Brexit Webinar: 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 covered:

  • The UKCA Mark
  • The expected UK requirements
  • The differences between the UK and Northern Ireland
  • The tasks and responsibilities of the UK Responsible Person

At the end of the webinar, we will also present a first look onto the UK RP services offered to medical device manufacturers by Obelis UK Ltd and as usual, we will make available special templates to support your compliance with the MDR.

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