Webinar: FDA’s MedWatch Adverse Reporting Program – Opportunities to Collaborate
On Tuesday, March 13, at 1:00 p.m. ET, join the FDA’s Division of Drug Information for a webinar on their MedWatch Adverse Reporting Program and ways to collaborate and get involved. Specifically, the webinar will cover:
- Information about the FDA Office of Health and Constituent Affairs (OHCA)
- Ways to collaborate and be involved in FDA processes
- Adverse events and product problems that should be reported to FDA
- How to submit a report to the FDA MedWatch Program
This free session will be presented by Steve Morin, RN, BSN, health programs coordinator in FDA’s Office of Health and Constituent Affairs. To register, please visit the FDA website.