MedPass is the leading EU Medical Device CRO, Regulatory and Reimbursement Consultancy. Our mission is to assist our clients by providing high quality, expert clinical trial and consultancy services.


For over 25 years, MedPass has helped more than 1,500 companies, from start ups to multi-nationals. We employ highly skilled professional staff that is expert in their various areas of specialization from clinical trial execution and biostatistics to market access and reimbursement. Furthermore, we have gained experience across a broad range of therapeutic areas, medical device technologies, and all phases of medical device development from preclinical to the post marketing phase. We are particularly known for our strong contribution to companies developing emerging technologies.


MedPass is the only Medical Device CRO that is fully ISO 13485 and ISO 9001 compliant across all of our clinical services, from regulatory submissions, through clinical monitoring and site management, data management and bio statistical reports. We were also the first Authorized Representative to be ISO 13485 certified.


From definition of scope of work and budgeting through project completion, MedPass’ teams remain highly flexible to respond to clients’ needs whenever necessary, whatever the urgency.


MedPass runs an efficient operation, based on teamwork and continuing attention to detail, minimizing client costs and offering total accountability.


MedPass’ staff turnover is far below the rates of most CROs due to our focus on staff development and retention. This is highly appreciated by clients, investigators and study personnel.