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US FDA blazes the transparency trail

This article was originally published in SRA

Executive Summary

There has been no shortage of moves to increase transparency at regulatory agencies in the past year or so. The European Medicines Agency has brought in new policies on access to documents and clinical trial data, while side effect data are to be made more easily available. The French regulator, meanwhile, has promised zero tolerance on conflicts of interest among its committee members and more transparency on publishing minutes of its committee meetings.

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