EUROMED Authorized Services Kft, established in 2025, provides specialized regulatory, compliance, and authorized representative services for the medical devices sector within the European Union.
We support manufacturers, importers, and distributors in understanding and fulfilling their obligations under EU medical device regulations, including MDR requirements, regulatory documentation support, and compliance guidance.
Our services are delivered with a strong commitment to professionalism, confidentiality, and full respect of European legislation.
Our goal is to be a reliable partner for companies seeking clear, efficient, and compliant access to the European medical devices market.