Medical Devices – Post-Brexit Regulatory Landscape in the UK
With the Brexit commencement, from Jan 1, 2021, there have been a lot of changes in the UK’s medical devices regulations, which the executive Regulatory Authority in the UK – MHRA has devised. Medical device manufacturers willing to enter the UK market especially, England, Scotland and Wales, will have to follow the applicable MHRA UK regulations.
While some changes have come into effect immediately, others have a grace period for compliance. What are those changes, and how are they affecting the medical device landscape in the UK? Let’s decode.