If you manufacture products outside the European Union and sell into the EU market, having a reliable EU Authorized Representative and EU Importer is not optional—it is a regulatory requirement.
CMS helps non-EU manufacturers seamlessly transfer their EU Authorized Representative and Importer while ensuring full compliance with EU MDR, IVDR, CE Marking, and EU product regulations.
Why Transfer Your EU Rep and Importer to CMS?
✔ Fast EU Authorized Representative transfer with minimal disruption
✔ Single, trusted EU Importer and Authorized Representative under one contract
✔ Full support for MDR, IVDR, medical devices, IVDs, and regulated products
✔ Expertise in CE marking, EU compliance, technical documentation, and vigilance
✔ Clear communication, transparent pricing, and responsive regulatory support
Whether you are facing non-responsive EU representatives, rising compliance costs, or preparing for MDR/IVDR audits, CMS provides a dependable solution for non-EU manufacturers entering or expanding in the European market.
Who We Support
- Non-EU medical device manufacturers
- Non-EU IVD manufacturers
- Companies needing an EU Authorized Representative
- Manufacturers seeking a compliant EU Importer
- Businesses requiring EU regulatory compliance services
Make the Switch with Confidence
Transferring your EU Authorized Representative and Importer to CMS is straightforward. Our regulatory specialists guide you through each step to ensure continuity, compliance, and peace of mind.
Contact CMS today to discuss your EU Authorized Representative transfer and learn how we can support your EU market access and CE compliance strategy.