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Statistical Concepts of Process Validation - Webinar By GlobalCompliancePanel

4 August 2011, Wilmington,DE, United States


Introduction
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".
Venue
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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