The Reg­u­la­to­ry Affairs Net­work That Keeps Your Busi­ness Safe

mdi Europa spe­cial­izes on the ser­vices of an EU Autho­rized Rep­re­sen­ta­tive*, but we also pro­vide a world­wide net­work of high­ly expe­ri­enced con­sul­tants and experts on reg­u­la­to­ry affairs. Trans­la­tions, mar­ket research, mar­ket entry, tech­ni­cal file com­pi­la­tions etc., have been extreme­ly use­ful for our cus­tomers so far. 

If you like to find out more about our net­work of experts

We kind­ly rec­om­mend our page “Part­ners & Asso­ciates“.

* As defined in the Med­ical Devices Reg­u­la­tion (EU) 2017/745 (MDR), the In Vit­ro Diag­nos­tic Med­ical Devices Reg­u­la­tion (EU) 2017/746 (IVDR), the Active Implantable Med­ical Devices Direc­tive 90/385/EEC (AIMDD), the Med­ical Devices Direc­tive 93/42/EEC (MDD) and the In Vit­ro-Diag­nos­tic Med­ical Devices Direc­tive 98/79/EC (IVDD).