In vitro diagnostic medical devices

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Tuairim ó CESE: In vitro diagnostic medical devices

Background

The Commission proposal amends Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro diagnostic medical devices and deferred application of requirements for in-house devices.

In its, opinion, the Committee supports the Commission proposals which in the Committee's view are appropriate and necessary measures to ensure a high level of protection of health and the economic interest of this sector.

Practical information

Composition of the study group

Administrator in charge: Luis LOBO
Assistant: Catia ZIZZI

For more information please contact the INT Section Secretariat.