Guidance on significant changes regarding the transitional provision under Article 110(3) of the IVDR

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

In Vitro Diagnostic Medical Devices (IVD)

Published

May 1, 2022

Last updated

May 1, 2022

Description

Guidance on significant changes to transitional provision under Article 110(3) of IVDR for In Vitro Diagnostic medical devices (IVD).

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

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