EU Medical Device Regulation (MDR) has been postponed until 26 May 2021 due to current Corona situation!
The decision to postpone the date of application of MDR was published in the Official Journal today, 24 April. This means that manufacturers of medical devices intended for the European market are now allowed one more year of transition time to the new regulation.
If you need help interpreting what this means for you and your business, don’t hesitate to contact our team of experts at Devicia AB and our collaboration partners at Morris Law (Advokatfirman Morris AB) and Clarvin AB. We will offer a complimentary webinar on the topic shortly – stay tuned to our LinkedIn-pages for more information! Siri Mårtensson Hjälmberg, Karin Odkrans, Åsa Runnäs and Elisabeth Liljensten.