GovWire

Guidance: In-house manufacture of medical devices in Great Britain

Medicines Healthcare Products Regulatory Agency

December 16
11:44 2024

class="gem-c-govspeak govuk-govspeak gem-c-govspeak--direction-ltr govuk-!-margin-bottom-0">

The legal requirements healthcare establishments should comply with when manufacturing medical devices in-house.

Please note that this guidance is currently under review. The MHRA will publish updated guidance in due course. Health institutions may continue to follow the guidance linked above until further notice.

Updates to this page

Published 1 September 2014
Last updated 16 December 2024 +show all updates
  1. Amended to add note that guidance is currently under review.

  2. Updated as a result of the end of the Brexit transition period.

  3. First published.

Sign up for emails or print this page

Share This


Enjoyed this? Why not share it with others if you've found it useful by using one of the tools below: