Successful conference on clinical drug trials
30. September 2016
Download the Conference Report here
Four central issues have been debated by prominent international experts:
- Globalisation of clinical trials and ethics
- Transparency and access to data
- Evidence generation for marketing authorisation and adaptive pathways
- The way forward for needs-driven biomedical research.
The often incomplete and selective data communicated around clinical trials are the subject of intense discussions. According to Patrick Durisch, full transparency should “be the rule, not the exception”. It is hoped that the conference allows to “raise the alarm for stricter regulation of clinical trials”.
Conference material
Presentations
- Keynote Tom Jefferson, Centre for Evidence Based Medicine
- Keynote Teresa Alves, La Revue Prescrire
- Keynote Ruth Dreifuss, High-Level Panel on Access to Medicines
Globalisation of clinical trials and ethics:
- Patrick Durisch, Public Eye
- Ayman Sabae, Egyptian Initiative for Personal Rights
- Samia Hurst, University of Geneva
- Françoise Jaquet, Swissmedic
Transparence and access to data :
- Tom Jefferson, Centre for Evidence Based Medicine
- Jan Stadler, European Ombudsman
- Ancel.la Santos, HAI
- Ghassan Karam, WHO
Marketing authorisation & adaptive Pathways:
- Hans Georg Eichler, EMA
- Beate Wieseler, IQWiG
- Joerg Schaaber, ISDB BUKO
- Monica Cavagna, BEUC
- Sopie le Pallec, Amalyste
Way forward to a needs-driven biomedical research:
- Silvio Garattini, Mario Negri Institute
- Joel Lexchin, York University CAN
- Katy Athersuch, MSF Access Campaign
- Nathalie Strub, DNDi
Further information about Clinical Trials.