FDA Adverse Event Reporting System (FAERS) Overview - Pharmacovigilance 2020 скачать в хорошем качестве

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 understanding the regulatory aspects of human drug products & clinical research. Upcoming training and free continuing education credits: https://www.fda.gov/cdersbia CDER SBIA 2020 Playlist:    • 2020 CDER Small Business and Industry Assi...   LinkedIn:   / cder-small-business-and-industry-assistance   Training resources: https://www.fda.gov/cderbsbialearn Twitter:   / fda_drug_info   CDER small business e-mail update subscription: https://updates.fda.gov/subscriptionm... Email: [email protected] Phone: (301) 796-6707 I (866) 405-5367