Webinar: BREXIT: New UK Guidelines Explained

44 min

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 1^st 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