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Ensuring Quality, Safety, Suitability, & Regulatory Compliance for Drugs, Biologics and Medical Devices

November 11-12, 2021, San Diego, (Hybrid)

From PharmaEd’s website:

This two-day conference will examine the safety, quality, and regulatory issues involved in a wide array of contexts central to the pharmaceutical and biotech industries, including drug packaging and delivery components, single-use systems, medical devices, and parenteral drug products. In addition, we will focus closely on the keys to satisfying recent revisions to several applicable USP chapters, ICH Q3E, and the recently revised standards contained in ISO 10993.