FDA Adopts ISO Standard For Device Makers In New Rule
By Mark Payne ( January 31, 2024, 8:37 PM EST) -- The U.S. Food and Drug Administration has issued its final rule amending the good manufacturing practice requirements of the Quality System regulation to refer to an ISO standard that requires medical device makers to show they can meet customer and regulatory requirements....
Law360 is on it, so you are, too.
A Law360 subscription puts you at the center of fast-moving legal issues, trends and developments so you can act with speed and confidence. Over 200 articles are published daily across more than 60 topics, industries, practice areas and jurisdictions.
A Law360 subscription includes features such as
- Daily newsletters
- Expert analysis
- Mobile app
- Advanced search
- Judge information
- Real-time alerts
- 450K+ searchable archived articles
And more!
Experience Law360 today with a free 7-day trial.