Live Demo of the FDA Adverse Events Reporting System (14/14) REdI 2017 скачать в хорошем качестве

Live Demo of the FDA Adverse Events Reporting System (14/14) REdI 2017

Sanjay K. Sahoo provides a live demonstration on how to use the dashboard. To increase transparency at FDA, the agency has developed an interactive application for public access. The FDA Adverse Events Reporting System (FAERS) Public Dashboard is an interactive application, which enables the public to search for information related to human adverse event drug reports (ADRs) reported to the FDA by the pharmaceutical industry, healthcare providers and consumers. ------------------------- 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 2017 Playlist:    • 2017 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