Medical Devices Regulation 2020
HOW TO PREPARE FOR THE KEY REGULATORY CHANGES AND THEIR IMPACTS.
Big change is coming to the medical devices industry. In 2017, the European Union approved the Medical Device Regulation (MDR). This new regulation will dramatically increase the safety requirements of both new and current medical devices.
These changes are now just around the corner – and will come into effect in May 2021. They will introduce significant alterations that are mandatory for medical device companies to comply with. Devices can no longer be delivered to the European market without conforming to the strict safety requirements of these new regulations.
This free white paper will help medical device companies prepare for these changes.
- The main changes introduced by the new MDR.
- The impact the MDR will have on key stakeholders.
- The best practices to allow companies to comply in a pain-free way.