Since the European Medical Device Regulation (EU MDR) was first announced in 2017, it has undergone several delays. In March 2023, the latest extensions were announced.
While further extensions are always possible, the updated implementation dates are now realistic. Don’t let past delays reduce today’s urgency. The EU MDR is already impacting both companies and patients, with some medical devices already being removed from the market, awaiting certification.
So as a medical device manufacturer, what do you need to know to avoid potential bottlenecks and profit-stopping issues?
Read this eBook to learn:
- Important dates and deadlines based on device classification
- Specific actions to take to prepare for certification
- Potential business and financial implications
- Considerations for future clinical research