Drug Safety and Pharmacovigilance Across the Product Lifecycle
Build a solid foundation in the key concepts of drug safety and pharmacovigilance throughout the medical product development lifecycle. Learn how to comply with regulatory requirements.
Session 15: Post-Marketing Safety Regulations – EU
Jill W. Buckley, PharmD
- Adjunct Assistant Professor
- Rutgers, the State University of New Jersey, United States
This session will discuss EU Good Pharmacovigilance Practices (GVP) which are a set of measures drawn up to facilitate the performance of the safety monitoring of medicines in the European Union.