The Euro­pean Com­mis­sion has restruc­tured and fur­ther devel­oped its web­site on the Med­ical Devices Reg­u­la­tion (EU) 2017/745 (MDR) and In Vit­ro Diag­nos­tic Med­ical Devices Reg­u­la­tion (EU) 2017/746 (IVDR). We strong­ly encour­age all affect­ed par­ties to book­mark the page and also use the option to sub­scribe for the cor­re­spond­ing newsletter.

The web­page of the Euro­pean Com­mis­sion can be accessed here.