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EU Clinical Trials Directive & Impact on Clinical Research

DIRECTIVE 2001/20/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use.

REPORT of the Multidisciplinary Workshop "Towards A Better Future for Pharmacovigilance in Clinical Trials", 8th February 2010, EORTC Headquarters, Brussels

Final Report of the FP7 project ICREL «Impact on Clinical Research of European Legislation»

For any further information, please contact:
Stéphane Lejeune , MPH
EORTC, EU Programme Officer
Tel: +32 (0)2 774 10 75
Fax: +32 (0)2 772 35 45
e-mail: stephane.lejeune@eortc.be