoria University of Wellington.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 29


Faecal source tracking<br />

ESR has pioneered research to identify whether faecal contamination of the environment<br />

is from human, animal or other sources. To transfer this new knowledge into science<br />

delivery we have purchased a new instrument that enables a high throughput of samples<br />

for analysis, more efficient processing of data and high-quality results.<br />

> This new service was used by regional and local authorities to identify leaking septic<br />

tanks, check stormwater drainage systems and investigate river contamination linked to<br />

dairy farm runoff.<br />

Water in the Pacific<br />

Since 1999 ESR has supported the Secretariat of the Pacific Community (SPC) and the<br />

World Health Organization with Pacific regional consultation and action plan preparation<br />

for wastewater management. This year we had input to the presentations given to the<br />

upcoming Pacific Island Forum leaders’ meeting, the Asia Pacific Water summit and the<br />

World Water Forum.<br />

> In 2010 we also took up leadership of an annual programme of monitoring and<br />

evaluation for an SPC division’s water and sanitation work programme.<br />

> Drinking-water safety training, advice and development delivery continued with<br />

the New Caledonian Government. ESR had also been contracted previously to help<br />

identify drinking-water projects for EU funding. These projects were funded this year<br />

and ESR’s involvement is continuing.<br />

> In Fiji we continued to work in collaboration with NIWA and the University of the<br />

South Pacific to provide public health risk assessments and health impact expertise<br />

for NZ Aid-funded projects. Our role has a specific focus on sustainable community<br />

drinking-water and wastewater treatment solutions for coastal Fijian villages. This work<br />

has led to the preparation of a major project proposal, which has been funded for the<br />

<strong>2011</strong>-2012 financial year through the NZ Aid State Sector Development Partnerships<br />

Fund.<br />

> We also investigated offshore water management opportunities in Bahrain and China<br />

in association with other New Zealand companies.<br />

30 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Biosensors<br />

A biosensor research project run in partnership with Victoria University concluded this<br />

year. It explored the potential for developing rapid and cost-effective tests for chemical<br />

toxins or biological activities based on the response of yeast as a biosensor. Proof of<br />

concept was established for a reporter gene biosensor for copper. Competitive growth<br />

biosensors for 1080 were developed and can detect as little as 1µM 1080. Yeast biosensor<br />

strains for the detection of saxitoxin (a marine biotoxin that has significant economic and<br />

health consequences worldwide) were also discovered.<br />

Biowastes programme<br />

ESR is the lead organisation for the MSI-funded biowastes research programme. The<br />

partnership of ESR, Scion and Landcare <strong>Research</strong> together with other collaborators<br />

integrates all of New Zealand’s biosolids (sewage sludge) research. The team is currently<br />

focused on the implementation of biosolids solutions in two regions, Taupō and Kaikōura.<br />

The research will provide information and recommendations for regional land-use<br />

planning, national guidelines and policy directions.<br />

Assessing the impacts of chemical cocktails on the soil ecosystem<br />

Another focus of the programme is to understand what happens to mixtures of microcontaminants<br />

(metals and organic contaminants) when they interact with each other and<br />

with soil. It is now recognised that the additive effects from multiple chemicals can result<br />

in a combined effect greater than the sum of the individual effects. This year we started<br />

analysing historically contaminated soils to determine the impacts of specific metals and<br />

organic mixtures.<br />

Community case study<br />

Studies in Kaikōura and Mokai, near Taupō, are supporting a shared-learning process for<br />

end-users, Māori and other stakeholders to develop viable strategies for biowaste reuse.<br />

In collaboration with Māori research partner Te Rūnanga o Kaikōura and other<br />

organisations, researchers are helping the Kaikōura District Council and community to<br />

decide on the most appropriate way of reusing or managing stockpiled biosolids before a<br />

consent runs out in 2016.<br />

> Two hui were held with a range of stakeholders to assist with developing options<br />

for the reuse or management of the stockpiled biosolids. Further research and<br />

investigations into potential options are underway.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 31


Human resources<br />

The environment in which ESR operates continues to change. We<br />

have implemented a range of initiatives to adapt our culture to<br />

the new environment and employees are actively involved in all of<br />

them.<br />

Employee engagement<br />

Our Culture and Engagement survey has shown us that we have satisfactory levels of<br />

employee engagement – 58% engaged compared with world-class companies rating<br />

around 63%. Staff workgroups have been developing action plans to identify and<br />

implement improvements in areas highlighted by our survey and values workshops.<br />

The action plans align with our strategic human resources initiatives in maintaining our<br />

position as a good employer and exceptional organisation.<br />

Staffing<br />

ESR has 327 FTE staff. We are working to resume normal staff turnover trends<br />

following the impacts of the recession. There were no redundancies during the year, but<br />

process efficiencies, and natural attrition reduced the number of FTEs.<br />

Workforce diversity<br />

ESR is proud to have a very diverse and well balanced workforce. Almost 67.5% of the<br />

workforce are women and around 31% of the workforce are under the age of 40, which<br />

underpins succession planning.<br />

Learning and development<br />

A new learning and development framework has been created with our existing best<br />

practice talent management process, and a new performance management process will<br />

enable us to continue to develop key capabilities and progress science careers.<br />

Staff turnover and recruitment<br />

This year we lost a number of staff through a mixture of retirement, migration and<br />

career shifts.<br />

> Total staff turnover (12-month rolling average) was 12.4%, with science staff 15.4%<br />

and support 8.0%.<br />

Health and safety<br />

ESR provides all staff with comprehensive guidelines, training, mentoring and support<br />

to ensure their health and wellbeing at work. We foster continual improvements for our<br />

health and safety culture. Staff and the PSA (New Zealand Public Service Association)<br />

provide regular input through site-based Health and Safety Committees.<br />

We have maintained tertiary status in the ACC Workplace Safety Management Practices<br />

programme, reflecting our best practice framework and our culture of continual<br />

improvement.<br />

Good employer<br />

ESR is very proud of its reputation as a good employer. The flexibility we offer staff<br />

and our core value of Valuing People supported our staff in Christchurch during a very<br />

difficult year with the continual earthquakes.<br />

32 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


<strong>Research</strong><br />

After many years of increasing research activity, 2010-<strong>2011</strong> was a real challenge. ESR led<br />

and submitted 46 research bids to research investors and was a significant collaborator<br />

in eight others. However, ESR did not meet the research revenue stretch target of<br />

$12,918,000. A key reason was MSI not holding a contestable bidding round.<br />

ESR research funding<br />

15,000<br />

12,000<br />

9000<br />

8065<br />

9424<br />

12,918<br />

12,308<br />

11,517<br />

10,555<br />

10,379<br />

6000<br />

4744<br />

3000<br />

Target funding (2010/13 Strategic Plan)<br />

0<br />

2004<br />

2005 2006 2007 2008 2009 2010/11<br />

Contracted funding<br />

ESR investment in research<br />

The Capability Fund was allocated to the research projects indicated in the 2010 SCI and<br />

the achievements are shown on page 35. ESR is especially proud of the rapid pathway<br />

from research through evaluation to implementation into casework of the new mRNA<br />

technique, which is able to distinguish the body fluid type.<br />

The ESR SCP clearly defines four outcomes to which ESR will contribute. The allocation<br />

of the 2010-<strong>2011</strong> Capability Fund has been retrospectively mapped to these outcomes<br />

and shown in the pie chart.<br />

<strong>Science</strong> communication for MSI<br />

The ESR social systems group secured a tender from MSI to improve the return on<br />

science investment by increasing information flow from scientists to users of science<br />

information.<br />

Key findings indicate that many of the incentives and constraints identified overseas<br />

are relevant for New Zealand scientists. Differences between CRIs and universities,<br />

such as commercial orientation, intellectual freedom and intellectual property rights,<br />

are also factors.<br />

Capability fund allocation<br />

by outcome<br />

16%<br />

18%<br />

40%<br />

26%<br />

Outcome 1 – Health<br />

Outcome 2 – Forensic<br />

Outcome 3 – Food<br />

Outcome 4 – <strong>Environmental</strong><br />

Total Capability Funds: $5.8m<br />

15000<br />

12000<br />

11517<br />

12415<br />

12918<br />

11344<br />

10379<br />

9000<br />

9424<br />

8065<br />

6000<br />

4744<br />

3000<br />

0<br />

2004<br />

2005 2006 2007 2008 2009 2010/11<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 33


Forging international collaborations<br />

ESR continued to support an awards programme to forge close international<br />

collaborations and bring innovation and new knowledge to ESR.<br />

The ESR International Fellowships are awarded to eminent scientists to enable them to<br />

spend time with their ESR hosts discussing new developments and future collaborations.<br />

The six Fellows who spent time with ESR were:<br />

Professor Steven Gorelick is a Professor of Earth <strong>Science</strong>s at Stanford University,<br />

California, USA.<br />

Dr Roland Poms is the Chief Executive of the International Association for Cereal<br />

<strong>Science</strong> & Technology in Vienna, Austria and Professor of the University of Natural<br />

Resources and Life <strong>Science</strong>s in Vienna.<br />

Professor Thomas Briese is an Associate Professor at the Clinical Epidemiology<br />

Center for Infection and Immunity in the Mailman School of Public Health, Columbia<br />

University, New York, USA.<br />

Professor Robin Williams is a Professor of Forensic <strong>Science</strong> Studies at the<br />

Northumbria University Centre for Forensic <strong>Science</strong> in the UK and also Professor<br />

Emeritus of Sociology at the Durham University School of Applied Social <strong>Science</strong>s.<br />

Professor Adrian Linacre holds the South Australia Justice Chair in Forensic<br />

<strong>Science</strong> and Emerging DNA Technologies at Flinders University, South Australia.<br />

Dr David Baldwin is the Director of the Midwest Forensics Resource Center at Ames<br />

Laboratory, Iowa, USA.<br />

Information management<br />

We will:<br />

> enhance our operating information and communication technology (ICT) structures<br />

to deliver timely and quality information for our clients<br />

> establish enabling technologies that are intuitive and innovative will improve efficiency<br />

and business effectiveness<br />

> provide new information streams from existing and new data sources, enabling growth<br />

and marketing opportunities.<br />

A major investment was made to replace the laboratory information management systems<br />

(LIMS) used by all laboratory operations of the <strong>Environmental</strong> Health and Forensic<br />

business groups and consolidate them into a single LIMS platform. The consolidation<br />

of 13 labs into one single platform will go a long way to towards achieving efficiencies<br />

by effectively reducing costs in ongoing maintenance and support through providing a<br />

centralised, supported system. However, there are further benefits that can be achieved<br />

by providing extended business systems capabilities to our clients. The Workplace Drug<br />

Testing laboratory operation was the first recipient of the new LIMS, at the end of June<br />

<strong>2011</strong>. Further deployments will occur throughout the <strong>2011</strong>-2012 financial year.<br />

Other information management developments including the establishment of an<br />

enterprise data warehouse. This will allow the implementation of a single set of effective<br />

business intelligence tools to:<br />

> enable information to be used as a decision support tool<br />

> allow ESR to expose the data to multiple audiences in a controlled way<br />

> improve ESR’s ability to deliver meaningful information to people when and where<br />

they need it.<br />

All these investments are designed to improve the integration and consolidation of<br />

our ‘backbone’ information management systems and processes to deliver operational<br />

efficiencies and to provide the agility that ESR requires to adapt to changes in legislation<br />

and client demand. It also provides the opportunity to build new products and services<br />

using online and digital technologies.<br />

34 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Capability Fund – Priorities for investment<br />

A: Existing capabilities [maintain and enhance] – 60% of total<br />

Capability Areas of activity 2010/11 forecast Achievement<br />

Human<br />

biosecurity<br />

and disease<br />

surveillance<br />

Food safety<br />

Develop research<br />

capability and intelligent<br />

systems to underpin<br />

service delivery, with<br />

particular foci on<br />

biosecurity, enhanced<br />

detection and response<br />

to infectious diseases,<br />

and the impacts of<br />

climate change on<br />

health.<br />

Develop intelligent<br />

systems, molecular tools<br />

and risk assessment<br />

techniques that solve<br />

problems for clients.<br />

Establish nextgeneration<br />

pathogen<br />

identification system<br />

and biosensors and<br />

biomarkers for health.<br />

Maximise PCR using<br />

MPLA and implement<br />

EAT_FOOD<br />

methodology.<br />

Next-generation sequencing used to identify novel viruses<br />

and bacteria in several test cases and links enhanced with<br />

Columbia University, which has pioneered this approach.<br />

Successful respiratory disease study using multiplex<br />

detection of 28 common pathogens. Proteomic and<br />

genomic capabilities are revealing why some meningococcal<br />

strains are invasive. Identified candidate metastasis<br />

biomarkers for colorectal cancer with the Wakefield<br />

Biomedical <strong>Research</strong> Unit at Otago Medical School. Work<br />

continuing on cancer prognosis and diagnosis biomarkers.<br />

Testing of MPLA probes was successful and the project was<br />

aided by an International Mobility Fund award (The Royal<br />

Society of New Zealand) for collaboration with research<br />

partners in Belgium and the Netherlands. Techniques<br />

developed in EAT_FOOD have been applied to exposure<br />

estimates for aflatoxins for MAF.<br />

Forensic science<br />

Develop smarter<br />

forensic techniques and<br />

use new technology to<br />

provide more efficient<br />

and effective service<br />

delivery.<br />

Focus on techniques<br />

and technologies to<br />

assist with blood spatter<br />

analysis, crime scene<br />

assessments, drug testing<br />

in hair and the use of<br />

mRNA in casework.<br />

Novel techniques for modelling ballistic injury and blood<br />

spatter developed and options for technology transfer via a<br />

dedicated website underway. The new mRNA method for<br />

identifying specific body fluids has been operationalised<br />

for routine use in casework; further markers have also been<br />

identified. Laser microdissection of sperm from mixed cell<br />

samples implemented into sexual assault casework analysis.<br />

Drug testing using hair to show historical drug exposures<br />

during hair growth is now offered as a new service.<br />

B: New and emerging capabilities – 30% of total<br />

Capability Areas of activity 2010/11 forecast Achievement<br />

Health<br />

indicators<br />

and biosensor<br />

development<br />

Microbial<br />

and chemical<br />

forensics<br />

platform –<br />

ongoing<br />

Use envirogenomics<br />

and proteomics<br />

capabilities to develop<br />

targeted biomarkers and<br />

biosensors.<br />

CBRE (chemical,<br />

biological, radiological<br />

and explosive) science<br />

– undertake research<br />

to enable the rapid<br />

identification of<br />

microbes and chemicals,<br />

and chain of custody<br />

that underpins NCBID.<br />

Identify and compete<br />

for external research<br />

and service delivery<br />

opportunities to<br />

progressively replace<br />

Capability Funding.<br />

Negotiate new service<br />

delivery with clients.<br />

A chemical marker of tobacco addictiveness has been<br />

studied. External funds received from the Wellington<br />

Medical <strong>Research</strong> Foundation and the End Smoking Trust.<br />

ESR part of a successful Health <strong>Research</strong> Council tobacco<br />

cessation research grant.<br />

Yeast biosensors for copper and 1080 have been developed<br />

and tested but a decision was made to cease further work<br />

in this area. Health <strong>Research</strong> Council and Marsden<br />

Funds now support significant meningococcal research.<br />

Bioinfomatics expertise is being applied across ESR.<br />

The importance of this capability to NZ is understood<br />

by key parties.Negotiation with Department of Prime<br />

Minister and Cabinet, Fire Service, New Zealand Police<br />

and Ministry of Health undertaken during the year with a<br />

commitment made to fund this capability, but no contract<br />

has been signed to date.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 35


Capability Areas of activity 2010/11 forecast Achievement<br />

Forensic<br />

research<br />

platform –<br />

ongoing<br />

Undertake innovative<br />

‘beyond DNA’ forensic<br />

research.<br />

Continue to build<br />

research capability<br />

in applied molecular<br />

biology leading<br />

to innovation in<br />

forensic service<br />

delivery. Consolidate<br />

international reputation<br />

in blood spatter analysis<br />

using new technologies.<br />

Novel technologies continue to be researched with a view<br />

to providing additional forensic capability and more<br />

efficient, effective and essential service delivery to clients.<br />

Development and delivery of a fluid dynamics blood<br />

pattern analysis course in New Zealand, Canada and USA.<br />

Service science<br />

platform<br />

Develop new research<br />

capability in service<br />

science.<br />

Lead new international<br />

methodological<br />

developments in service<br />

science research using<br />

practical projects in<br />

collaboration with<br />

stakeholders.<br />

A new relationship has been established with the<br />

Canterbury Earthquake Recovery Authority (CERA) on<br />

innovative decision-making and engagement services. A<br />

new project with the Ministry of Justice will assist it to<br />

measure and monitor justice outcomes. Continued the<br />

relationship with New Zealand Police on community<br />

engagement. The risk and decision-making project<br />

has covered a number of areas, including Canterbury<br />

earthquake risk communication. A health services project<br />

has been developed with Canterbury DHB, Partnership<br />

PHO and Pegasus Health.<br />

<strong>Environmental</strong><br />

health<br />

Take new directions in<br />

the biocontrol of foodborne<br />

pathogens.<br />

Undertake research<br />

on Yersiniosis in New<br />

Zealand.<br />

Clinical laboratory methods developed for identification<br />

of Yersiniosis. Improved typing methods to be adopted by<br />

the enteric reference laboratory at ESR. Biofilm research<br />

capability established. Fast and cost-effective ‘P-BIT’ enteric<br />

pathogen typing method, which also assesses pathogenicity,<br />

has been published and is being used internationally.<br />

C: Over the horizon [discovery and creative insight activity] –<br />

10% of total<br />

potential<br />

Capability Areas of activity 2010/11 forecast Achievement<br />

New technology<br />

– Futurewatch<br />

Combine MoRST<br />

and ESR Futurewatch<br />

programmes with a view<br />

to identifying new or<br />

disruptive technologies.<br />

Maintain a watching<br />

brief on new<br />

technologies useful for<br />

ESR activities, present<br />

and future. Take action<br />

as required.<br />

Relevant staff informed of new technologies. Ongoing<br />

subcontract to Industrial <strong>Research</strong> Limited for<br />

nanotechnology project.<br />

36 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Financial section<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 37


Non-financial performance measures<br />

Actual<br />

Target<br />

Benefit to New Zealand<br />

1. Value of public good services provided in New Zealand ($m) 45 50<br />

2. Invitations or elections to serve on national or international<br />

scientific agencies, boards or advisory committees 19 50<br />

<strong>Science</strong> Output<br />

1. Papers accepted for publication in international externally refereed<br />

scientific journals, series or books 67 95<br />

2. Papers in local, internally or editor-refereed journals, series or books 8 10<br />

3. Invited keynote and plenary presentations – costs paid in full or part 22 30<br />

4. Conference papers and abstracts 103 100<br />

5. <strong>Research</strong> monographs or books – –<br />

6. Scientific and technical reports 98 150<br />

7. Submissions for research and development funding 47 40<br />

Application and promotion of science<br />

1. Staff involvement in conferences, workshops, training sessions or hui<br />

– Number of events 192 250<br />

– Number of attendees 389 350<br />

2. Availability and use of ESR Culture Collection 1691 1800<br />

3. Number of Tech NZ contracts – 1<br />

4. Support for New Zealand <strong>Science</strong> system:<br />

Number of bids to funding agencies and papers for scientific journals refereed 120 200<br />

Number of MSc and PhD students supervised. Number of MSc and PhD theses<br />

externally examined<br />

5. Number of science-promoting media exposure events 164 150<br />

6. Number of science-related talks to schools, community groups and<br />

service clubs 11 40<br />

Good employer<br />

1. Staff turnover<br />

% of total staff (excluding redundancies and fixed-term contracts) 12 10<br />

2. Number of work days lost through workplace accidents<br />

Number of workdays lost as a % of total working days


Key financial performance measures<br />

Year Target Year<br />

ended<br />

ended<br />

30 June <strong>2011</strong> 30 June 2010<br />

Revenue, $M 51.4 53.5 53.5<br />

EBIT* margin, % 7.0 7.2 8.0<br />

Return (NPAT**) on equity % 9.5 7.6 -1.6<br />

Return (EBIT) on assets, % 6.8 8.3 8.5<br />

Acid test, ratio 1.7 1.4 1.5<br />

Equity ratio 64.0 78.5 68.6<br />

Gearing 0.8 – 0.9<br />

Interest cover – – –<br />

<strong>Annual</strong>ised Revenue/FTE, $’000s (including casual staff) 158.2 150.3 157.8<br />

* Earnings (Surplus) before Interest and Taxation<br />

** Net Profit (Surplus) After Taxation<br />

Statement of responsibility<br />

We certify that the Company has operated in accordance with the principles of the Crown <strong>Research</strong> Institutes<br />

Act 1992 and Companies Act 1993. The Company has also complied with all statutory environmental<br />

obligations.<br />

We acknowledge responsibility for the preparation of these financial statements and for the judgements used<br />

therein.<br />

Internal control procedures are considered to be sufficient to provide a reasonable assurance as to the integrity<br />

and reliability of the financial reports.<br />

In our opinion these financial statements fairly reflect the financial position and operations of the Institute of<br />

<strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited (ESR) for the year ended 30 June <strong>2011</strong>.<br />

Dr Susan Macken Elizabeth Hickey Dr Fiona Thomson-Carter<br />

Chair Director Chief Executive Officer<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 39


General disclosures<br />

<strong>Annual</strong> report<br />

The directors and management of ESR present the report of the Institute for the year ended 30 June <strong>2011</strong>.<br />

Financial statements<br />

The financial statements for ESR, including the report of the auditor, for the year ended 30 June <strong>2011</strong> follow<br />

this report from page 42.<br />

PricewaterhouseCoopers has indicated its willingness to continue in office as auditor on behalf of the Controller<br />

and Auditor-General. Details of the auditor’s remuneration and expenses are disclosed in note 2 to the financial<br />

statements.<br />

Remuneration of directors<br />

The directors who held office in the period of this report and their total remuneration and other benefits were:<br />

Dr Susan Macken $46,000<br />

Ross Peat $28,750<br />

Elizabeth Hickey $23,250<br />

Tahu Potiki $23,000<br />

Professor William Denny $23,000<br />

Dr Judith Johnston $23,000<br />

Patricia Schnauer $23,000<br />

$190,000<br />

Disclosures of interest by directors<br />

General Disclosures<br />

The following are particulars of general disclosures of interest given during the year by the directors of the<br />

Company pursuant to section 140 (2) of the Companies Act 1993:<br />

Dr Susan Macken (Chair)<br />

Independent non-executive Director, Bank of New Zealand<br />

Director, Fertility Associates<br />

Director, Auckland Regional Amenities Funding Board<br />

Managing Director, STG Ltd<br />

Director, Blossom Bear Ltd<br />

Non-executive Director, New Zealand Treasury<br />

Director, Ultimate Care Group<br />

Ross Peat (Deputy Chair)<br />

Director, Healthsoft Ltd<br />

Director, Healthsoft Australia Ltd<br />

Director, Kinopta Ltd<br />

Director, YuVu Ltd<br />

Director, KlickEx Trading Ltd<br />

Director, KlickEx Corporation Ltd<br />

Member, Digital Auckland Working Party<br />

Member, University of Otago Business School Advisory Board<br />

Trustee, Hi Tech Trust<br />

Dr Judith Johnston<br />

Director, Petone Medical Centre Ltd<br />

Shareholder, Judith Johnston Ltd<br />

Clients of Judith Johnston Ltd<br />

Ministry of Education<br />

Maritime New Zealand<br />

Tertiary Education Commission<br />

State Services Commission<br />

IRD Risk & Assurance Committee<br />

Parliamentary Council Office Risk & Audit Committee<br />

New Zealand Qualifications Authority<br />

Open Polytechnic of New Zealand<br />

Department of Internal Affairs<br />

40 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Elizabeth Hickey<br />

Director, Southern Cross Health Group<br />

Trustee, Southern Cross Health Trust<br />

Director, New Zealand Institute of Chartered Accountants<br />

Co-opted member of Audit & Risk Committee, ASB Community Trust<br />

Trustee, Sight Loss Services Charitable Trust Board<br />

Tahu Leslie Potiki<br />

Board Member, Southern District Health Board<br />

Councillor, New Zealand Council for Educational <strong>Research</strong><br />

Director, Māori Television Service<br />

Elected Representative, Te Runanga o Ngāi Tahu<br />

Trustee, Ngāi Tahu Charitable Trust<br />

Board Member, Relationship Services New Zealand<br />

Director, Arataki Associates Ltd<br />

Patricia Schnauer<br />

Trustee, North Shore Hospice<br />

Trustee, North Harbour Stadium Trust<br />

Director, MILife Trustee Ltd<br />

Director, Millaw Services Ltd<br />

Professor William (Bill) Denny<br />

Director, Auckland Cancer Society <strong>Research</strong> Centre, University of Auckland<br />

Head, Scientific Advisory Committee, Australian Cancer <strong>Research</strong> Foundation Drug Discovery Centre, Sydney<br />

Member, Scientific Advisory Group, Australian Cooperative <strong>Research</strong> Centre for Cancer Therapeutics,<br />

Melbourne<br />

Member, Ministry of Health/Health <strong>Research</strong> Council Steering Committee for Cancer <strong>Research</strong> Partnership<br />

Member, Management Group, Maurice Wilkins Centre for Molecular Bioscience, University of Auckland<br />

Member, Senior Management Team, Cancer Society Auckland<br />

Shareholder, Proacta Inc, San Diego<br />

Shareholder, Pathway Therapeutics Ltd, San Francisco<br />

Directors’ interests<br />

No director held any interest in the shares of the Institute. The Institute has funding contracts with the<br />

Marsden Fund and the Foundation for <strong>Research</strong>, <strong>Science</strong> and Technology, which are negotiated at arm’s length<br />

with appropriate directors’ interests being declared. Except for these contracts no material contracts involving<br />

directors’ interests were entered into during, or subsequent to, the period covered by this report.<br />

Remuneration<br />

Total remuneration in respect of employees paid above $100,000 was as follows:<br />

Remuneration range<br />

No. of staff<br />

$100,000 – $109,999 14<br />

$110,000 – $119,999 7<br />

$120,000 – $129,999 6<br />

$130,000 – $139,999 6<br />

$140,000 – $149,999 1<br />

$170,000 – $179,999 3<br />

$180,000 – $189,999 3<br />

$200,000 – $209,999 3<br />

$370,000 – $379,999* 1<br />

*Chief Executive Officer<br />

Events subsequent to balance date<br />

The directors are not aware of any matter or circumstance since the end of the financial year that has significantly<br />

affected, or may significantly affect, the operation of the Institute.<br />

Dr Susan Macken Elizabeth Hickey Dr Fiona Thomson-Carter<br />

Chair Director Chief Executive Officer<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 41


Independent auditor’s report<br />

To the readers of the Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited’s financial statements for the year<br />

ended 30 June <strong>2011</strong>.<br />

The Auditor-General is the auditor of the Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited (the<br />

‘Institute’) and the Group, comprising the Institute and its dormant subsidiaries. The Auditor-General has<br />

appointed me, Chris Barber, using the staff and resources of PricewaterhouseCoopers, to carry out an audit of the<br />

financial statements of the Institute and Group on her behalf.<br />

We have audited the financial statements of the Institute and Group on pages 44 to 67, that comprise the<br />

statement of financial position as at 30 June <strong>2011</strong>, the statement of comprehensive income, statement of changes<br />

in equity and statement of cash flows for the year ended on that date; and a summary of significant accounting<br />

policies and other explanatory information.<br />

Opinion on the Financial Statements<br />

In our opinion, the financial statements of the Institute and Group on pages 44 to 67:<br />

• comply with generally accepted accounting practice in New Zealand; and<br />

• comply with International Financial <strong>Report</strong>ing Standards; and<br />

• give a true and fair view of the Institute and Group’s:<br />

– financial position as at 30 June <strong>2011</strong>; and<br />

– financial performance and cash flows for the year ended on that date.<br />

Opinion on other legal requirements<br />

In accordance with the Financial <strong>Report</strong>ing Act 1993 we report that, in our opinion, proper accounting records<br />

have been kept by the Institute and Group as far as appears from an examination of those records.<br />

Our audit was completed on 26 August <strong>2011</strong>, and is the date at which our opinion is expressed.<br />

The basis of our opinion is explained below. In addition, we outline the responsibilities of the Board of Directors<br />

and our responsibilities, and we explain our independence.<br />

Basis of opinion<br />

We carried out our audit in accordance with the Auditor-General’s Auditing Standards, which incorporate<br />

the International Standards on Auditing (New Zealand). Those standards require that we comply with ethical<br />

requirements and plan and carry out our audit to obtain reasonable assurance about whether the financial<br />

statements are free from material misstatement.<br />

Material misstatements are differences or omissions of amounts and disclosures that would affect a reader’s overall<br />

understanding of the financial statements. If we had found material misstatements that were not corrected, we<br />

would have referred to them in our opinion.<br />

An audit involves carrying out procedures to obtain audit evidence about the amounts and disclosures in the<br />

financial statements. The procedures selected depend on our judgement, including our assessment of risks of<br />

material misstatement of the financial statements, whether due to fraud or error. In making those risk assessments<br />

we consider internal control relevant to the entity’s preparation of the financial statements that give a true and<br />

fair view of the matters to which they relate. We consider internal control in order to design audit procedures that<br />

are appropriate in the circumstances but not for the purpose of expressing an opinion on the effectiveness of the<br />

entity’s internal control.<br />

An audit also involves evaluating:<br />

• the appropriateness of accounting policies used and whether they have been consistently applied;<br />

• the reasonableness of the significant accounting estimates and judgements made by the Board<br />

of Directors;<br />

42 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong><br />

• the adequacy of all disclosures in the financial statements; and<br />

• the overall presentation of the financial statements.


We did not examine every transaction, nor do we guarantee complete accuracy of the financial statements. In<br />

accordance with the Financial <strong>Report</strong>ing Act 1993 we report that we have obtained all the information and<br />

explanations we have required. We believe we have obtained sufficient and appropriate audit evidence to provide a<br />

basis for our audit opinion.<br />

Responsibilities of the Board of Directors<br />

The Board of Directors is responsible for preparing financial statements that:<br />

• comply with generally accepted accounting practice in New Zealand;<br />

• give a true and fair view of the Institute and Group’s financial position, financial performance and<br />

cash flows.<br />

The Board of Directors is also responsible for such internal control as it determines is necessary to enable the<br />

preparation of financial statements that are free from material misstatement, whether due to fraud or error.<br />

The Board of Directors’ responsibilities arise from the Financial <strong>Report</strong>ing Act 1993 and the Crown <strong>Research</strong><br />

Institutes Act 1992.<br />

Responsibilities of the Auditor<br />

We are responsible for expressing an independent opinion on the financial statements and reporting that opinion<br />

to you based on our audit. Our responsibility arises from section 15 of the Public Audit Act 2001 and the Crown<br />

<strong>Research</strong> Institutes Act 1992.<br />

Independence<br />

When carrying out the audit, we followed the independence requirements of the Auditor-General, which<br />

incorporate the independence requirements of the New Zealand Institute of Chartered Accountants.<br />

In addition to the audit, we have carried out assignments in the areas of taxation compliance and accounting<br />

advice, which are compatible with those independence requirements. Other than the audit and these assignments,<br />

we have no relationship with, or interests in, the Institute or any of its subsidiaries.<br />

Chris Barber<br />

On behalf of the Auditor-General<br />

Wellington, New Zealand<br />

PricewaterhouseCoopers<br />

Matters relating to the electronic presentation of the audited financial statements<br />

This audit report relates to the financial statements of the Company for the year ended 30 June <strong>2011</strong> included on<br />

the Company’s website. The Company’s Board of Directors is responsible for the maintenance and integrity of the<br />

Company’s website. We have not been engaged to report on the integrity of the Company’s website. We accept<br />

no responsibility for any changes that may have occurred to the financial statements since they were initially<br />

presented on the website.<br />

The audit report refers only to the financial statements named above. It does not provide an opinion on any other<br />

information which may have been hyperlinked to or from the financial statements. If readers of this report are<br />

concerned with the inherent risks arising from electronic data communication they should refer to the published<br />

hard copy of the audited financial statements and the related audit report dated 26 August <strong>2011</strong> to confirm the<br />

information included in the audited financial statements presented on this website. Legislation in New Zealand<br />

governing the preparation and dissemination of financial information may differ from legislation in other<br />

jurisdictions.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 43


Statement of Comprehensive Income<br />

For the year ended 30 June <strong>2011</strong><br />

Group actual Group budget Group actual<br />

year ended year ended year ended<br />

30 June <strong>2011</strong> 30 June <strong>2011</strong> 30 June 2010<br />

audited unaudited audited<br />

Note $’000s $’000s $’000s<br />

Operating revenue<br />

Revenue from rendering of services 51,440 53,476 53,470<br />

51,440 53,476 53,470<br />

Operating expenses<br />

Scientific materials and consumables used (7,388) (7,312) (6,914)<br />

Employee benefit expense (26,587) (27,416) (28,223)<br />

Depreciation and amortisation expense 5/6 (4,539) (5,459) (4,796)<br />

Other expenses 2 (9,309) (9,421) (9,282)<br />

(47,823) (49,608) (49,215)<br />

Operating profit 3,617 3,868 4,255<br />

Finance income – interest income 339 101 265<br />

Finance expense 3 (28) (24) (19)<br />

Net finance income 311 77 246<br />

Profit before income tax expense 3,928 3,945 4,501<br />

Income tax expense 4 (1,285) (1,183) (1,270)<br />

Income tax benefit / (expense) due to change in tax legislation 4 579 – (3,749)<br />

Profit / (loss) for the year attributable to the Institute’s owners 3,222 2,762 (518)<br />

Other comprehensive income – – –<br />

Total comprehensive income / (expense) for the year<br />

attributable to the Institute’s owners 3,222 2,762 (518)<br />

The accompanying notes form an integral part of these financial statements.<br />

44 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Statement of Changes in Equity<br />

For the year ended 30 June <strong>2011</strong><br />

Group actual Group actual Group actual<br />

audited audited audited<br />

share retained<br />

capital earnings total<br />

Note $’000s $’000s $’000s<br />

Balance at 1 July 2009 8,494 24,282 32,776<br />

Loss for the year – (518) (518)<br />

Other comprehensive income – – –<br />

Total comprehensive expense – (518) (518)<br />

Transactions with owners:<br />

Dividend 17 – – –<br />

Balance at 30 June 2010 8,494 23,764 32,258<br />

Profit for the year – 3,222 3,222<br />

Other comprehensive income – – –<br />

Total comprehensive income – 3,222 3,222<br />

Transactions with owners:<br />

Dividend 17 – – –<br />

Balance at 30 June <strong>2011</strong> 8,494 26,986 35,480<br />

The accompanying notes form an integral part of these financial statements.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 45


Statement of Financial Position<br />

As at 30 June <strong>2011</strong><br />

Group actual Group budget Group actual<br />

30 June <strong>2011</strong> 30 June <strong>2011</strong> 30 June 2010<br />

audited unaudited audited<br />

Note $’000s $’000s $’000s<br />

Non-current assets<br />

Property, plant and equipment 5 30,207 37,233 30,499<br />

Intangible assets 6 4,375 – 2,171<br />

34,582 37,233 32,670<br />

Current assets<br />

Cash and cash equivalents 8 7,501 4,158 6,938<br />

Trade and other receivables 9 10,381 6,263 11,497<br />

Current tax receivable 10 249 – –<br />

Inventories 11 1,001 945 1,051<br />

19,132 11,366 19,486<br />

Current liabilities<br />

Trade and other payables 12 10,758 7,246 11,566<br />

Employee benefits 13 2,343 1,805 2,215<br />

Finance lease liabilities 14 164 – 190<br />

Provisions 15 – – 453<br />

Current tax payable 10 – 312 150<br />

13,265 9,363 14,574<br />

Net current assets / (liabilities) 5,867 2,003 4,912<br />

Non-current liabilities<br />

Employee benefits 13 800 1,275 702<br />

Provisions 15 – – 95<br />

Finance lease liabilities 14 129 – 106<br />

Deferred taxation 7 4,040 – 4,421<br />

4,969 1,275 5,324<br />

Net assets 35,480 37,961 32,258<br />

Equity<br />

Share capital 17 8,494 8,494 8,494<br />

Retained earnings 17 26,986 29,467 23,764<br />

Total equity 35,480 37,961 32,258<br />

The Board of Directors of the Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited authorised these financial statements<br />

for issue on 26 August <strong>2011</strong>.<br />

On behalf of the Board:<br />

Dr Susan Macken<br />

Chair<br />

Elizabeth Hickey<br />

Director<br />

Dated 26 August <strong>2011</strong><br />

The accompanying notes form an integral part of these financial statements.<br />

46 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Statement of Cash Flows<br />

For the year ended 30 June <strong>2011</strong><br />

Group actual Group budget Group actual<br />

year ended year ended year ended<br />

30 June <strong>2011</strong> 30 June <strong>2011</strong> 30 June 2010<br />

audited unaudited audited<br />

Note $’000s $’000s $’000s<br />

Cash flows from / (used in) operating activities<br />

Cash was provided from:<br />

Clients 51,897 53,417 52,340<br />

Interest received 312 101 265<br />

52,209 53,518 52,605<br />

Cash was applied to:<br />

Suppliers and employees (43,436) (44,944) (43,314)<br />

Interest paid (28) (24) (19)<br />

Income tax paid 10 (1,485) (1,145) (1,076)<br />

(44,949) (46,113) (44,409)<br />

Net cash inflow from operating activities 18 7,260 7,405 8,196<br />

Cash flows from / (used in) investing activities<br />

Cash was applied to:<br />

Purchase of property, plant and equipment (3,505) (8,737) (3,598)<br />

Purchase of intangible assets (2,989) – (678)<br />

(6,494) (8,737) (4,276)<br />

Net cash outflow from investing activities (6,494) (8,737) (4,276)<br />

Cash flows from / (used in) financing activities<br />

Cash was provided from / (applied to):<br />

Dividends paid – – (106)<br />

Finance lease payments (203) – (231)<br />

Net cash (outflow) / inflow from financing activities (203) – (337)<br />

Net increase / (decrease) in cash held 563 (1,332) 3,583<br />

Cash and cash equivalents at the beginning of the period 6,938 5,490 3,355<br />

Cash and cash equivalents at the end of the period 7,501 4,158 6,938<br />

The accompanying notes form an integral part of these financial statements.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 47


48 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong><br />

Notes to the financial statements<br />

1. Statement of Significant Accounting Policies<br />

a) <strong>Report</strong>ing entity<br />

The financial statements of the Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited (‘ESR’) have been<br />

prepared in accordance with the requirements of the Crown Entities Act 2004, the Crown <strong>Research</strong> Institutes Act<br />

1992, the Companies Act 1993 and the Financial <strong>Report</strong>ing Act 1993.<br />

ESR provides specialist scientific solutions, including working with the New Zealand justice and health sectors to<br />

promote the protection of people and their environment.<br />

ESR is a Crown Entity incorporated and domiciled in New Zealand. The address of its registered office is 34<br />

Kenepuru Drive, Porirua 5240.<br />

The reporting period for these financial statements is the year ended 30 June <strong>2011</strong>.<br />

b) Basis of preparation<br />

The financial statements are prepared on the basis of historical cost. These policies have been consistently applied<br />

to all the periods presented, unless otherwise stated.<br />

The financial statements are Parent and Group financial statements. The two subsidiaries of ESR are dormant<br />

non-trading entities; consequently there is no difference between the financial statements of the Group and those<br />

of the Parent.<br />

c) Statement of compliance<br />

These financial statements have been prepared in accordance with New Zealand Generally Accepted Accounting<br />

Practice (NZ GAAP). They comply with New Zealand equivalents to the International Financial <strong>Report</strong>ing<br />

Standards (NZ IFRS) and other applicable financial reporting standards, as appropriate for profit-oriented<br />

entities. These consolidated financial statements comply with International Financial <strong>Report</strong>ing Standards.<br />

d) Adoption status of relevant new financial reporting standards and<br />

interpretations<br />

1. New and amended standards adopted by the Group<br />

No new standards relevant to the Group’s operations were adopted during the financial year.<br />

2. Standards, amendments and interpretations to existing standards that are not yet effective and<br />

have not been early adopted by the Group<br />

The following standards and amendments to existing standards have been published and are mandatory for<br />

accounting periods beginning on or after 1 January <strong>2011</strong> or later periods, but the Group has not early adopted<br />

them:<br />

NZ IFRS 9, “Financial instruments”, issued in November 2010 (effective for periods beginning on or after 1<br />

January 2013, with early adoption allowed). NZ IFRS 9 replaces the multiple classification and measurement<br />

models in IAS 39 Financial instruments: Recognition and measurement with a single model that has only two<br />

classification categories: amortised cost and fair value. Classification of debt assets is driven by the entity’s business<br />

model for managing the financial assets and the contractual characteristics of the financial assets. All other<br />

financial assets, including investments in complex debt instruments and equity investments, must be recognised<br />

at fair value. All fair value movements must be taken to the income statement, except for equity investments that<br />

are not traded, which may be recorded in the income statement or in reserves. In addition recent additions to<br />

NZ IFRS 9 will simplify the designation and effectiveness testing requirements for financial instruments within<br />

hedging relationships. The Group has not determined when it will adopt NZ IFRS 9 and it is not expected to<br />

have a material impact on the Group’s financial statements.<br />

NZ IAS 24, “Related Party Disclosures”, issued in November 2009 (effective for periods beginning on or after<br />

1 January <strong>2011</strong>, with early adoption allowed). NZ IAS 24 simplifies some of the disclosure requirements and<br />

clarifies the definition of a related party and removes the requirements for government-related entities to disclose<br />

details of all transactions with the Government and other government-related entities. It is not expected to have a<br />

material impact on the Group’s financial statements.<br />

FRS 44, “New Zealand Additional Disclosures”, issued in April <strong>2011</strong> (effective for periods beginning on or after<br />

1 July <strong>2011</strong>, with early adoption allowed). FRS 44 sets out New Zealand-specific disclosures for entities that have<br />

adopted NZ IFRSs. The standard supports the objective of harmonising financial reporting standards in Australia<br />

and New Zealand. It is not expected to have a material impact on the Group’s financial statements.<br />

e) Accounting estimates and judgements<br />

The preparation of financial statements in conformity with NZ IFRS requires judgements, estimates and<br />

assumptions that affect the application of policies and reported amounts of assets and liabilities, income and


expenses. The estimates and associated assumptions are based on historical experience and various other factors<br />

that are believed to be reasonable under the circumstances. Actual results may differ from these estimates.<br />

Management’s judgements, which have the most significant effect on amounts recognised in the financial<br />

statements, are found in Revenue, Taxation and Employee benefits.<br />

i) Revenue<br />

The Group uses the stage of completion method in accounting for its fixed price contracts to deliver scientific<br />

services. The use of the percentage of completion method requires the Group to estimate the services performed<br />

to date as a proportion of the total services to be performed. Stages of completion are calculated and reviewed<br />

monthly, and significant variances are investigated to ensure that the percentage of completion estimate is<br />

reasonable and in line with the overall project plan, estimated completion date and prior measurements of<br />

progress.<br />

ii) Taxation<br />

In May 2010 the Government announced a change to the depreciable nature of buildings. Up until the <strong>2011</strong><br />

income tax year depreciation on buildings up to 2% p.a. was eligible as a tax deduction. Post <strong>2011</strong>, buildings<br />

cease to attract tax depreciation. In recognition of the fact that some entities had not fully split fit-out-related<br />

assets from building assets, the IRD agreed that an entity on a building-by-building basis could claim either of the<br />

following as a future tax deduction:<br />

1. 2% of 15% of the NBV of the building commencing from the 2012 income tax year: OR<br />

2. If the entity can split the fit-out element from building and provide support for the appropriateness of the split<br />

they could claim depreciation at the relevant tax rates upon these assets.<br />

ESR has commenced an exercise to identify and separate the fit-out components of buildings from the building<br />

structure. This exercise is in its preliminary stage. Given the early stage of the exercise, ESR has recognised an<br />

adjustment to deferred tax of $579,000 based upon the first option (15% of the NBV of buildings). Management<br />

believes that this provides a more reliable and supportable measure for such an adjustment as at 30 June <strong>2011</strong>.<br />

iii) Employee benefits<br />

In determining the future entitlements of employees, management is required to make judgements on anticipated<br />

length of service, future salary levels and discount rates. Reference is made to historical data in determining<br />

appropriate factors to apply.<br />

Key assumptions:<br />

• Anticipated length of service: Management opinion is that current length of service and staff turnover rate<br />

provide an accurate basis for determining future length of service<br />

• Future salary levels: Management consider the rate of inflation and the current employment market over a<br />

three to five-year horizon in arriving at a suitable rate for wage increases<br />

• Discount rates: Management uses the five-year Government Bond interest rate as a discount factor, currently<br />

3.99% (2010: 4.85%).<br />

The pre-tax impact on the Statement of Comprehensive Income of fluctuations in the above assumptions is<br />

detailed in the table below:<br />

Discount rate Future salary level Attrition rate<br />

-1% +1% -1% +1% -1% +1%<br />

$000’s $000’s $000’s $000’s $000’s $000’s<br />

Personal development leave 120 (97) (7) 7 15 (15)<br />

Retirement leave 4 (4) (4) 4 0 0<br />

124 (101) (11) 11 15 (15)<br />

Parentheses indicate an increase in ESR’s profit.<br />

f) Principles of consolidation<br />

Subsidiaries<br />

The consolidated financial statements incorporate the assets and liabilities of all subsidiaries of ESR as at 30 June<br />

<strong>2011</strong> and the results of the operations of all subsidiaries for the year then ended. ESR and its subsidiaries together<br />

are referred to in these financial statements as the Group.<br />

Subsidiaries are all those entities over which the Group has the power to govern financial and operating policies,<br />

generally accompanying a shareholding of more than one-half of the voting rights. The existence and effect of<br />

potential voting rights that are currently exercisable or convertible are considered when assessing whether ESR<br />

controls another entity.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 49


Subsidiaries that form part of the Group are consolidated from the date on which control is transferred to ESR.<br />

They are de-consolidated from the date that control ceases.<br />

The acquisition method of accounting is used to account for the acquisition of subsidiaries by the Group. The cost<br />

of an acquisition is measured as the fair value of the assets given, equity instruments issued and liabilities incurred<br />

or assumed at the date of exchange. Identifiable assets acquired and liabilities and contingent liabilities assumed in<br />

a business combination are measured initially at their fair values at the acquisition date, irrespective of the extent<br />

of any non-controlling interest. The excess of the cost over the fair value of the Group’s share of the identifiable<br />

net assets acquired is recorded as goodwill. If the cost of acquisition is less than the Group’s share of the fair value<br />

of the identifiable net assets of the subsidiary acquired, the difference is recognised directly in the Statement of<br />

Comprehensive Income.<br />

Intercompany transactions, balances and unrealised gains on transactions between subsidiary companies are<br />

eliminated. Unrealised losses are also eliminated unless the transaction provides evidence of the impairment of<br />

the asset transferred. Accounting policies of subsidiaries are consistent with those policies adopted by the Group.<br />

g) Property, plant and equipment<br />

Items of property, plant and equipment are initially recorded at cost, and subsequently at cost less accumulated<br />

depreciation and impairment. The cost of property, plant and equipment includes the value of the consideration<br />

given to acquire the assets and the value of other directly attributable costs that have been incurred in bringing the<br />

assets to the locations and condition necessary for their intended use.<br />

The carrying amounts of plant, property and equipment are reviewed at least annually to determine if there is<br />

any indication of impairment. Where an asset’s recoverable amount is less than its carrying amount, it will be<br />

reported at its recoverable amount and an impairment loss will be recognised. Losses resulting from impairment<br />

are reported in the Statement of Comprehensive Income.<br />

Realised gains and losses arising from the disposal of property, plant and equipment are recognised in the<br />

Statement of Comprehensive Income in the periods in which the transactions occur.<br />

Depreciation is charged on a straight-line basis at rates calculated to allocate the cost of an item of property,<br />

plant and equipment, less any estimated residual value, over its estimated useful life. The estimated useful lives of<br />

different classes of property, plant and equipment are as follows:<br />

Freehold buildings<br />

Leasehold improvements<br />

Plant, equipment and vehicles<br />

IT equipment and internal software<br />

20 – 50 years<br />

10 years<br />

3 – 10 years<br />

3 years<br />

h) Intangible assets<br />

i) Computer software<br />

Items of computer software that do not comprise an integral part of the related hardware are treated as intangible<br />

assets with finite lives. Intangible assets with finite lives are recorded at cost, and subsequently recorded at<br />

cost less any accumulated amortisation and impairment losses. Amortisation is charged to the Statement of<br />

Comprehensive Income on a straight-line basis over the useful life of the asset. Typically, the estimated useful life<br />

of computer software is three years.<br />

ii) Development costs – internally generated intangible assets<br />

The cost of an internally generated intangible asset represents expenditure incurred in the development phase<br />

of the asset only. The development phase occurs after the following can be demonstrated: technical feasibility;<br />

ability to complete the asset; intention and ability to sell or use the asset; ability to generate probable future<br />

economic benefits; and development expenditure can be reliably measured. Expenditure incurred on research<br />

of an internally generated intangible asset is expensed when it is incurred. Where the research phase cannot be<br />

distinguished from the development phase, the expenditure is expensed when it is incurred.<br />

i) Impairment of non-financial assets<br />

Assets that are subject to amortisation are reviewed for impairment whenever events or changes in circumstances<br />

indicate that the carrying amount may not be recoverable. An impairment loss is recognised for the amount by<br />

which the asset’s carrying amount exceeds its recoverable amount. The recoverable amount is the higher of an<br />

asset’s fair value less costs to sell and value in use. For the purposes of assessing impairment, assets are grouped at<br />

the lowest levels for which there are separately identifiable cash flows (cash-generating units).<br />

j) Taxation<br />

The income tax expense for the period is the tax payable on the current period’s taxable income based on the<br />

national income tax rate for each jurisdiction. This is then adjusted by changes in deferred tax assets and liabilities<br />

attributable to temporary differences between the tax bases of assets and liabilities and their carrying amounts in<br />

the financial statements, and unused tax losses.<br />

50 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


Deferred tax assets and liabilities are recognised for temporary differences at the tax rates expected to apply<br />

when the assets are recovered or liabilities settle. The relevant tax rates are applied to the cumulative amount of<br />

deductible and taxable temporary differences to measure the deferred tax asset or liability. An exception is made<br />

for certain temporary differences arising from the initial recognition of an asset or a liability. No deferred tax asset<br />

or liability is recognised in relation to temporary differences if they arose in a transaction, other than a business<br />

combination, and at the time of the transaction did not affect either accounting profit or taxable profit or loss.<br />

Deferred tax assets are recognised for deductible temporary differences and unused tax losses only if it is probable<br />

that future taxable amounts will be available to utilise those temporary differences and losses.<br />

Deferred tax liabilities and assets are not recognised for temporary differences between the carrying amount<br />

and the tax bases of investments in controlled entities where the Parent entity is able to control the timing of<br />

the reversal of the temporary differences and it is probable that the differences will not reverse in the foreseeable<br />

future.<br />

Deferred income tax assets are recognised to the extent that it is probable that future taxable profit will be<br />

available against which the temporary differences can be utilised.<br />

k) Cash and cash equivalents<br />

Cash means cash on hand, demand deposits and other highly liquid investments in which ESR has invested as<br />

part of its day-to-day cash management. The following definitions are used in the Statement of Cash Flows:<br />

• Investing activities are those activities relating to the acquisition, holding and disposal of fixed assets and<br />

investments<br />

• Financing activities are those activities that result in changes in the size and composition of the capital<br />

structure of ESR and this includes both equity and debt not falling within the definition of cash. Dividends<br />

paid in relation to the capital structure are included in financing activities<br />

• Operating activities are the principal revenue-producing activities and other activities that are not investing<br />

or financing activities.<br />

l) Trade and other receivables<br />

Trade receivables are stated at their estimated realisable value after providing against debts where collection is<br />

doubtful. An estimate of the value of doubtful debts is made based on a review of debts at year end. Bad debts are<br />

written off in the period in which they are identified.<br />

m) Inventories<br />

Stocks of consumables and work in progress are stated at the lower of cost and net realisable value. Cost is<br />

determined on a first in, first out basis.<br />

n) Trade and other payables<br />

These amounts represent the best estimate of the expenditure required to settle an obligation arising from goods<br />

or services provided to ESR prior to period end. These amounts are unsecured and are usually paid within 30<br />

days of recognition. Liabilities and provisions to be settled beyond 12 months are recorded at their present value.<br />

o) Employee benefits<br />

i) Wages, salaries and annual leave<br />

Liabilities for wages and salaries, including annual leave, that are expected to be settled within 12 months of the<br />

reporting date are recognised in respect of employees’ services up to the reporting date and are measured at the<br />

amounts expected to be paid when the liabilities are settled.<br />

Obligations for contributions to defined contribution retirement plans are recognised in the Statement of<br />

Comprehensive Income as they fall due.<br />

ii) Long service leave, retirement leave and development leave<br />

The liability for long service leave, retirement leave and development leave is recognised as an employee benefit<br />

liability and measured as the present value of expected future payments to be made in respect of services provided<br />

by employees up to the reporting date. Consideration is given to the expected future salary levels, experience of<br />

employee departures and periods of service. Expected future payments are discounted using market yields at the<br />

reporting date for Government Bonds with terms to maturity and currency that match, as closely as possible, the<br />

estimated future cash outflows.<br />

p) Leases<br />

Finance leases transfer to ESR, as lessee, substantially all the risks and rewards incidental to ownership of a leased<br />

asset. Initial recognition of a finance lease results in an asset and liability being recognised at amounts equal to the<br />

lower of the fair value of the leased asset or the present value of the minimum lease payments. Each lease payment<br />

is allocated between the liability and finance charges so as to achieve a constant rate of finance charge over the<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 51


term of the lease. Property, plant and equipment acquired under a finance lease are depreciated over the shorter of<br />

the assets’ useful lives and lease terms.<br />

Leases in which a significant portion of the risks and rewards of ownership are retained by the lessor are classified<br />

as operating leases. Payments made under operating leases (net of any incentives received from the lessor) are<br />

charged to the Statement of Comprehensive Income on a straight-line basis over the period of the lease.<br />

q) Borrowings<br />

Borrowings are initially recognised at fair value, net of costs incurred. Borrowings are subsequently measured<br />

at amortised cost. Any differences between the proceeds (net of transaction costs) and the redemption amount<br />

is recognised in the Statement of Comprehensive Income over the period of the borrowing using the effective<br />

interest method.<br />

Borrowings are classified as current liabilities unless ESR has an unconditional right to defer settlement of the<br />

liability for at least 12 months after the balance date.<br />

r) Share capital<br />

Ordinary shares are classified as equity.<br />

Incremental costs directly attributable to the issue of new shares or options are shown as appropriate in equity as a<br />

deduction, net of tax, from the proceeds.<br />

s) Revenue<br />

i) Sales of goods and services<br />

Revenue is earned by ESR in exchange for the provision of outputs (services) to third parties. Revenue from the<br />

supply of services is measured at the fair value of consideration received. Revenue from the supply of services is<br />

recognised in the accounting period in which the services are rendered, by reference to the stage of completion<br />

of the specific transaction assessed on the basis of the actual service provided as a proportion of the total services<br />

to be provided. Any revenue for which services have not been supplied as at the reporting date but for which<br />

payment has been received is deferred within the Statement of Financial Position as revenue in advance.<br />

ii) Interest income<br />

Interest income is recognised in the Statement of Comprehensive Income on a time proportion basis, using the<br />

effective interest rate method.<br />

iii) Vaccine revenue<br />

ESR purchases vaccines on behalf of the Ministry of Health. The Ministry of Health retains the risks and rewards<br />

related to the inventory and as such no inventory is recognised within ESR’s Statement of Financial Position. ESR<br />

receives and recognises commission revenue only in relation to the services performed.<br />

T) Foreign currency<br />

Items included in the financial statements of each of the Group’s entities are measured using the currency of the<br />

primary economic environment in which the entity operates. The Group financial statements are presented in<br />

New Zealand dollars (NZD), which is ESR’s functional and presentation currency.<br />

Transactions in foreign currencies are initially translated at the foreign exchange rates at the dates of the<br />

transactions. Foreign exchange gains and losses resulting from the settlement of such transactions, and from the<br />

translation at year-end exchange rates of monetary assets and liabilities denominated in foreign currencies, are<br />

recognised in the Statement of Comprehensive Income.<br />

Non-monetary assets and liabilities measured at historical cost in a foreign currency are translated using the<br />

exchange rate at the date of the transaction.<br />

u) Goods and services tax<br />

Items in the Statement of Comprehensive Income and Statement of Cash Flows are disclosed net of Goods and<br />

Services Tax (“GST”). All items in the Statement of Financial Position are stated net of GST with the exception of<br />

receivables and payables, which include GST invoiced.<br />

v) Dividends<br />

A provision is made for the amount of any dividend declared on or before the end of the financial year but not<br />

distributed at balance date.<br />

w) Financial instruments<br />

The designation of financial assets and financial liabilities by ESR into instrument categories is determined by the<br />

business purposes of the financial instruments, policies and practices of management, the relationship with other<br />

instruments and the reporting costs and benefits associated with each designation. The designations applied by<br />

ESR are reflected in the financial statements.<br />

52 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


i) Financial assets<br />

Classification<br />

The Group classifies its financial assets as loans and receivables. Management determines the classification of its<br />

financial assets at initial recognition.<br />

(a) Loans and receivables<br />

Loan and receivables are non-derivative financial assets with fixed or determinable payments that are not quoted<br />

in an active market. They are included in current assets, except for maturities greater than 12 months after the<br />

reporting date. These are classified as non-current assets. ESR’s loans and receivables comprise “trade and other<br />

receivables” and “cash and cash equivalents” in the Statement of Financial Position.<br />

(b) Recognition and measurement<br />

Regular purchases and sales of financial assets are recognised on the trade-date – the date on which the Group<br />

commits to purchase or sell the asset. Investments are initially recognised at fair value plus transaction costs for all<br />

financial assets not carried at fair value through profit or loss. Financial assets are derecognised when the rights<br />

to receive cash flows from the investments have expired or have been transferred and the Group has transferred<br />

substantially all risks and rewards of ownership. Loans and receivables are carried at amortised cost using the<br />

effective interest method.<br />

The Group assesses at each reporting date whether there is objective evidence that a financial asset or a group of<br />

financial assets is impaired.<br />

ii) Financial liabilities<br />

Financial liabilities held by ESR include trade and other payables.<br />

Such financial liabilities are recognised initially at fair value less transaction costs and subsequently measured at<br />

amortised cost using the effective interest rate method. Financial liabilities entered into with durations less than<br />

12 months are recognised at their nominal value.<br />

iii) Derivatives<br />

Derivative financial instruments are recognised both initially and subsequently at fair value. They are reported as<br />

either assets or liabilities depending on whether the derivative is in a net gain or net loss position. ESR does not<br />

use hedge accounting, and as such derivatives are classified as held-for-trading financial instruments with fair value<br />

gains or losses recognised in the Statement of Comprehensive Income. Such derivatives are entered into for risk<br />

management purposes.<br />

x) Provisions<br />

Provisions are recognised when: ESR has a present legal or constructive obligation as a result of past events; it<br />

is probable that an outflow of resources will be required to settle the obligation; and the amount can be reliably<br />

estimated. Restructuring provisions comprise employee termination payments. Provisions are not recognised for<br />

future operating losses.<br />

Provisions are measured at the present value of the expenditures expected to be required to settle each obligation<br />

using a pre-tax rate that reflects current market assessments of the time value of money and the risks specific to<br />

the obligation. The increase in the provision due to the passage of time is recognised as an interest expense.<br />

y) Changes in accounting policies<br />

Accounting policies have been applied on a basis consistent with the prior year.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 53


2. Other expenses include the following specific items:<br />

Group<br />

Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

Note $’000s $’000s<br />

Fees paid to PricewaterhouseCoopers for:<br />

– the audit of the statutory financial statements 83 77<br />

Total audit-related fees paid to the auditor 83 77<br />

– non-audit-related services – taxation compliance 35 30<br />

– non-audit-related services – accounting advice – 5<br />

Total fees paid to auditor 118 112<br />

Defined contribution plan expense 197 181<br />

Directors’ fees 21 190 190<br />

Donations 4 11<br />

Bad debts written off 21 2<br />

Communications 1,496 1,723<br />

Consultancy fees 1,176 1,090<br />

Impairment of development costs – 40<br />

Foreign exchange loss 15 5<br />

Loss on sale of fixed assets 10 8<br />

Marketing and advertising 150 189<br />

Office and administration 1,139 1,157<br />

Occupancy 1,933 2,056<br />

Rental and operating lease costs 439 410<br />

Training and conferences 309 303<br />

Travel 1,347 1,180<br />

Restructuring expense – 693<br />

Business acquisition costs 262 –<br />

Given the nature of ESR’s principal business activities, research comprises part of ESR’s everyday business<br />

operations. As such, expenses relating to research are not separately identified. The cost of research to ESR<br />

is distributed between the relevant expense items, for example employee benefits and scientific materials<br />

used.<br />

Fees paid to the auditor for taxation compliance include work in relation to the review of ESR's annual tax return<br />

and other sundry taxation advice.<br />

During the year ESR incurred costs of $262,000 related to the potential acquisition of a business unit of a<br />

Government Ministry. The costs principally relate to financial and legal due diligence. It is expected that the<br />

acquisition will be completed in the June 2012 financial year.<br />

3. Finance expense<br />

Group<br />

Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s<br />

$’000s<br />

Finance lease interest 28 19<br />

28 19<br />

54 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


4. Taxation<br />

The taxation charge has been calculated as follows:<br />

Group<br />

Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

Note $’000s $’000s<br />

Profit before income tax expense 3,928 4,501<br />

Prima facie taxation at 30% 1,178 1,350<br />

Plus taxation effect of:<br />

Net prior year under / (over) estimation 21 (109)<br />

Impact of change in tax legislation – building depreciation (579) 4,133<br />

Impact of change in corporate income tax rate 25 (384)<br />

Non-deductible / (assessable) items 61 29<br />

Tax expense for the year 706 5,019<br />

The tax expense for the year is represented by:<br />

Current taxation 1,087 956<br />

Deferred taxation 7 (381) 4,063<br />

As a result of the change in tax legislation that was enacted on 27 May 2010, with effect from 1 July <strong>2011</strong> being<br />

the beginning of the 2012 income year, the tax depreciation rate on buildings with estimated useful lives of 50<br />

years or more will be reduced to 0%. This reduction in the tax depreciation rate has significantly reduced the tax<br />

base of ESR's buildings, as future tax deductions will no longer be available from the <strong>2011</strong>-2012 income year.<br />

This has resulted in an increase to the deferred tax liability in relation to buildings by $4,133,000, which was<br />

recognised in the tax expense in the previous year.<br />

As a result of these changes, ESR has commenced a project to assess the division of its buildings between<br />

depreciable and non-depreciable components for tax purposes. As at 30 June <strong>2011</strong> ESR had made an initial<br />

assessment that 15% of buildings were depreciable. This is in line with the guidance provided by Inland<br />

Revenue. As a result a credit of $579,000 has been recognised in tax expense in the year ended 30 June <strong>2011</strong>.<br />

Further work will be completed in the coming year to confirm the position. It is likely this will result in an<br />

additional adjustment.<br />

As a result of the change in the New Zealand corporate tax rate from 30% to 28% that was enacted on 27<br />

May 2010 and that will be effective from 1 July <strong>2011</strong>, the relevant deferred tax balances have been remeasured.<br />

Deferred tax expected to reverse in the year to 30 June 2012 or later has been measured using the effective rate<br />

that will apply for the period (28%).<br />

706 5,019<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 55


5. Property, plant and equipment<br />

Group<br />

Buildings<br />

and IT Plant, Assets<br />

Freehold leasehold equipment equipment under<br />

land improvements and software and vehicles construction Total<br />

$’000s $’000s $’000s $’000s $’000s $’000s<br />

At 1 July 2009<br />

Cost 476 22,798 10,596 22,675 814 57,359<br />

Accumulated depreciation – (3,649) (8,838) (14,088) – (26,575)<br />

Net book value at the beginning of the year 476 19,149 1,758 8,587 814 30,784<br />

Year ended 30 June 2010<br />

Net book value at the beginning of the year 476 19,149 1,758 8,587 814 30,784<br />

Additions – 184 745 1,541 941 3,411<br />

Transfers:<br />

– From assets under construction – 23 248 538 (809) –<br />

Disposals – – (10) (12) – (22)<br />

Depreciation for the year – (465) (1,136) (2,073) – (3,674)<br />

Net book value at the end of the year 476 18,891 1,605 8,581 946 30,499<br />

At 30 June 2010<br />

Cost 476 23,006 9,752 23,897 946 58,077<br />

Accumulated depreciation – (4,115) (8,147) (15,316) – (27,578)<br />

Net book value at the end of the year 476 18,891 1,605 8,581 946 30,499<br />

Year ended 30 June <strong>2011</strong><br />

Net book value at the beginning of the year 476 18,891 1,605 8,581 946 30,499<br />

Additions – 718 608 1,912 267 3,505<br />

Transfers from assets under construction – 652 39 250 (941) –<br />

Disposals – (7) – (4) – (11)<br />

Depreciation for the year – (495) (1,019) (2,272) – (3,786)<br />

Net book value at the end of the year 476 19,759 1,233 8,467 272 30,207<br />

At 30 June <strong>2011</strong><br />

Cost 476 24,367 8,519 25,948 272 59,582<br />

Accumulated depreciation – (4,608) (7,286) (17,481) – (29,375)<br />

Net book value at the end of the year 476 19,759 1,233 8,467 272 30,207<br />

IT equipment recognised under finance leases (where ESR is a lessee) included in the above table, has the<br />

following values.<br />

Group<br />

30 June 30 June<br />

<strong>2011</strong> 2010<br />

$’000s $’000s<br />

Cost – capitalised finance lease assets 686 631<br />

Accumulated depreciation (520) (331)<br />

Net book value at the end of the year 166 300<br />

ESR does not have any property, plant and equipment where title is restricted or used as security for liabilities.<br />

56 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


6. Intangible assets<br />

Group<br />

Computer Computer<br />

software – software – Assets<br />

externally internally Development under<br />

purchased generated costs construction Total<br />

$’000s $’000s $’000s $’000s $’000s<br />

At 1 July 2009<br />

Cost 2,664 1,253 308 470 4,695<br />

Accumulated amortisation (1,393) (804) (268) – (2,465)<br />

Net book value at the end of the year 1,271 449 40 470 2,230<br />

Year ended 30 June 2010<br />

Net book value at the beginning of the year 1,271 449 40 470 2,230<br />

Additions 158 89 – 856 1,103<br />

Transfers from assets under construction 212 257 – (469) –<br />

Impairment losses – – (40) – (40)<br />

Amortisation for the year (677) (445) – – (1,122)<br />

Net book value at the end of the year 964 350 – 857 2,171<br />

At 30 June 2010<br />

Cost 3,113 1,599 308 857 5,877<br />

Accumulated amortisation and impairment losses (2,149) (1,249) (308) – (3,706)<br />

Net book value at the end of the year 964 350 – 857 2,171<br />

Year ended 30 June <strong>2011</strong><br />

Net book value at the beginning of the year 964 350 – 857 2,171<br />

Additions 103 – – 2,854 2,957<br />

Transfers from assets under construction – – – – –<br />

Impairment losses – – – – –<br />

Amortisation for the year (589) (164) – – (753)<br />

Net book value at the end of the year 478 186 – 3,711 4,375<br />

At 30 June <strong>2011</strong><br />

Cost 2,224 2,183 – 3,711 8,118<br />

Accumulated amortisation and impairment losses (1,746) (1,997) – – (3,743)<br />

Net book value at the end of the year 478 186 – 3,711 4,375<br />

ESR does not have any intangible assets whose title is restricted or used as security for liabilities.<br />

Assets under construction relates to the development of a new operational system. This is expected to be fully<br />

implemented within the <strong>2011</strong>-2012 financial year.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 57


7. Deferred taxation<br />

Deferred tax assets and liabilities are attributed to the following:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Balance at the beginning of the year (4,421) (358)<br />

Statement of Comprehensive Income charge 381 (4,063)<br />

Balance at the end of the year (4,040) (4,421)<br />

Employee<br />

Accelerated tax benefits and<br />

depreciation provisions Total<br />

$’000s $’000s $’000s<br />

Year ended 30 June 2010<br />

Balance at the beginning of the year (1,311) 953 (358)<br />

Change in corporate income tax rate 397 (13) 384<br />

Charged / (credited) to Statement of Comprehensive Income (4,370) (77) (4,447)<br />

Balance at the end of the year (5,284) 863 (4,421)<br />

Year ended 30 June <strong>2011</strong><br />

Balance at the beginning of the year (5,284) 863 (4,421)<br />

(Under) / over provision in prior year (4) 214 210<br />

Deferred tax liability adjustment – (25) (25)<br />

Impact of change in tax legislation – building depreciation 579 – 579<br />

Charged / (credited) to Statement of Comprehensive Income (189) (194) (383)<br />

Balance at the end of the year (4,898) 858 (4,040)<br />

There are no unrecognised deferred tax assets or liabilities.<br />

Deferred tax liabilities expected to be settled within 12 months total $367,000 (2010: $394,000).<br />

8. Cash and cash equivalents<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Cash at bank and on hand 128 2<br />

Short-term deposits 7,373 6,936<br />

7,501 6,938<br />

58 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


9. Trade and other receivables<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Trade debtors 9,640 10,880<br />

Provision for doubtful debts (20) (29)<br />

9,620 10,851<br />

Prepayments 761 646<br />

Movements on ESR’s provision for impairment of trade receivables are as follows:<br />

10,381 11,497<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

As at 1 July 29 31<br />

Provision for doubtful debts 12 –<br />

Receivables written off during the year as uncollectable (21) (2)<br />

As at 30 June <strong>2011</strong>, trade receivables of $20,000 (2010: $29,000) were impaired and provided for. The<br />

individually impaired receivables mainly relate to customers, which are in unexpectedly difficult economic<br />

situations. The ageing of these receivables is as follows:<br />

20 29<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Past due 1 – 30 days – 11<br />

Past due 31 – 60 days – 9<br />

Past due > 61 days 20 9<br />

20 29<br />

As at 30 June <strong>2011</strong>, trade receivables of $211,000 (2010: $242,000) were past due but not impaired. These<br />

relate to a number of customers for which there is no recent history of default. The ageing analysis of these trade<br />

receivables is as follows:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Past due 1 – 30 days 57 78<br />

Past due 31 – 60 days 33 154<br />

Past due > 61 days 121 10<br />

211 242<br />

10. Income tax receivable / (payable)<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Balance at the beginning of the year (150) (229)<br />

Current year charge (1,083) (956)<br />

Prior period adjustment (3) (41)<br />

Provisional taxation payments 1,485 1,076<br />

Balance at the end of the year 249 (150)<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 59


11. Inventories<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Scientific materials and consumables 1,001 1,051<br />

1,001 1,051<br />

12. Trade and other payables<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Accrued expenses 468 839<br />

Payroll and GST accruals 1,064 1,072<br />

Revenue in advance 1,234 1,052<br />

Trade payables 7,992 8,603<br />

10,758 11,566<br />

13. Employee benefits<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

<strong>Annual</strong> leave accrual 2,048 1,871<br />

Personal development leave accrual 255 225<br />

Retirement leave accrual – 66<br />

Other 40 53<br />

Current liabilities 2,343 2,215<br />

Personal development leave accrual 690 598<br />

Retirement leave accrual 104 98<br />

Other 6 6<br />

Non-current liabilities 800 702<br />

14. Finance lease liabilities<br />

Future minimum lease payments are as follows:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Not later than one year 178 199<br />

Later than one year and not later than five years 137 117<br />

Later than five years – –<br />

Total minimum lease payments 315 316<br />

Future finance charges on finance leases (22) (20)<br />

Present value of finance lease liabilities 293 296<br />

The finance leases relate to IT equipment. Upon termination of the initial lease period, ESR can choose to<br />

either extend the term further, or return the leased assets to the lessor. There is no option to purchase the leased<br />

assets upon termination of the lease.<br />

The present values of finance lease liabilities are as follows:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Not later than one year 164 190<br />

Later than one year and not later than five years 129 106<br />

Later than five years – –<br />

293 296<br />

60 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


15. Provisions<br />

Warranty<br />

ESR is no longer obligated to provide technical assistance for a forensic system supplied to an international<br />

client and to rectify subsystems that do not perform satisfactorily. The provision was released in the current year<br />

(2010: $190,000).<br />

Restructuring<br />

No restructuring activities took place in the current year (2010: Due to the significant decline in the<br />

Pharmaceutical business and loss of some Health Service Descriptions, ESR has restructured a small portion of<br />

the business. The full cost associated with the restructuring was recognised in the previous period).<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Restructuring – current portion – 358<br />

Warranty – current portion – 95<br />

– 453<br />

Warranty – non current portion – 95<br />

Total provisions – 548<br />

Movements in each class of provisions are as follows:<br />

Warranty Restructuring Total<br />

$’000s $’000s $’000s<br />

As at 1 July 2010 190 358 548<br />

Utilisation – (358) (358)<br />

Additions – – –<br />

Release of provision to Statement of Comprehensive Income (190) – (190)<br />

Closing balance as at 30 June <strong>2011</strong> – – –<br />

16. Borrowings<br />

ESR holds a multi-option credit facility with Westpac Banking Corporation for $6,000,000 (2010:<br />

$6,000,000), which is provided subject to ESR meeting an equity ratio covenant specified by the bank. The<br />

facility expires in March 2014, and as at 30 June <strong>2011</strong> no borrowings have been entered into under this facility<br />

(30 June 2010: Nil).<br />

There were no breaches of the equity ratio covenant during the year.<br />

17. Equity<br />

Share capital<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

8,494,000 ordinary shares (issued and fully paid) 8,494 8,494<br />

All ordinary shares rank equally with one vote attached to each fully paid ordinary share. Ordinary shares have<br />

no par value.<br />

No dividends were proposed or declared for the 30 June <strong>2011</strong> year (2010: Nil).<br />

Retained earnings<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Balance at the beginning of the year 23,764 24,282<br />

Dividend paid – –<br />

Profit / (loss) for the year 3,222 (518)<br />

Balance at the end of the year 26,986 23,764<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 61


18. Reconciliation of profit / (loss) after taxation to cash flows from<br />

operating activities<br />

Group Group<br />

year ended year ended<br />

30 June <strong>2011</strong> 30 June 2010<br />

Note $’000s $’000s<br />

Profit / (loss) for the year after taxation 3,222 (518)<br />

Non-cash items:<br />

Depreciation and amortisation 4,539 4,796<br />

Finance charges on leases 203 –<br />

Impairment of investment – 40<br />

Bad debts written off 2 21 2<br />

(Decrease) / increase in deferred taxation liability 4 (381) 4,063<br />

Foreign exchange loss 12 5<br />

4,394 8,906<br />

Impact of changes in investing activities:<br />

Loss / (gain) on sale of assets 10 8<br />

10 8<br />

Financing<br />

Dividend payable – 106<br />

– 106<br />

Changes in working capital:<br />

Decrease / (increase) in trade and other receivables 1,116 (590)<br />

(Decrease) / increase in income tax payable (399) (79)<br />

Decrease / (increase) in inventories 50 (231)<br />

(Decrease) / increase in provisions (548) 154<br />

Increase / (decrease) in employment benefits 226 (41)<br />

(Decrease) / increase in financial liabilities (3) 4<br />

(Decrease) / increase in trade and other payables (808) 477<br />

(366) (306)<br />

Net cash inflow / (outflow) from operating activities 7,260 8,196<br />

19. Investments<br />

Subsidiary companies<br />

ESR has two wholly owned, non-trading, subsidiary companies:<br />

Country<br />

Balance<br />

of<br />

Name date incorporation<br />

ESR Limited 30 June New Zealand<br />

The Institute of <strong>Environmental</strong> <strong>Science</strong> and <strong>Research</strong> Limited 30 June Australia<br />

All subsidiaries have remained non-trading during the period. ESR Holdings Sdn Bhd was deregistered in the<br />

2010 year.<br />

At balance date the investment in these subsidiaries had a nil carrying value.<br />

62 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


20. Commitments<br />

Capital commitments<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Property, plant and equipment 212 759<br />

Total capital commitments 212 759<br />

Operating lease commitments<br />

The future aggregate minimum lease payments under non-cancellable operating leases are as follows:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Not later than one year 333 311<br />

Later than one year and not later than five years 1,200 1,118<br />

Later than five years – 277<br />

Total operating commitments 1,533 1,706<br />

ESR leases land, a building, equipment and vehicles. There is a renewal option in respect of the land and<br />

building lease. There are no renewal options or options to purchase in respect of vehicles held under operating<br />

leases.<br />

ESR has a number of standard operational agreements for the purchase of materials and consumables that have<br />

both fixed and variable components, some of which extend beyond one year.<br />

21. Related party transactions and key management personnel<br />

Related party transactions<br />

ESR is a wholly owned entity of the Crown. ESR enters into transactions with other Crown entities and<br />

government departments.<br />

Related parties include the subsidiary entities disclosed in note 19. There were no transactions with these related<br />

parties in the year ended 30 June <strong>2011</strong> (30 June 2010: Nil).<br />

The following transactions were carried out with related parties:<br />

• There are close family members of key management personnel employed by ESR. The terms and conditions<br />

of those arrangements are no more favourable than those ESR would have adopted if there were no<br />

relationships with key management personnel<br />

• Fees paid to directors during the year were $190,000 (30 June 2010: $190,000), with no balances outstanding<br />

at balance date (30 June 2010: Nil).<br />

No provision was required, nor any expense recognised, for impairment of receivables from related parties.<br />

Key management personnel compensation<br />

Key management personnel comprise the Chief Executive Officer, members of the Strategic Leadership Team<br />

and the Directors. Key management personnel compensation is disclosed below.<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Salaries and other short-term employee benefits 1,840 1,873<br />

Other long-term employee benefits 78 83<br />

Directors’ fees 190 190<br />

Total key management personnel compensation 2,108 2,146<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 63


22. Financial instruments by category<br />

Loans and<br />

receivables<br />

$’000s<br />

30 June 2010<br />

Assets as per balance sheet<br />

Trade and other receivables excluding prepayments 10,851<br />

Cash and cash equivalents 6,938<br />

Total 17,789<br />

Financial<br />

liabilities at<br />

amortised cost<br />

$’000s<br />

Liabilities as per balance sheet<br />

Finance lease liabilities 296<br />

Trade and other payables 9,442<br />

Total 9,738<br />

Loans and<br />

receivables<br />

$’000s<br />

30 June <strong>2011</strong><br />

Assets as per balance sheet<br />

Trade and other receivables excluding prepayments 9,620<br />

Cash and cash equivalents 7,501<br />

Total 17,121<br />

Financial<br />

liabilities at<br />

amortised cost<br />

$’000s<br />

Liabilities as per balance sheet<br />

Finance lease liabilities 293<br />

Trade and other payables 8,460<br />

Total 8,753<br />

64 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


23. Financial risk management<br />

ESR’s activities are exposed to a variety of financial risks: market risk, credit risk, liquidity risk, cash flow risk<br />

and fair value interest-rate risk. ESR’s overall risk management programme focuses on the unpredictability of<br />

financial markets and seeks to minimise potential adverse effects on ESR’s financial performance. The policies<br />

approved and financial instruments being utilised at balance date are outlined below.<br />

a) Market risk<br />

In accordance with its Treasury Management Policy, ESR uses derivative financial instruments to economically<br />

hedge its exposure to foreign exchange risks from its operational, financing and investment activities. These<br />

derivatives are classified at fair value through profit or loss, and gains and losses are recognised in the Statement<br />

of Comprehensive Income.<br />

i) Foreign exchange risk<br />

Foreign exchange risk occurs as a result of transactions denominated in a currency other than ESR’s functional<br />

currency of NZD. Currencies commonly transacted in and giving rise to foreign exchange risk include the<br />

US dollar, Australian dollar and the pound sterling. ESR is subject to foreign currency risk through its trade<br />

receivables and trade payables balances.<br />

Where a material foreign currency balance is entered into (exposures equivalent to greater than NZD<br />

$100,000), ESR is required by the Treasury Management Policy to hedge its exposure to the currency through<br />

the use of forward exchange contracts.<br />

ESR held no forward exchange contracts at 30 June <strong>2011</strong> (30 June 2010: Nil).<br />

The carrying amounts of the Group’s trade and other receivables are denominated in the following currencies:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Australian dollar 31 112<br />

Euro 16 –<br />

US dollar 34 26<br />

Other – 57<br />

81 195<br />

The carrying amounts of the Group’s trade and other payables were denominated in the following currencies:<br />

Group Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s $’000s<br />

Australian dollar 58 2<br />

Canadian dollar 9 –<br />

US dollar 8 8<br />

Other 10 1<br />

85 11<br />

ii) Interest rate risk<br />

As at reporting date, ESR is subject to interest rate risk through the holding of cash and cash equivalents. ESR<br />

uses a mixture of call and short-term deposit investment accounts to hold excess funds. Available interest rates<br />

are monitored to ensure the best return on cash.<br />

When ESR is required to draw down its credit facilities, interest rate risk is managed through entering into a<br />

predetermined mixture of floating and fixed rate borrowings, depending on the level of borrowings entered into.<br />

ESR did not have any borrowings as at 30 June <strong>2011</strong> (30 June 2010: Nil).<br />

iii) Market risk sensitivity analysis<br />

ESR is exposed to market risk through the holding of the following financial instruments: cash, trade receivables<br />

and trade payables. ESR management has analysed the below sensitivities in market risk factors over a 12-month<br />

period:<br />

• Proportional foreign exchange rate movement of -10% (depreciation of NZD) and +10% (appreciation of<br />

NZD) against the foreign currencies; and<br />

• A parallel shift of +1% / -1% in market interest rates in New Zealand.<br />

If these movements were to occur (all other variables held constant), the impact on ESR’s reported profit before<br />

income tax expense and equity at balance date is presented below.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 65


Group<br />

30 JUNE 2010<br />

Carrying Interest rate Foreign exchange<br />

amount -100bp +100bp -10% +10%<br />

$’000s Profit Equity Profit Equity Profit Equity Profit Equity<br />

Financial assets<br />

Cash and cash equivalents 6,938 (69) (69) 69 69 – – – –<br />

Trade receivables 195 – – – – (20) (20) 18 18<br />

Financial liabilities<br />

Trade payables 11 – – – – (1) (1) 1 1<br />

Total (decrease) / increase (69) (69) 69 69 (21) (21) 19 19<br />

Group<br />

30 JUNE <strong>2011</strong><br />

Carrying Interest rate Foreign exchange<br />

amount -100bp +100bp -10% +10%<br />

$’000s Profit Equity Profit Equity Profit Equity Profit Equity<br />

Financial assets<br />

Cash and cash equivalents 7,501 (75) (75) 75 75 – – – –<br />

Trade receivables 81 – – – – 8 8 (7) (7)<br />

Financial liabilities<br />

Trade payables 85 – – – – (8) (8) 8 8<br />

Total (decrease) / increase (75) (75) 75 75 – – 1 1<br />

b) Credit risk<br />

Credit risk refers to the risk that a counterparty will default on its contractual obligations, resulting in<br />

financial loss to ESR. The financial instruments, which expose ESR to credit risk, are principally cash and cash<br />

equivalents, and trade receivables.<br />

Bank balances and short-term investments (comprising cash and cash equivalents) are held with New Zealand<br />

registered banks in accordance with ESR’s Treasury Management Policy. The majority of high-value trade<br />

receivables comprise government entities and therefore the potential risk of default is low. ESR has a Contracts<br />

Policy that requires assessments of the credit worthiness of potential clients, where the value of a contract is<br />

material as defined in the Policy.<br />

A provision for doubtful debts is maintained in respect of trade receivables and this is reassessed on a regular<br />

basis. No collateral is held by ESR in respect of cash and cash equivalents, and trade receivables as at 30 June<br />

<strong>2011</strong> (30 June 2010: Nil).<br />

The carrying amount of financial assets recognised in the Statement of Financial Position best represents ESR’s<br />

maximum exposure to credit risk at the reporting date.<br />

As at 30 June <strong>2011</strong> the trade receivables balance included $8,573,000 (30 June 2010: $9,831,000) owed by<br />

entities within, or owned by, the New Zealand Government. It is not believed that there is any material risk of<br />

loss with these receivables.<br />

c) Liquidity risk<br />

Prudent liquidity risk management implies the availability of funding through adequate levels of committed<br />

credit facilities. Liquidity risk is monitored through the forecasting of cash flows, and ensuring that the<br />

committed credit lines in place remain adequate for requirements.<br />

A contractual discounted maturity analysis of financial liabilities is presented below:<br />

Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

Less Greater Less Greater<br />

Carrying than 1-2 2-5 than 5 Carrying than 1-2 2-5 than 5<br />

value 1 year years years years value 1 year years years years<br />

$’000s $’000s $’000s $’000s $’000s $’000s $’000s $’000s $’000s $’000s<br />

Trade payables 8,460 8,460 – – – 9,442 9,442 – – –<br />

Finance lease liabilities 293 178 90 47 – 296 199 102 15 –<br />

8,753 8,638 90 47 – 9,738 9,641 102 15 –<br />

As at 30 June <strong>2011</strong>, ESR had no derivative financial instruments (30 June 2010: Nil).<br />

66 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


d) Fair values<br />

The carrying value of financial assets and liabilities recorded in the financial statements approximate their fair<br />

values.<br />

Fair value is generally based on the contracted amount payable / receivable of financial assets and financial<br />

liabilities, being the amount for which the financial instrument is to be exchanged. Fair value includes the<br />

impact of any assessed impairment of the financial instruments – please refer to the Statement of Significant<br />

Accounting Policies for details of each financial instrument and their recognition criteria.<br />

e) Capital risk management<br />

ESR’s objectives when managing capital are to maintain financial stability, achieve sustainable growth and to<br />

realise its strategic goals and targets, all within the risk appetite of its shareholder and management.<br />

In line with Government requirements, ESR monitors its capital structure through the return on equity and<br />

gearing ratios. The Government provides ESR with guideline targets with the expectation that an appropriate<br />

average return will be achieved over time, rather than requiring that ESR meet the specified targets annually.<br />

At reporting date, the Government-provided guideline targets are 9% for the return on equity, and 30% for the<br />

gearing ratio, (2010: same).<br />

Each year ESR internally sets return on equity and gearing ratio targets, bearing in mind the overall results<br />

expected by the Government. The ratios are reported in the Statement of Corporate Intent.<br />

The return on equity and gearing ratios as at 30 June <strong>2011</strong> and 30 June 2010 were as follows, along with the<br />

relevant annual targets set by ESR.<br />

The return on equity ratio was affected by the change in tax legislation enacted on 27 May 2010, which<br />

eliminated tax depreciation on buildings.<br />

Return on equity ratio<br />

Group<br />

Group<br />

30 June <strong>2011</strong> 30 June 2010<br />

$’000s<br />

$’000s<br />

Profit / (loss) for the year 3,222 (518)<br />

Average equity 33,869 32,517<br />

Actual ratio 9.5% (1.6%)<br />

Target ratio 8.0% 8.0%<br />

Gearing ratio<br />

Net debt<br />

Finance lease liabilities – current 164 190<br />

Finance lease liabilities – non current 129 106<br />

293 296<br />

Equity 35,480 32,258<br />

Actual ratio 0.8% 0.9%<br />

Target ratio 0.0% 0.0%<br />

24. Contingent liabilities<br />

The directors are satisfied that there are no claims outstanding that would have a material impact on ESR’s<br />

financial position, as at 30 June <strong>2011</strong> (30 June 2010: Nil).<br />

25. Subsequent events<br />

There were no events subsequent to reporting date that require disclosure in the financial statements.<br />

ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong> | 67


Registered office<br />

Kenepuru <strong>Science</strong> Centre<br />

34 Kenepuru Drive<br />

PO Box 50 348<br />

Porirua 5240<br />

New Zealand<br />

Telephone: +64 4 914 0700<br />

Fax: +64 4 914 0770<br />

Auditor<br />

Chris Barber of PricewaterhouseCoopers on<br />

behalf of the Auditor-General<br />

Banker<br />

The National Bank of New Zealand Limited<br />

Solicitor<br />

Buddle Findlay<br />

68 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>


70 | ESR <strong>Annual</strong> <strong>Report</strong> <strong>2011</strong>

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