The European Commission is proposing introducing extended transition periods for legacy devices that fall under the scope of the Medical Device Regulation (MDR) and lengthening the transition period during which these legacy devices can be placed on the market.
This article explains how the MDR clauses will be changed. The sector has no time to lose until the end of the one-week consultation period on the proposed amendments....
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?