EuroMEEting - Genetic Alliance UK

More documents

Recommendations

Info

14 TUTORIALS This is the advance programme. New speakers and sessions will be added. Visit www.diahome.org for the most recent additions to the programme. Pre-Conference Tutorials | Monday, 28 March 2011 | 09:00 - 12:30 Target Audience • Hospital pharmacists • Physicians, in particular oncologists, where this approach is common • Pharmaceutical company executives with responsibility for pricing, reimbursement and market access Tutorial 16 INTRODUCTION TO CRISIS MANAGEMENT Jan-Willem van der Velden, CEO, Founding Director, Mesama Consulting, Switzerland Michael Forstner, Integrated Safety Risk Manager, F. Hoffmann-La Roche Ltd., Switzerland In this introductory tutorial the participant will be made familiar with the definition of a crisis and understand which processes in their own working environment could be vulnerable for possible crises. Examples are given and participants are invited to join in exercises and learn which parties are all involved within and outside their organisation. The participant will be provided with the tools with which to plan for a potential crisis and how to build a preventive strategy. The roles of the Crisis Management Team members are shown and examples are given of right and wrong actions, including attitude towards the media. Learning Objectives At the conclusion of this tutorial, participants will be able to: • Distinguish between an issue, a risk and a crisis and recognize the flow of events that lead from an issue to a crisis • Recognise a potential crisis on time and approach a crisis appropriately when it happens • Set up a crisis team that should be able to deal with the crisis in all its stages Target Audience • Regulatory authorities • PV experts • Pharmaceutical industry • Medical affairs • Drug safety department • Marketing department • Legal department • Corporate communications department Tutorial 17 INCENTIVES TO DRUG DEVELOPMENT: EXPAND YOUR REGULATORY INTUITION Zaide Frias, Head of Regulatory Affairs, European Medicines Agency, EU Christelle Bouygues, Regulatory Affairs Advisor, European Medicines Agency, EU This tutorial will present, in the light of an ever-changing EU legislative environment, the recent incentives to drug development which are of scientific, financial and regulatory procedural nature or a combination of those. The tutorial will cover in detail the various data exclusivity provisions, the orphans, paediatrics and ATMPs incentives as well as provide an insight into the experience with the operation of “early access tools” such as the accelerated review, the conditional and exceptional circumstances MAs by EMA/CHMP. Each aspect will be applied in practice through interactive case studies. Learning Objectives At the conclusion of this tutorial, participants will be able to: Having a detailed knowledge and early consideration of these incentives and tools should enable the participants to expand their regulatory intuition; as a result: • Anticipate, plan and streamline the milestones for their drug development and registrations • Develop a sound regulatory strategy optimizing the use of the various incentives and tools provided for. • Discuss advantages and disadvantages of different regulatory strategies for their business pipeline with concerned regulatory authorities Target Audience • All persons involved in business intelligence, regulatory affairs, business pipeline and regulatory authorities. Continuing Education DIA Europe has applied for credits from the Faculty of Pharmaceutical Medicine (FPM) of the Royal College of Physicians (RCP) of the <strong>UK</strong>. DIA Europe's meetings are accredited by the SwAPP (Swiss Association of Pharmaceutical Professionals) Commission for Professional Development and SGPM (Swiss Society of Pharmaceutical Medicine). Always Stay One Move AheadWith DIA Training Courses The Best Value Training Available Anywhere. First-rate instructors and best-in-class content are what make DIA’s training programmes the highest quality training programmes available anywhere. DIA offers a variety of courses in regulatory affairs, clinical research, non-clinical safety sciences and pharmacovigilance. Benefits include: • Expert instructors actively practicing in their particular discipline • Continuing education credits • Up-to-the-minute coverage of important industry hot topics • Networking opportunities • Consistent course materials from one offering to another • Limited attendance allows for a more personal quality learning experience • Tailor-made case studies and instructor-led group work • In-depth discussion of specific contemporary issues For more information and a complete listing of all training courses, please visit www.diahome.org and click on Training.
GREENING THE EUROMEETING 15 GREENING THE EUROMEETING TOWARDS AN ENVIRONMENTALLY FRIENDLY CONFERENCE Geneva is a city which takes its responsibility for the environment seriously, from renewable energy production to its efficient public transport system. This commitment to the environment extends to the Palexpo Convention Centre who share the DIA’s commitment to an environmentally-friendly EuroMeeting. Waste recycling for some events at Palexpo has now reached levels of nearly 80%. Other measures include the provision of all of Palexpo’s energy needs by hydro-electric power and/or solar panels on the roof of one of the halls and an electrical charge port for two-wheel vehicles in the parking area which may be used free of charge. Using practical, innovative, and often very simple measures, the EuroMeeting’s carbon footprint has been successfully reduced. We will be practicing the 3Rs in Geneva: Reduce, Recycle and Reuse. We will offer you an environmentally-friendly conference bag when you collect your badge (which of course, we will recycle at the end of the meeting if you return it to us). Recycling bins will be placed throughout the building. The meeting will be paperless wherever possible, and all EuroMeeting publications will be printed on FSC-certified paper, which means that they are sourced from well-managed forests and recycled wood. Working with exhibitors is an important part of the EuroMeeting, and we look forward to a successful partnership in 2011. The Greenest Exhibitor Award, now in its third year, aims to raise the awareness of exhibitors of this growing movement in the conference and exhibitions industry. We make it easy for exhibitors to recycle. Additionally, we ensure that stand carpets, for example, are recycled for use in other products such as pots and containers, and untreated wood is compacted, to be reused as medium-density fibreboard panels used by furniture manufacturers. The European office members will travel to the 2011 EuroMeeting by train. DIA will offset the air miles of other staff travelling to the EuroMeeting with a Swiss non-profit foundation, "myclimate" – The Climate Protection Partnership (www.myclimate.org), and we encourage all our participants and exhibitors to support our greening initiative by considering offsetting their miles. All participants will receive a free Geneva public transport card when checking in at their hotels. This promotion of public transportation helps to reduce congestion as well as pollution. We commit to not using disposable cups, plates or cutlery. There will be water coolers throughout the building, reducing the need for individual bottles of water. Locally grown food will be used wherever possible with participants able to eat healthily as low down the food chain as possible, with vegetarian options on offer. If you have any suggestions or creative ideas on how we could do more, please contact Dermot Ryan, EuroMeeting Manager at dermot.ryan@diaeurope.org.
Page 1 and 2: EuroMEEting gEnEva 2011 28-30 March
Page 3 and 4: EUROMEETING 2011 CO-CHAIRS’ MESSA
Page 5 and 6: PLAN YOUR EUROMEETING EXPERIENCE 5
Page 7 and 8: SPECIAL SESSIONS 7 This is the adva
Page 9 and 10: DIA FELLOWSHIPS 9 This is the advan
Page 11 and 12: TUTORIALS 11 This is the advance pr
Page 13: TUTORIALS 13 This is the advance pr
Page 17 and 18: THEME 1 | THEME 2 17 This is the ad
Page 19 and 20: THEME 2 19 This is the advance prog
Page 33 and 34: THEME 10 33 This is the advance pro
Page 37 and 38: THEME 12 | THEME 13 37 This is the
Page 39 and 40: THEME 13 | THEME 14 39 This is the
Page 43 and 44: HOT TOPICS | STAND ALONE SESSIONS 4
Page 45 and 46: ABOUT GENEVA 45 This is the advance
Page 47 and 48: ACCOMMODATION AND TRANSPORT 47 This
Page 49 and 50: D I A 2011 Convergence of Science M
Page 51 and 52: Lunch Lunch 23RD ANNUAL EUROMEETING
Page 53 and 54: EuroMeeting Key Contacts Go to the

EuroMEEting - Genetic Alliance UK

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?