Latest update: October 2022 


Regulation (EU) 2017/745 and Regulation (EU) 2017/746 This rolling plan contains a list of identified essential implementing acts and other relevant initiatives that the Commission has adopted or intends to adopt in the future. This plan is divided into two sections: implementing acts, and other actions/initiatives. This document is subject to quarterly review in order to provide national authorities and stakeholders with the most updated information. This document shall be read in conjunction with the “MDR/IVDR roadmap” adopted by the Competent Authorities for Medical Devices (CAMD) in cooperation with the Commission.