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EuroMEEting - Genetic Alliance UK

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SPECIAL SESSIONS<br />

7<br />

This is the advance programme. New speakers and sessions will be added. Visit www.diahome.org for the most recent additions to the programme.<br />

Student Sessions<br />

Session 1701 | Monday, 28 March 2011 | 09:00-09:40<br />

PRESENT WITH CONFIDENCE WORKSHOP<br />

Instructor: Judy Churchill, Communication Skills Specialist, France<br />

Session 1702 | Monday, 28 March 2011 | 09:50-10:30<br />

CURRICULUM VITAE WORKSHOP<br />

Instructor: To be confirmed<br />

Students attending this workshop will receive tips and advice on creating a<br />

winning CV.<br />

Session 1703 | Monday, 28 March 2011 | 11:00-12:30<br />

DIA STUDENT CHAPTER SESSION<br />

2015 Roadmap Session<br />

Session 1603 | Tuesday, 29 March 2011 | 14:00-15:30<br />

Session Chair:<br />

Noel Wathion, Head of Public Health Protection, European Medicines Agency,<br />

EU<br />

On 26 January 2010, the European Medicines Agency published a draft paper<br />

setting out its vision for the strategic development of the Agency for the five<br />

years to 2015. Building on the progress of its previous five-year strategy, the Road<br />

Map to 2015 charts the way forward for the Agency amid rapid developments<br />

in medical science and pharmaceutical research, as well as the continuing<br />

evolution of the European and international regulatory environments. With this<br />

strategy paper to guide it, the Agency will seek to consolidate its achievements<br />

to date and further strengthen its role as a guardian of human and animal health<br />

in the European Union.<br />

Emer Cooke, International Liaison Officer, European Medicines Agency, EU<br />

in partnership with the European Pharmaceutical Students’<br />

Association (EPSA) and the International Federation of<br />

Medical Students’ Associations (IFMSA).<br />

All student participants are invited to join an informal networking and<br />

information session in which they can learn more about a range of professional<br />

disciplines in the pharmaceutical world: What do they involve? What is the best<br />

way in? What are the challenges and the opportunities?<br />

Taking the innovative form of an interactive attendee-led “unconference”, which<br />

does not have any agenda, speakers or presentations, participants begin by<br />

discussing what they would like to get out of the session and what topics of<br />

interest they would like to see covered. A group of experienced professionals<br />

from a range of pharmaceutical backgrounds will lead small groups of students<br />

in discussion around the room. There will be an open format and students may<br />

move from one group to another.<br />

Young Professionals Session<br />

Session 1800 | Monday, 28 March 2011 | 11:00-12:30<br />

Session Chair:<br />

Estelle Michael, Senior Manager Regulatory Policy and Intelligence,<br />

GlaxoSmithKline, Biologicals, Belgium<br />

Currently under development.<br />

Heads of Medicines Agencies Session<br />

Session 1602 | Tuesday, 29 March 2011 | 11:00-12:30<br />

Session Chair:<br />

Kent Woods, Chief Executive, MHRA, <strong>UK</strong><br />

Jean Marimbert, General Director, Afssaps, France<br />

Jytte Lyngvig, Chief Executive Officer, Danish Medicines Agency, Denmark<br />

Session under development<br />

Town Hall Meeting<br />

Session 0206 | Wednesday, 30 March 2011 | 11:00-12:30<br />

MEET THE REGULATORS<br />

Moderator:<br />

Christa Wirthumer-Hoche, Deputy Head, AGES PharmMed, Austria<br />

The Town Hall Meeting is an open interactive session where participants can<br />

ask key decision makers in the European Regulatory system burning questions.<br />

The panel will include representatives from the European Medicines Agency,<br />

National Competent Authorities and a patient organisation.<br />

The topics/questions discussed are decided by the attendees and should be<br />

related to:<br />

• Responsibility of the Agencies in the EU network<br />

• Authorisation and Maintenance of Medicinal Products; Benefit/Risk<br />

Methodologies<br />

• Pharmacovigilance<br />

• International Cooperation and Inspection-Related Issues<br />

• Electronic Submission<br />

• The Role of Patient Organisations<br />

Responsibilities of the Agencies in the EU Network<br />

Noel Wathion, Head of Public Health Protection, European Medicines Agency,<br />

EU<br />

Aginus Kalis, Chair HMA-MG, Executive Director, Medicines Evaluation Board<br />

(MEB), The Netherlands<br />

Authorisation and Maintenance of Medicinal Products; Benefit/Risk<br />

Methodologies<br />

Hans-Georg Eichler, Senior Medical Officer, European Medicines Agency, EU<br />

Eric Abadie, Chair CHMP, Chair Pharmacogenomics Working Party, General<br />

Director, Afssaps, France<br />

Truus Janse-de Hoog , Chair CMD(h), Staff member MEB, European cluster,<br />

Medicines Evaluation Board, The Netherlands<br />

Aginus Kalis, Executive Director, Medicines Evaluation Board (MEB), The<br />

Netherlands<br />

Marcus Muellner, Director, AGES PharmMed, Austria

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