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CMC Medical Devices

Málaga, Spain · Business Services

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Last verified

May 2026

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.

Overview

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.
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Contact Details

+34951214054
contact@cmcmedicaldevices.com

Málaga, Spain, C/ Horacio Lengo

+5

Founded

2014

Company Type

Sole Proprietorship

Employees

10-20

Categories

Management Consulting
Strategic Planning
Business Consulting

Awards

2026 OpenSee all

Services

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UK Responsible Person (UK RP)
Business Consulting

Dedicated assistance with UK Responsible Person requirements, ensuring compliance with UK regulations for medical devices.

N/A

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