|Project Title||Medical Product Safety: Ten Years of the U.S. Sentinel System|
Thursday, May 23, 2019
This presentation discussed the creation of the U.S. Sentinel System, the data contained within it and how such data are curated, the FDA's use of the Sentinel System for safety/regulatory questions, methods development, and advances in the FDA-Catalyst program that supports studies that include patient interventions.
The presentation was originally given as a webinar and is available for viewing. To access the webinar:
Sarah Dutcher, Judith C. Maro, David Martin
- Vaccines, Blood & Biologics
- Devices and Radiologic Health