This two-day conference examines the keys to satisfying several applicable USP chapters, FDA guidances, and other international regulatory requirements for best practices in materials and chemistry characterization for drugs, biologics, delivery systems, and primary & secondary packaging
Advances in digital health and connected devices are revolutionizing the parenteral drug delivery landscape. This two-day summit features expert insight into next-generation CP product development, and the complex quality, safety, and regulatory compliance issues facing the industry. Pharma Ed’s Pre-filled Syringes & Injection Devices 2024: Exploring the Future of Parenteral Combination Products provides comprehensive coverage of current and future trends in combination product development for parenteral delivery platforms and devices.
Can you implement the best science-, risk-, and statistics-based approaches to cleaning validation? Today’s regulators are now expecting ADE monographs and comprehensive risk assessments of your organization’s cleaning validation protocols. Pharma Ed’s Cleaning Validation Summit brings together leading industry experts to illuminate best practices, help you meet regulatory requirements, and provide practical insights into avoiding costly mistakes.