Veeva Systems has unveiled Veeva eSource, a new application within its SiteVault platform designed to streamline clinical trial data flow. The application aims to significantly reduce manual processes and enhance data quality through a direct data capture mechanism that eliminates the need for paper records at research sites.
Key Technical Highlights:
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Digital Data Capture: By enabling direct digital entry, eSource facilitates a “paperless” environment, ensuring integrated data transparency across clinical sites.
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Seamless Integration: The application is built to work in tandem with SiteVault CTMS (launched in August 2025). This integration enables a “straight-through” data flow from the research site directly to the sponsor.
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Operational Efficiency: The solution is engineered to simplify and standardize clinical trial management, providing a more efficient experience for both site personnel and patients.
Availability and Outlook: Veeva expects eSource to be available for early adopters in the second half of 2026. This launch follows Veeva’s strategic move to offer the SiteVault suite free of charge to a majority of research sites, further advancing the company’s vision of a connected and efficient clinical development cloud.