Medical device actors can gives their views and contribute to the future UK´s regulatory framework.
Since September 16, 2021, the Medical and Healthcare products Regulatory Agency (MHRA) gives the opportunity to manufacturers, researchers, suppliers, users, to express their views on how medical devices will be regulated across the UK (England, Wales and Scotland) in the future. Given that the EU MDR and IVDR apply for member states only, the UK is indeed seeking to create its own set of regulations.
In this article (UDI Compliance during Brexit) we summarized the main impacts the Brexit has so far on the sell of medical devices, as well as the new requirements.
Click here to go to the consultation questions: https://www.surveys.mhra.gov.uk/613cff3142a2b02700706bad
You can participate until November 25, 2021, 11.45pm (BST).
Note that a MHRA webinar about this consultation will be held online on October 5, 2021. As the registrations are sold out, you can sign up for the waiting list here.