The US Food and Drug Administration has announced a February webinar to discuss and answer stakeholder questions about two draft guidance documents the agency released this week related to the COVID-19 pandemic.
Published in the Federal Register on 23 December, the draft guidance “Transition Plan for Medical Devices Issued Emergency Use...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?