Veeva Systems announced Veeva eSource, a new Veeva SiteVault application designed to eliminate paper-based processes at clinical trial sites and significantly improve data quality through direct digital data capture, EHR integration, and automated data flow into EDC systems. The solution enables straight-through clinical data flow from site to sponsor by integrating electronic health records, providing a simple application for direct trial data capture, and automating bidirectional data exchange with EDC platforms using open APIs. “I’m excited to see Veeva eSource in action; although there are other options in use by sites, traditional eSource is still incredibly time-consuming to program, complete, and transfer data from eSource to EDC,” said Alisha Garibaldi, CEO, Skylight Health Research. “A seamless flow of data from Veeva eSource to EDC will reduce errors, minimize QC processing, and allow us to spend more time where it matters – with our patients.”
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By capturing source data directly, Veeva eSource also eliminates the need for labor-intensive source data verification. “For the first time, we are connecting data and processes to enable straight-through clinical data flow from site to sponsor,” said Jim Reilly, president of Veeva Development Cloud. “It is a major step toward our vision to simplify, standardize, and connect clinical trials for higher efficiency and a better experience for sponsors, sites, and patients.”