18 November 2020
Following our own well attended webinar with MHRA on 3rd November, which provided members with an overview of the incoming regulatory requirements for medical devices for the UK market from the beginning of next year, we had hoped to circulate the slides to members.
These slides have not been approved for release by the Department for Health and Social Care, however a previous webinar recording has now been made available.
The presentation covers the same material explored in our own webinar, and we have also submitted an extensive collection of members' questions to the MHRA for written responses, which will be shared as soon as they are available.
Watch the recording
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