Guidance
In-house manufacture of medical devices in Great Britain
Guidance for healthcare establishments that manufacture medical devices in-house.
Documents
Details
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
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Amended to add note that guidance is currently under review.
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Updated as a result of the end of the Brexit transition period.
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First published.