EuroMEEting - Genetic Alliance UK
EuroMEEting - Genetic Alliance UK
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