The US Food and Drug Administration is updating for the first time in nearly seven years its guidance on how medical device manufacturers can use national and international voluntary consensus standards in their applications for market approval1,2.
The FDA has issued a draft guidance document to help device manufacturers and agency reviewers understand how they can use...
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?