Overview Of Central eSource From CRIO

Central eSource transforms the conduct of clinical trials by replacing disparate, site-specific source templates with a unified, sponsor-designed framework. By deploying a single, centrally managed template, trials launch more swiftly and collect standardized, high-quality data across all locations. Key safety and endpoint fields are uniformly captured, while eSource variables are seamlessly mapped to the EDC system. Sponsors and CROs gain immediate, secure, remote visibility into source records, reducing manual tasks and minimizing data-entry errors. In practice, CRIO’s Central eSource has driven improvement in enrollment rates and monitoring efficiency, and a reduction in protocol deviations to deliver faster, more reliable trial outcomes with far less site burden.