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48:21
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U.S. Food and Drug Administration
FDA Adverse Event Reporting System (FAERS) Overview - Pharmacovigilance 2020
Suranjan De, Deputy Director for CDER’s Regulatory Science Staff (RSS), describes FAERS data content, the Individual Case Safety Report (ICSR) submission process, and public access to data through the FAERS dashboard. _______________________________ FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in ...
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Jun 15, 2020
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