Webinar: BREXIT: New UK Guidelines Explained
Recently the UK published its guidelines for the post-Brexit era, giving a NEW outlook of the long awaited UK regulations to be applied to medical device manufacturers wishing to place their medical devices on the UK Market after January 1st 2021.
In this webinar we provide an overview on:
- The UKCA Mark
- The expected UK requirements
- The differences between the UK and Northern Ireland
- The tasks and responsibilities of the UK Responsible Person