Updates to the Human Factors Usability Engineering Guidance
Following the end of the transition period with the EU, the MHRA has just updated the Human Factors and Usability Engineering guidance (first published September 2017) document to reflect changes to the regulation of medical devices in the UK.
This guidance is specific to medical devices placed on the market in Great Britain (England, Wales and Scotland). For Northern Ireland, different rules apply to those in Great Britain.
It is intended for all classes of devices including drug-device combination products.
Download the full MHRA document here
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