Despite the clarifications surrounding the definition of a medical device under the forthcoming EU Medical Device Regulation and the elaborated procedure on borderline decisions that is to come, complex qualification questions are likely to persist when these new rules come into effect.
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?