Veeva Systems has announced the launch of Veeva eSource, a new application within its SiteVault platform aimed at eliminating paper-based processes and streamlining clinical trial data flow at research sites. The solution is designed to reduce manual work, improve data quality, and accelerate the movement of clinical data from sites to sponsors.

Veeva eSource enables direct digital data capture at the site, integrates with electronic health records (EHRs), and supports automated data transfer into electronic data capture (EDC) systems. By removing duplicate data entry and enabling bidirectional integration between eSource and EDC, the application reduces errors, minimizes quality control workload, and eliminates the need for traditional source data verification. The result is a more efficient clinical trial process that allows site staff and sponsors to focus more on patients and study execution.

The new application is part of the Veeva SiteVault platform and requires SiteVault CTMS for use. Veeva plans to make eSource available to early adopters in the second half of 2026, positioning it as a key step toward fully connected, straight-through clinical data flow across the trial ecosystem.

Source: PR Newswire