Post Marketing Surveillance & Registry

Post marketing surveillance studies are becoming more and more frequentand increasingly larger in volume for medical devices.They do however necessitate a different approach in logistics and setup as well as ongoing efforts on data collection.

D-TARGET recognizes the importance to tailor activities like monitoring, project management, safety reporting and biometrics to the actual needs of PMS and registry type trials. We account for this by offering our tailored Express service, maximising study goals with cost efficient solutions, adapted to consider your local capabilities and ressources.

D-TARGET also supports you with accurate clinical planning; so as to allow clinical investigations from the pre-registration phase to flow naturally into an ongoing post marketing surveillance phase, taking into account the different needs for each phase of your clinical project.