Can anyone kindly link to where there is some authoritative documentation on the current requirements for sale of medical devices in the UK post-brexit?
I've been searching on the UK.gov website for pages updated since October, but can't seem to find anything clearly laying out what's changed (if anything).
In fact, their Medical devices: conformity assessment and the CE mark page hasn't been updated since 2016!
Can I continue to market my CE-marked devices in the UK? ...or are there now some additional requirements/regulations?
I've been searching on the UK.gov website for pages updated since October, but can't seem to find anything clearly laying out what's changed (if anything).
In fact, their Medical devices: conformity assessment and the CE mark page hasn't been updated since 2016!
Can I continue to market my CE-marked devices in the UK? ...or are there now some additional requirements/regulations?