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.
Administrator in charge: Luis LOBO
Assistant: Catia ZIZZI
For more information please contact the INT Section Secretariat.