Veeva Systems has announced Veeva eSource, a new Veeva SiteVault application designed to streamline the flow of clinical trial data. More specifically, the application will “significantly” reduce manual clinical trial processes, and increase data quality.

In addition, Veeva eSource can eliminate paper at a particular site via a direct data capture application.

Veeva Officials React

Nick Frenzer, general manager of Veeva site solutions, touted the announcement.

“Veeva eSource advances our goal of delivering significant efficiency and simplicity for clinical trial sites,” Frenzer said. “By delivering eSource, we can complete the picture to provide integrated data transparency across a site to improve trials.”

Part of Veeva’s SiteVault platform, eSource requires SiteVault CTMS to simplify and streamline experiences for site and patient alike.

More on Clinical Trial Management

First announced in April 2025, SiteVault CTMS is a clinical trial management system for research sites. Integrated with other SiteVault properties, it allows sites to manage clinical trials comprehensively, within a main system.

Veeva first made SiteVault CTMS available in summer 2025—for free to sites with up to 20 concurrent active studies.

“High-quality cloud software and seamless sponsor integration will help sites be more efficient,” Frenzer said at the time. “By making the SiteVault suite free for over 90% of research sites, we are doing our part.”

A First for Veeva

Jim Reilly, President of Veeva Development Cloud, said Veeva eSource breaks new ground.

“We are connecting data and processes to enable straight-through clinical data flow from site to sponsor,” Reilly said. He added it encapsulates “our vision to simplify, standardize, and connect clinical trials for higher efficiency and a better experience.”

Veeva expects eSource to be available for early adapters sometime in the second half of 2026.