Introduction

The FDA QSR and the Medical Device Directive specify certain records that should be included in your organization's quality system - Design History File (DHF), Device Master Record (DMR), Device History Record (DHR), and Technical File (TF).

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Venue

Online Training

Livermore Common, Online Training, California, Fremont, 94539, United States

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Organised by

GlobalCompliancePanel

Contact information

Mr John Robinson
Livermore Common | Fremont | CA | 94539, Fremont, 94539, United States of America
8004479407
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