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.
Reusable Device Cleaning, Disinfection, and Sterilization Validations: Overview and Key Design Considerations for Device Engineers - Webinar By GlobalCompliancePanel
22 February 2012, Wilmington, United States
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OnlineTraining
OnlineTraining, 1000 N West Street,, Delaware, Suite 1200, Wilmington, 19801, United States
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OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
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