Pharmacovigilance
About Course
This module explains U.S. pharmacovigilance systems, emphasizing adverse event (AE) reporting timelines, serious AE criteria, and FDA’s FAERS database. Participants will learn to identify AEs, handle product complaints, and comply with post-marketing surveillance requirements to avoid regulatory penalties.
Suggested For:
- Compliance Officers
- Compliance Teams
- Field Based Sales Professionals
- Medical Science Liaisons
- Medical Affairs Personnel
- Marketing Personnel
- Regulatory Affairs
- Legal Teams