Medical Device Record Retention Procedure Template – QMSR Compatible

QMSR Compatible Record Retention Procedure Template

FDA requires medical device records to be retained for specific periods — and knowing what to keep, for how long, and in what format is critical. This Record Retention procedure template provides a comprehensive retention schedule and management framework compatible with QMSR (21 CFR Part 820).

What's Included

• Complete Record Retention procedure compatible with QMSR
• Record retention schedule by record type
• Physical and electronic record storage requirements
• Record destruction authorization process
• Editable in Microsoft Word and Google Docs

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