Managing clinical research is expensive and time consuming. And there’s never been an efficient way to unify the volumes of information you must handle throughout a clinical trial. Until now. MasterControl’s holistic clinical software eases the traditional burdens involved in clinical research. The comprehensive solution is designed to increase efficiency and the reuse of information. It’s the ideal platform for streamlining clinical operations and quality teams’ processes and tasks.
Each contract research organization (CRO), site and vendor has unique processes. But when it comes to quality, everybody needs to be on the same page. MasterControl unifies clinical operations and quality event management across all research activities. Plus, the system ensures that clinical and quality data from all sources always stays connected and audit ready.
Since our software is based on the TMF Reference Model, you can be assured of maximum efficiency and a centralized storehouse for all required TMF documents. The system allows you to view all TMF activities in real time. Download the complimentary TMF checklist template to see how the MasterControl configuration streamlines the collection and management of TMF documents.
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