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EMA to make public side-effects in EudraVigilance database by end of 2011

This article was originally published in SRA

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Executive Summary

The European Medicines Agency by the end of 2011 plans to start granting public access to information in its EudraVigilance database on potential side-effects of certain human drugs1.

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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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