This webinar presented by Vincent Rietsch (BU Manager, Medical Device Testing) covers a critical aspect of medical device manufacturing: How clean is your medical device after the manufacturing process?
Residuals like oils, particulates, and microorganisms can pose serious risks to patients. That’s why effective cleaning processes - and their validation - are essential.This session presents regulatory background, procedure for cleaning validation, test methods, parameters, and acceptance criteria.
Learn how to validate your cleaning process and meet safety and compliance standards.
English and french session available.