Central eSource revolutionizes clinical trials by offering a centralized template approach that significantly reduces site burden and improves data quality. Instead of sites creating their own complex source templates, a central template is developed by the sponsor and is then rolled out to sites participating in the trial. This process not only accelerates study startup and standardizes data collection, but also ensures consistent capture of key safety and endpoint data, pre-maps eSource variables to your EDC, and provides sponsors and CROs with real-time, remote access to source data across all sites. By reducing administrative work and preventing errors, CRIO Central eSource delivers 40% higher enrollment, 40% faster time to EDC entry, 20% fewer protocol deviations, and a 90% increase in monitoring productivity.
