Adverse Event Reports: Posting On ClinicalTrials.gov Begins Soon
By
Jessica Bylander / Email the Author / “The Gray Sheet” Apr. 27, 2009, Vol. 35, No. 017
Regulatory / Word Count: 600 / Article # 01350170005
Executive Summary
Device and drug firms must begin posting serious and frequent adverse event data from certain clinical trials on the National Institutes of Health's ClinicalTrials.gov database by September, NIH confirmed April 20
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