Regulatory Documents Explained - DHF, DMR, DHR and TF
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- เผยแพร่เมื่อ 12 ก.ค. 2016
- 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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