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).
DHF, DMR, DHR and TF - Regulatory Documents Explained - Webinar By GlobalCompliancePanel
11 April 2013, Fremont, United States
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Livermore Common, Online Training, California, Fremont, 94539, United States
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