Get ready for the new EU Medical Device Regulation!
The new Medical Device Regulation (MDR) which becomes fully applicable on May 26, 2021 is initiated to improve patient safety, to increase transparency and traceability but also to bring EU legislation in line with technical advances and create a fair market access for manufacturers.
In the first session of this webinar series Dr Tina Amini, Medical Device Division Director at NDA presents an introduction to MDR and the key changes accompanied, such as the new rules, new device classifications and new roles required in an easy-to-follow way.
Fill out the form on the right to download this content.
Your drug development needs are unique
Contact us to learn how our experts can support you to meet all regulatory, quality and safety requirements and ensure the best path to approval.
Let's Bring Medicines to the World