Overview: The FDA QSR and the Medical Device Directive specify certain documents or records that should be included in your organization's quality systems - Design History File (DHF), the Device Master Record (DMR) the Device History Record (DHR), and the Technical File (TF).
Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
14 February 2012, Wilmington, United States
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OnlineTraining
OnlineTraining, 1000 N West Street, DE, Suite 1200, Wilmington, 19801, United States
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OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
Contact us by email
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