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BioPharmaceutical United States Regulation

FDA Reprint Policy Expands To Clinical Practice Guidelines, Medical Reference Texts

This article was originally published in The Pink Sheet Daily

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Executive Summary

FDA has revised, but not loosened, its 2009 final guidance on good reprint practices for distribution of journal articles on unapproved uses of approved drugs and devices.

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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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