Introduction

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).

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Venue

OnlineTraining

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

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Organised by

GlobalCompliancePanel

Contact information

Dr webinars web
OnlineTraining, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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