The Euro­pean Com­mis­sion is cur­rent­ly con­duct­ing a tar­get­ed eval­u­a­tion of Reg­u­la­tions (EU) 2017/745 on med­ical devices or 2017/746 on in vit­ro diag­nos­tic med­ical devices respec­tive­ly (MDR or IVDR). In this con­text, it launched a sur­vey to seek input from the mar­ket. This is a good chance for all par­ties involved to pro­vide feed­back. The sur­vey can be accessed here. It is open until March 21, 2025.

A sec­ond sur­vey was launched on behalf of the Euro­pean Com­mis­sion. The aim of this sur­vey is to “col­lect infor­ma­tion and data on the sta­tus of the imple­men­ta­tion of Reg­u­la­tion (EU) 2017/745 (MDR) and Reg­u­la­tion (EU) 2017/745 (IVDR).” It is already the sec­ond sur­vey in the frame­work of the “Study sup­port­ing the mon­i­tor­ing of the avail­abil­i­ty of med­ical devices on the EU mar­ket”. The sur­vey can be accessed here. 

Source: Euro­pean Commission

Accom­pa­ny­ing this sub­ject we rec­om­mend the fol­low­ing con­tent on our website