a TÜV Rheinland company
He 20 March 2023 is published on Regulation (UE) 2023/607 by which the Regulations (UE) 2017/745 y 2017/746, on medical devices and in vitro diagnostic medical devices.
With this new regulation, they look certification deadlines extended for our products. The new dates to take into account will vary depending on the type of product with which we work, and companies may benefit from them as long as certain conditions are met.
is eliminated, besides, the end date of commercialization of products in both regulations.
If you need more information regarding the news of the aforementioned regulation, do not hesitate to contact us.
