Notify MHRA about a clinical investigation for a medical device

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Health And Social Care

Published

December 18, 2014

Last updated

September 6, 2024

Description

Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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