Date

Monday, 06 September 2010

Location

European Medicines Agency, Amsterdam, the Netherlands

The workshop is enabling participants to discuss and provide feedback on the 'Draft reflection paper on ethical and good-clinical-practice aspects of clinical trials of medicinal products for human use conducted in third countries and submitted in marketing authorisation applications to the European Medicines Agency', which was released for public consultation in May 2010. The workshop complements this consultation process. Registration closed.

Documents

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