EU Authorized Representative Services
Consultancy, Reports, Analysis
Information
OMC Medical provides comprehensive EU Authorized Representative services to medical device manufacturers, ensuring compliance with EU MDR and IVDR regulations. By acting as your official representative within the European Union, OMC facilitates seamless communication with regulatory authorities, supports product registration, and ensures your technical documentation meets stringent EU standards. With expertise in regulatory compliance, OMC Medical helps manufacturers navigate complex requirements, maintain market access, and focus on innovation while ensuring patient safety and regulatory adherence.