Postponement of Medical Device Regulation: Survey; how do you use the 1 year more?

The Medical Device Regulation, MDR  (2017/745/EU) was supposed to come into force on 26 May 2020. It included some new, stricter requirements (e.g. . UDI, post market surveillance, new classification rules, etc.). A lot of Medical Device companies have been working hard to implement these new requirements. Now, due to the Corona pandemic the EU has postponed the coming into force date to 26 May 2021. So, there is one more year for the implementation, also for Notified Bodies. What do you think about this extra time? What will be your benefit of the postponement. Where are still problems you want to solve? Questions for which we would be interested in getting answers from your side. For that purpose we set up a brief survey. It has only seven questions and will thus only take you about five minutes - and your feedback will of course be anonymous. You will read about the results in one of the next newsletters. And if you do not already receive this newsletter on a regular basis, you can sign up for it free of charge.

Go back


Stay informed with the GMP Newsletters from ECA

GMP Newsletter

The ECA offers various free of charge GMP newsletters for which you can subscribe to according to your needs.

To subscribe, please click here.