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 4: Clinical Trial Safety Regulations – US IND Safety Reporting

Session Chair(s)

Jill W. Buckley, PharmD

• Adjunct Assistant Professor
• Rutgers, the State University of New Jersey, United States

This session will cover the FDA requirements for safety reporting for clinical trials.