“Your conference is one of my favorites and one of the few where I feel like I learn something new every time I attend.”
                                                            ~ Head, Smart Devices, Genentech

Event Summary

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.

Featuring In-depth Coverage On:

• Meeting Regulatory Standards in the Global Cleaning Validation Program
• Insights into Cleaning Deficiencies from FDA GMP Inspections 
• Automation of Cleaning Process Development 
• Leading Innovations in Cleaning Validation
• Case Study on the Global Implementation of a Risk-Based Contamination Control Strategy
• Case Study: A Risk-Based Approach to Material Transfer Validation
• Touching Base on Annex 1, Disinfection, Contamination Control, and Environmental Monitoring 
• Introduction and Overview of ASTM Cleaning Standards 
• Quantitative Measurement of Risk in the Cleaning of Pharmaceuticals & Medical Devices
• A Lean Approach to Analytical Methods to Support Cleaning Validation
• Creeping Residue on Medical Devices and Pharmaceutical Contact Surfaces—Managing the Unknown
• Hygienic Design Excellence for Enhanced Cleaning Validation
• Maintaining Your CV Program Across Your Processes
• And More!

Pharma Ed’s Cleaning Validation Summit 2025 is Sponsored by

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