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

This article was originally published in The Pink Sheet Daily

15 Feb 2016
News

Brenda Sandburg @brendasandburg Brenda.Sandburg@informa.com

Executive Summary

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

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Topics

Industries
BioPharmaceutical
Regions
North America

United States

Subjects
Regulation

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

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