“The medical device regulation was intended to improve the safety and quality of medical devices and to bring a harmonized regulatory framework for medical devices across the EU,” starts a commenter on the European Commission’s rollout of the Medical Device Regulation.
“However, the implementation of the MDR has caused disruptions in the medical device industry, with some manufacturers raising prices or...
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Pink Sheet 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?