FDAnews Announces — New Book — Clinical Trials Adverse Event Reporting...

The FDA requires clinical trial sponsors to report any patient’s serious adverse drug reaction if the sponsor determines that the “information qualifies for reporting” under section 312.32 of its...(PRWeb October 09, 2017)Read the full story at http://www.prweb.com/releases/FDAnews/ctadverseeventreporting/prweb14756180.htm
Source: PRWeb: Medical Pharmaceuticals - Category: Pharmaceuticals Source Type: news