Can you implement the best science-, risk-, and statistics-based approaches to cleaning validation? Today’s regulators are now expecting HBEL monographs and comprehensive risk assessments of your organization’s cleaning validation program. 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.

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. We will focus closely on the keys to satisfying recent revisions to several applicable USP chapters, FDA guidances & other international regulatory requirements for best practices in materials and chemistry characterization for drugs, biologics, delivery systems, and primary & secondary packaging.