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...






