This white paper was updated July 2020 to reflect the one-year extension to the Date of Application (DoA) for the European Union’s Medical Device Regulation (EU MDR), due to the COVID-19 pandemic.
Many medical device manufacturers are fully immersed in the transition to MDR, but with lingering MDD certifications expiring in 2024, it’s time for anyone who has put it on the back burner to engage in the process in earnest.
Manufacturers with medical devices of all classes can benefit from the information and strategies outlined in this paper. Fill out the form to download your copy today.
©2024 RQM+ All Rights Reserved | Cookies Policy | Privacy Statement