CenTrial provides data management with paper CRF as well as Internet-based data input (eCRF) for EDC studies using validated data management systems in compliance with legal requirements (ICH-GCP, 21 CFR Part 11). By means of plausibility checks and query-management during the trial the data management ensures that relevant data are collected. Data management processes are quality-controlled and agreed upon with the client (data management plan). Our data management serve studies ranging from phase I trials with few paricipants to international, multi-centre studies with several thousand patients.
In compliance with your requests CenTrial provides full-service data management or takes over specific tasks, e.g. professional design and printing of paper-CRF.
Any questions, interested in our services? Contact us!
Tel.: +49 7071 9992-0