Common specification requirements for in vitro diagnostic devices

Information

Type

Closed consultation

Regulated products

IVDMD, Medical Devices

Topics

Health And Social Care

Published

May 21, 2024

Last updated

May 21, 2024

Description

MHRA seeks views on possible amendments to the Medical Devices Regulations 2002 to include common specification requirements for manufacturers of IVD devices.

Organization

Country / Region

United Kingdom

License

Open Government Licence 2.0 (United Kingdom)

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