mdi Europa is proud to be part of the renowned reg­u­lan­et® net­work – a glob­al net­work of qual­i­fied inde­pen­dent con­sul­tan­cies with exper­tise in devel­op­ment, reg­u­la­to­ry, mar­ket access, and life­cy­cle management. 

As a reg­u­lan­et® part­ner, our clients ben­e­fit from a glob­al net­work of exper­tise cov­er­ing the reg­u­la­to­ry require­ments of the med­ical device indus­try in over 90 countries.

Our sta­tus as a reg­u­lan­et® part­ner enables us to pro­vide even more tar­get­ed sup­port – with a deep under­stand­ing of local and inter­na­tion­al reg­u­la­tions, whether it’s mar­ket access, reg­u­la­to­ry approvals or MDR and IVDR com­pli­ance.

By work­ing close­ly togeth­er in the reg­u­lan­et® net­work, we ensure that your prod­ucts reach the mar­ket safe­ly and com­pli­ant­ly – effi­cient­ly and with min­i­mal effort for you.

Con­tact us today to find out how mdi Europa can help your projects go global.

Accom­pa­ny­ing this sub­ject we rec­om­mend the fol­low­ing con­tent on our website