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).