IMed Consultancy

IMed Consultancy is a specialized regulatory and quality consultancy serving the medical device and in vitro diagnostic (IVD) industries. The company provides comprehensive support for global market access, including regulatory strategy, technical documentation, and Quality Management System (QMS) implementation. They offer specific services such as UK Responsible Person (UKRP) and European Authorized Representative (EAR) roles for international manufacturers. IMed also focuses on digital health and software as a medical device (SaMD), ensuring compliance with evolving regulations like the EU MDR and IVDR. The firm is headquartered in the UK and supports clients ranging from startups to established multinational corporations.