With over 35 years of experience in the practical work of pre- and clinical studies, we offer effective and tailor-made strategies for medical devices. Our expertise includes:
- Over 500 completed clinical trials
- 29 scientific conference contributions in the last 2 years
- 96% repeat orders from satisfied customers
Unlike classic pharmaceutical CROs, we specialise in medical devices and understand the specific regulatory requirements and processes.
Our digital processes optimise trial implementation and increase data quality. We use cutting-edge technologies that meet European, and moreover, German regulatory requirements . In doing so, we are regularly audited and certified. When it comes to risk management for your study, we don't leave anything to chance.
