CMC Consulting Group is an international consulting firm specializing in regulatory affairs for medical devices. Founded in 2014 and headquartered in Spain, the company operates globally with offices in the United Kingdom, Switzerland, China, Australia, and the USA. Their services include guiding clients through the process of obtaining CE marking for medical and in vitro diagnostic devices under the new regulations (MDR 2017), as well as providing Free Sale Certificates and acting as Authorized Representatives in various markets. They also assist in compliance with regulations in the EU, UK, Switzerland, China, Australia, and the USA, enabling smooth market entry for medical devices. The company caters to manufacturers worldwide and offers personalized services tailored to their specific needs. Its expertise extends to areas such as ISO13485, EUDAMED Registration, Cosmetics, Personal Protective Equipment (PPE), and acting as a Legal Representative in Clinical Trials. With a focus on the Manufacturing and Medical Devices industries, CMC Consulting Group is positioned to provide essential support to companies navigating the complex landscape of global medical device regulations.
There is no investment information