The FDA QSR requires device manufacturers to validate processes when the manufacturer cannot "fully verify the output". The manufacturer must validate these processes with a "high degree of assurance".
Statistical Concepts of Process Validation - Webinar By GlobalCompliancePanel
4 August 2011, Wilmington,DE, United States
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online training webinar
online training webinar, 1000 N West Street, Suite 1200, Wilmington,DE, 19801, United States
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globalcompliancepanel
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Mr webinar web
1000 N West Street, Suite 1200, 1000 N West Street Suite,, Wilmington, United States of America
8004479407
Contact us by email
1000 N West Street, Suite 1200, 1000 N West Street Suite,, Wilmington, United States of America
8004479407
Contact us by email
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