After nearly four years spent retooling its Quality System Regulation – 21 CFR, Part 820 – the US Food and Drug Administration on 22 February finally released its draft rule that harmonizes the QSR with ISO 13485:2016.
BREAKING: FDA Releases ‘Quality System Regulation Amendments’ Draft Rule
After nearly four years of work, the US FDA has issued its new draft rule, “Medical Devices; Quality System Regulation Amendments.” If finalized, the QSR reg will be renamed the “Quality Management System Regulation,” or QMSR.

More from Regulation
More from Policy & Regulation
A concealed blunt-tip needle that can be inserted into the heart's pericardial space to treat cardiac arrhythmias has received FDA clearance, providing an alternative to catheter-based methods.
Biomedical Alliance’s Tom Melvin is on a mission to assist the European Commission comprehend the clinical gaps during its ‘targeted evaluation’ of the EU's medtech regulations and the pivotal role the EMA could play.
The FDA staff cuts will probably mean longer device review times at least in the short term, speakers said at a recent webinar. But innovations like AI and third-party review could offer some hope, even as tariffs create a new set of problems.