2017/745 extension: is it sufficient if manufacturers have already adopted all the strategies necessary to transition to the new regulation, or have they already begun the process of compliance with the new regulation?
On February 16, 2023, the European Parliament cast its favorable vote on the transitional provisions for medical devices and IVDs, as stated in the approved text, and available at the following link: https://www.europarl.europa.eu/plenary/en/infos-details.html?id=922&type=priorityInfo Despite the constant increase in the number of notified bodies designated in compliance with Regulation (EU) 2017/745, the overall capacity of the […]
