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EU simplifies GMP template for investigational drugs

This article was originally published in SRA

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Executive Summary

The European Commission has simplified the means by which companies can certify that investigational drugs from non-EU countries comply with good manufacturing practice standards1.

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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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