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Clarifying Device History Record Issues | mddionline.com

According to 21 CFR 820.3(x), rework means action taken on a nonconforming product so that it will fulfill the specified device master record requirements ...

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查詢 「Device master record」的人也找了：

  1. DHF, DMR DHR
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  2. Device history Record
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  3. 21 CFR part 820.181 device master record DMR
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  4. Device History Record example
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  5. DMR FDA
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  6. Medical device file
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  7. Design History File
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