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Reusable Device Cleaning, Disinfection, and Sterilization Validations: Overview and Key Design Considerations for Device Engineers - Webinar By GlobalCompliancePanel

22 February 2012, Wilmington, United States


Introduction
Validation of reusable medical devices requires that the manufacturer develop methods for cleaning (after use) washing to remove all foreign matter possibly disinfecting and repackaging for the next use.
Venue
OnlineTraining

OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States

Organised by
GlobalCompliancePanel
Contact information
Mr webinars web
OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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