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.

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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