Stay Organized and Compliant, Without the Effort

Standardize regulatory processes across all studies with a free, 21 CFR Part 11 compliant application.

Veeva SiteVault

SiteVault eReg is a free, easy-to-use application that liberates site staff from administrative burden so they can focus their time on what matters most.

Simplify regulatory processes and provide investigators, staff, and monitors secure access to study information. Documents received by sponsors through Study Connect are auto-filed to your regulatory binder to save time and improve compliance.

SiteVault is fully validated by Veeva and supports compliance with 21 CFR Part 11 and HIPAA.

No Cost

Start risk-free with a no-cost solution that is trusted by sponsors and fully validated. Expand capabilities over time as your needs evolve.

Starting is Easy

SiteVault is easy to set up and learn. Get comprehensive support, self-serve resources, and training designed for your busy schedule. There is no download or installation required.

Standardize Across All Studies

SiteVault can be used on any study, regardless of the sponsor. And sites can standardize their operations across studies and sites to reduce training burden and simplify document sharing.


Electronic Investigator Site File (eISF)

SiteVault provides an efficient way for investigators and site staff to maintain and access their regulatory and source documents electronically, in accordance with ICH-GCP and industry regulations.


Speed the signing process and eliminate the need to print physical copies by allowing investigators and staff to electronically sign documents from any location.

Remote Monitoring

Save time by providing monitors with secure, direct access to review regulatory and source documents to assist with source data review (SDR) and source data verification (SDV).

Digital Delegation

Get more done with an intelligent system that auto-populates the delegation log while you work. Gain visibility into staff qualifications and assignments and ensure compliance with system checks that help identify errors for you.

Central Documents

Store central documents (e.g. licenses, certifications, CVs) in a single location and automatically update them across relevant studies.

Easily Exchange Information with Sponsors

Seamlessly exchange documents and information with sponsors and CROs using Veeva Clinical applications via Study Connect.

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Reports and Dashboards

Gain real-time visibility across studies with configurable reports and dashboards. See staff workload, signature turnaround times and delays, monitoring history, training assignments and status, and more.


Complete document tasks right in the system with workflows to manage training, monitoring approvals, and signatures


Deliver a better patient experience while creating efficiencies for your site. Veeva eConsent may be provided by your sponsor for a study or enabled within SiteVault as a paid add-on to use across all studies.

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Enterprise Options

Upgrade to get access to Single Sign-on, API support, dedicated enterprise-level customer support, and more customization options.

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Frequently Asked Questions

What are Veeva's certifications and policies related to information security and data privacy?

Visit our Information Security and Data Privacy page to learn how Veeva and SiteVault help research sites comply with data privacy and other regulations.

Is there a limit for the number of studies, documents, or users that can be managed in SiteVault eReg?

There is no limit on the number of studies, documents, or users that you can have in Veeva SiteVault.

How long can documents be stored in SiteVault?

Study documents can be stored for 25 years following the date of study creation. Sites with enterprise features enabled can retain study data indefinitely or as long as they own the application.

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