CMC Medical Devices

CMC Medical Devices is a global regulatory consulting firm based in Malaga, Spain, specializing in market access and compliance for medical devices and in vitro diagnostic devices (IVDs).

We support manufacturers navigating complex international regulatory frameworks across Europe, the UK, Switzerland, the US, Australia, and key markets in South America and the Middle East. Our mission is to simplify global market entry for medical device companies by providing efficient, expert, and customized regulatory solutions.

CMC Medical Devices, now part of Registrar Corp, combines regulatory expertise, international representation, and advanced compliance infrastructure to support manufacturers worldwide. We offer a comprehensive suite of services including EU Authorized Representative (EU REP), UK Responsible Person (UK RP), Swiss Authorised Representative (CH REP), FDA Agent services, and more, ensuring your products meet the highest standards and achieve successful market authorization.

As a member of the Association of Authorised Representatives (EAAR & UKRPA), we’re dedicated to becoming the most reliable leading consultancy service provider for medical devices in the international market.