The European Academy of Paediatrics (EAP), along with 22 clinical associations, are calling on the European Commission to take urgent policy actions to prevent the loss of medical devices used in pediatric or orphan disease patients caused by medtech regulatory pressures in the region.
The implementation of the Medical Device Regulation has “unintentionally resulted in increased time and costs for manufacturers,” the clinical associations...
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?