What are our Representation Services?
For Non-European Medical Device industry, Med-Di-Dia will act as your company's EU Authorised Representative [E.A.R/ EU AR] and help place your Medical Device on the EU Market.
For European Companies, Med-Di-Dia will act as your Person Responsible for Regulatory Compliance [PRRC]. Through this, our experts will help you comply with all MDR/IVDR requirements.
For our clients in the Cosmetics Industry, Med-Di-Dia will act as a 'Responsible Person' and ensure your cosmetics are represented to the European Commission and can be sold on the EU Market.
Are you going for Clinical Trials? Med-Di-Dia will act as your Legal Rep. We will ensure that your clinical trials are represented and being complied with all regulatory requirements.