<%@LANGUAGE="VBSCRIPT" CODEPAGE="1252"%> Untitled Document

EU Clinical Trials Directive

EU Clinical Trials Directive 2001/20/EC
Written submission on the operation of the Clinical Trials Directive and perspectives for the future - ECRIN, EORTC, ESF-EMRS, CPI, INSERM, VISEAR and ESICM's position
Report on the European Commission-EMEA Conference on the EU Clinical Trials Directive - October 3, 2007
Report on the EORTC-CONTICANET-ICREL-ECRIN Workshop "Biomedical Research in Europe: Which Challenges and Solutions for Academic Sponsors?" May 21st, 2008, EORTC Headquarters, Brussels, Belgium"

For any further information, please contact:
Diane van Vyve, MLaw
EORTC Regulatory Legal Advisor
Tel: +32 (0)2 774 16 79
Fax: +32 (0)2 772 80 27
e-mail: diane.vanvyve@eortc.be

	EORTC AISBL / IVZW Avenue Mounierlaan, 83/11 Brussel 1200 Bruxelles • Belgie Belgique +32 2 774 16 11
Visitors • Investigators • Intranet • Home

EU Clinical Trials Directive

EU Clinical Trials Directive 2001/20/EC

Written submission on the operation of the Clinical Trials Directive and perspectives for the future - ECRIN, EORTC, ESF-EMRS, CPI, INSERM, VISEAR and ESICM's position

Report on the European Commission-EMEA Conference on the EU Clinical Trials Directive - October 3, 2007

Report on the EORTC-CONTICANET-ICREL-ECRIN Workshop "Biomedical Research in Europe: Which Challenges and Solutions for Academic Sponsors?" May 21st, 2008, EORTC Headquarters, Brussels, Belgium"