Veeva SiteVault - One place to manage your studies and work with sponsors. Ditch the paper binders and enable monitoring in a compliant system. Expand your reach and make it easier for patients to participate in trials. Watch an end-to-end demo. Questions? Contact Us. Veeva R&D Summit returns this September to Boston!

Veeva SiteVault is an eRegulatory application that reduces administrative burden in clinical trials by replacing manual, paper-based processes and connecting you to more than 400 sponsors that use Veeva clinical applications.

SiteVault is used to exchange study information with sponsors and manage site regulatory binders or the Investigator Site File (ISF) across all types of clinical research, such as industry-sponsored, Federally funded and single-site Investigator Initiated Trials (IITs).

Watch a 2-minute overview of Veeva Site Connect here. how Veeva can help? Clinical research sites work in many systems to exchange trial information with sponsors. SiteVault provides one place for sites to work with sponsors and manage their studies.

Learn about using SiteVault and get up and running quickly. Learn how manage users and records as a SiteVault administrator. Manage the teams, vendors, and participants for your studies. Learn how to build your eBinder and upload and manage documents. Store and manage all of your documents.

Veeva SiteVault is a free eISF / eRegulatory application for research sites to enable remote monitoring and efficiently manage trial documentation across studies and sponsors. To learn more about Veeva SiteVault click here. how Veeva can help?

SiteVault is a powerful solution for managing all of your site’s documentation across all of your studies. In this one application, you can find the following features: Study eBinder to easily manage and track your study documentation progress; Veeva eConsent to electronically consent participants across some or all of your studies

PLEASANTON, CA — April 1, 2025 — Veeva Systems (NYSE: VEEV) today announced Veeva SiteVault CTMS, a clinical trial management system for research sites that is integrated with SiteVault eISF and SiteVault eConsent to allow sites to comprehensively manage clinical trials within one main system. Integration with sponsors using Veeva’s ...

Use your VeevaID as a single login to all your Veeva products for sites. Learn more. Manage study documents, monitoring, and patient consents across all your studies. Manage digital patient consent forms, both on-site and remotely, through SiteVault. Work with your sponsor/CRO to collect and manage patient data.

Veeva SiteVault is a single place for sites to manage their studies and exchange information across the hundreds of sponsors and CROs that already use Veeva to run their trials. Watch this 1:40 video to learn how SiteVault enables better, more efficient collaboration between your site and sponsors, and more time to focus on your patients.