European Information Network - Ethics in Medicine and Biotechnology
A project of the European Commission,Quality of Life and Management of Living Resources Programme
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European Information Network - Ethics in Medicine and BiotechnologyA project of the European Commission,Quality of Life and Management of Living Resources Programme |
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If you require further information, please contact the organizers directly.
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| Date: | 27.04.2010, 17:15h to 28.04.2010, 16:20h |
| Location: | Crowne Plaza Antwerp
G. Le Grellelaan 10
2020 Antwerp
Belgium Antwerpen Belgien |
| Keywords: | Ethics committees - Research ethics committees - End of life - Medical ethics |
| Details: | Medical research and drug development are focused typically on an adult population of patients frequently excluding, at one end of the age spectrum, children and, at the other, the elderly and frail. Reasons for these exclusions are multiple and are not the same for both populations, but typical hurdles are shared as e.g. ethical concerns about informed consent, the need for specific formulations, specific adaptations of protocol procedures etc. Therefore these vulnerable populations are today unrepresented in research and drug development. Once a drug is on the market and used, clinicians, patients and caregivers have to base their treatment decisions on empiric data and dose assumptions and not on scientific valid data. This lack of data was already identified in the past, but specifically only for children. Thus drug development regulatory bodies, academia, researchers and patients’ advocacy groups have recently agreed on improved and clear guidelines for research involving children. Much to be welcomed is the recently implemented, and in force in Europe since 2008, Paediatric Investigational Plan (PIP) for all new drugs in development. At the other end of life, for the older and frail people, a lot of effort has still to be done as existing international recommendations and regulations are under review and the next steps to define what they will yield and how they will improve the situation are under discussion. The European Forum for Good Clinical Practice (EFGCP) and The European CRO Federation (EUCROF) have thus brought together experts from both fields, experts in clinical research, ethics, social, patient organisations and pharmaceutical regulatory bodies to explore the shared ethical issues and to learn lessons from each other. The objective of this workshop is to share concerns, to detect possible synergies and to learn from each other in order to improve and to facilitate and promulgate high quality ethical clinical research and drug development for these important populations across the whole of the European Union. |
| Organizer: | Organised by EFGCP & the European CRO Federation (EUCROF) |
| Contact: | Address: EFGCP Secretariat Square de Meeûs Rue de l'Industrie 4 1000 Brussels Belgium Tel: +32 - (0)2 - 7 32 87 83 Fax: +32 - (0)2 - 5 03 31 08 Email: conferences@efgcp.be |
| Webpage: | http://www.efgcp.be/Conference_details.asp?id=267&L1=10&L2=1&TimeRef=1 |
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