Regulatory agencies are requiring stricter standards for environmental monitoring systems, facility cleaning and disinfectant qualification, aseptic cleanroom operations, filtration, sterilization, and aseptic process simulation (or media fill). This two-day summit features comprehensive coverage of best practices in barrier, containment, and aseptic manufacturing and processing technologies.

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, med devices, and their 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 parenteral product development, and the complex quality, safety, and regulatory compliance issues facing the industry.