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).
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0