The Implementation of Directive 2001/20/EC in Europe
English translation (slightly amended) of a paper which appeared in the Tijdschrift voor Gezondheidsrecht, volume 33, number 6 (October, 2009)
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Tags: clinical trials, collaboration, Directive 2001/20/EC, drugs, ethical review boards, ethics, ethics research committees, EU law, European harmonisation, European research, implementation, insurance, investigator initiated research, medical research, non commercial research, sponsor, trial subjects, WMO