IMed Consultancy
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"Regulatory and quality consultancy helping medical device and IVD companies navigate compliance"
Banbury
•11 - 50 Employees
•Consulting
About IMed Consultancy
IMed Consultancy provides regulatory and quality assurance expertise to medical device and IVD companies worldwide. The team guides manufacturers through CE marking, MDR and IVDR compliance, quality management systems, UK Responsible Person services and global registrations, supporting businesses from early design through market entry and ongoing compliance. Founded in 2012, the consultancy works as a flexible extension of client teams, combining industry experience with regulatory knowledge. Whether supporting an SME with its first device or managing complex international submissions, IMed delivers practical solutions that balance compliance with commercial realities, enabling safe, effective medical technologies to reach patients.
25
Team Members
2012
Founded
Consulting
Sector
Hybrid
Work Environment
Our Vision
A healthcare landscape where regulatory compliance enables rather than hinders the delivery of safe, innovative medical technologies to patients worldwide
Our Mission
At IMed Consultancy, our mission is to support medical device and IVD companies in navigating global regulatory environments through expert, flexible consultancy that prioritises client needs, timelines and budgets while ensuring patient safety