In sum­mer 2019, mdi Europa has report­ed that the Euro­pean Com­mis­sion has restruc­tured its web­site on med­ical devices. Since then, man­u­fac­tur­ers could retrieve valu­able infor­ma­tion about EU reg­u­la­to­ry require­ments under the Med­ical Devices Direc­tive (MDD) and espe­cial­ly under the Med­ical Devices Reg­u­la­tion (MDR). 

The Com­mis­sion now pub­lished a notice on the web­site that the med­ical devices top­ic will be trans­ferred to anoth­er loca­tion under Direc­torate-Gen­er­al for Health and Food Safe­ty. New infor­ma­tion will thus be post­ed on anoth­er web­site sec­tion – view here.

Source: Euro­pean Commission

For fur­ther infor­ma­tion on this sub­ject, we rec­om­mend our fol­low­ing con­tent and articles