Ensuring Quality, Safety, Suitability and Regulatory Compliance for Drugs, Biologics and Medical Devices
- Two full days of presentations, panel discussions, and networking
- The industry’s top experts share their knowledge and lessons learned
- Learn what you need to know to meet regulatory expectations for E/Ls in drug products, delivery systems, medical devices, and packaging
- Focus on overcoming common analytical challenges in E/L study design
- Gain insight into AET’s and uncertainty factors in E/L analysis
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