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BioPharmaceutical United States Regulation

FDA's Temple To Industry: Don't Send In Every Adverse Event Report

This article was originally published in The Pink Sheet Daily

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Executive Summary

Robert Temple offers advice on how to avoid 'a waste of everybody's time' during IND safety reporting.

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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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