Our qualified and highly motivated monitoring team ensures best compliance with protocol and regulatory requirements. Thus, only high quality data will be submitted in a timely fashion.
Our success is based on the direct and frequent communication with the sponsor and trial site, which is a prerequisite for optimal performance and study quality. Therefore, only experienced project managers will be in charge of your trial and will be available for you as the main contact person throughout the project. Our monitors/clinical research associates guarantee up-to-date knowledge of your trial status at each participating hospital. Our monitoring activities include: