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Publishing individual patient data from trials: EMA considering how and when

This article was originally published in SRA

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Executive Summary

The European Medicines Agency's policy on proactive publication of clinical trial data, which currently pertains to clinical study reports from approved drugs, will eventually be expanded to allow access to individual patient data.

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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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