Process Validation (aka Process Consistency)
Process Validation (aka Process Consistency)
Date: Tuesday, July 21, 2026
Time: 1:00 pm – 2:00 pm EDT
Fee: $295 Members / $395 Non Members
This session will detail the requirements for “Process Consistency” for low-risk drugs versus “Process Validation” for higher risk drugs.
This session will help you:
Understand what process consistency means.
Understand any international implications.
Learn some statistical tools you can use to demonstrate process consistency.
A short quiz will be administered at the end of the session. Participation in the quiz—and eligibility to receive a training certificate upon successful completion—is limited to individuals who have registered electronically through the LogMeIn© GoTo Training program.
Presenter
Richard Parcels
Richard Parcels is the Assistant Director, Regulation & Market Access for Cosmetics Alliance Canada. He works to enhance and protect the ability of member companies to conduct business effectively in Canada by fostering industry and government cooperation and by using sound science and risk-based approaches to inform and shape regulation, policy and guidance.
Richard has over twenty years of experience in the pharmaceutical, natural health product, cosmetic and medical device fields. He obtained a B.Sc. in Microbiology from the University of Guelph and has previously worked at Agriculture Canada, Warner-Lambert Parke-Davis, AstraZeneca, Estee Lauder and as an industry consultant for 12 years. He specializes in regulatory affairs, quality systems, training and auditing.
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