The new regulations in force, in particular the MDR EU 2017/745 Regulation, are pushing manufacturers and institutions to reorganize the management of their clinical studies. 

GEPROMED offers services to design, set up and conduct clinical studies in accordance with the MDR EU 2017/745 Regulation. It ensures patient safety and the reliability of the clinical data collected. We support you whatever your therapeutic field, on the totality of your study or just a part, depending on your needs. The platform is certified ISO 9001.

Find here the panel of services offered by GEPROMED

GEPROMED has already successfully collaborated with more than twenty industrial and institutional sponsors in order to evaluate the safety and performance of medical devices before and after CE marking.  

GEPROMED has a multidisciplinary team: surgeons, pharmacists, project managers, engineers, clinical study technicians and clinical research associates, which makes it a key player to support you in your clinical studies on all types of medical devices. 

Our major asset is our close collaboration with the University Hospitals of Strasbourg, with our clinical study technicians integrated in the dedicated departments. 

Do not hesitate to contact us at: contact@gepromed.com, an expert will get back to you shortly.