MedWatch Adverse Event Reporting Program

The next webinar presented by the Division of Drug Information will provide an introduction to the FDA’s MedWatch Adverse Event reporting program. Participants will learn how and why to report adverse events to the MedWatch program, and where to find clinically relevant information from MedWatch. They’ll also have the ability to earn CME credit.

The webinar will take place Tuesday, January 26, 2-3 p.m. (EST). Register now.