The US Food and Drug Administration says a draft rule that aims to replace its decades-old Quality System Regulation (QSR; 21 CFR, Part 820) with a new Quality Management System Regulation (QMSR) will help harmonize QMS requirements and get medical devices into the hands of patients more efficiently.
The agency released its long awaited draft reg, “Medical Devices; Quality System Regulation Amendments,” on 22 February, and published it in the Federal Register on 23 February
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Medtech Insight for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?