---
title: 7 QMS Tools to Exhibit 21 CFR Part 820 Compliance for Medical Devices
description: Manufacturers can use their QMS to demonstrate FDA compliance with 21 CFR Part 820 regulations and focus on 7 specific capabilities within their QMS including risk management for medical devices to get the job done.
image: https://blog.etq.com/hubfs/7%20QMS%20Tools%20to%20Demonstrate%20Compliance%20with%2021%20CFR%20Part%20820%20for%20Medical%20Devices.jpg
---

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