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EMA consults on trial database transparency challenge

This article was originally published in Scrip

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Executive Summary

In the latest stage in the EU's efforts to widen the publication of clinical trial data, the European Medicines Agency has opened a public consultation on how to decide exactly what information should be available in the future clinical trials database, which will be accessible to the general public.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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