Spain | EU REP

Your Authorized Representative in Europe

We act as your Authorized Representative in the EU, ensuring that your medical devices comply with all European regulations, facilitating smooth and efficient market entry.

As the main headquarters of CMC MEDICAL CONSULTING GROUP, CMC DEVICES & DRUGS SL acts as an “Authorized Representative” for manufacturers without a registered office in the European Community, fulfilling specific obligations under relevant EU legislation.

CMC Medical Devices & Drugs S.L., a member of the EU Authorized Representatives Association (EAAR), is qualified and serves as one of the EU’s authorized representative companies with a broad global client base.

We can also serve as your legal representative in the EU for clinical trials of medical devices and/or In Vitro Diagnostic Devices.

Product Registration

Our service includes the registration of medical devices and/or in vitro diagnostic products with the competent authorities in Spain (AEMPS) before placing them on the market.

Once the registration is completed, manufacturers can export their products to the EU market.