Increase efficiency by standardizing regulatory documents and processes
Streamline reviews and approvals to speed study activation and enroll patients sooner
Gain real-time visibility into document status to improve compliance and oversight
Choose the Veeva SiteVault product that is right for you.
Veeva SiteVault reduces the administrative burden in clinical trials by simplifying the management of regulatory documents and processes across all studies to speed study execution. SiteVault can be used for all trials regardless of what technology sponsors are using, as well as the site file for investigator initiated trials.
Explore the features below and select the SiteVault product that is right for you.
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Veeva is the leading provider of clinical operations technology to more than 200 sponsors and leading research organizations.