All your post-market surveliance at one place

Ranging from literature monitoring and individual case safety reports to aggregate data reports, we will help you to ensure compliance with MDR 2017/745.

Efficient and streamlined process

Data collection

Efficiently monitor all the phases of the lifecycle of your devices with real world data and evidence. Connect with health care professionals and evaluate their input.

Development as a continuous process

Our team will help you in the detection process of key trends important for your medical device development. Facilitate your decision making and subsequently device development with high quality data.

Connect and share

Access your data anytime anywhere with our share-point service. Stay on the safe side with data storage.