Start: Tuesday, July 15, 2025 9:00AM
End: Wednesday, July 16, 2025 5:00PM
Join industry leaders to explore the evolving role of Risk Evaluation and Mitigation Strategies (REMS) in drug safety. Participate in in-depth sessions and case studies on patient-centric, FDA-compliant REMS programs, cross-functional collaboration, and technology-driven risk management. Designed for professionals in Benefit/Risk Management, Quality Assurance, and Regulatory Affairs. Don't miss this chance to connect with peers and advance medication safety.
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