Guidance on applying human factors to medical devices
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Health And Social Care
Published
September 19, 2017
Last updated
February 12, 2021
Description
MHRA has published guidance on the importance of applying human factors to medical devices, so they are designed and optimised to minimise patient and user safety risks.
Tags
Organization
Country / Region
United Kingdom
License
Open Government Licence 2.0 (United Kingdom)