SiteVault enables clinical research sites to save time and accelerate research by streamlining the management of regulatory documents and processes in a modern eRegulatory system.

Vault CTMS is the only modern cloud application that makes it easy for life sciences companies to unify clinical information and processes, streamline trial management, and gain complete visibility across the trial portfolio.

Vault EDC provides a fast and intuitive interface for capturing and reviewing clinical trial data. Designed for flexibility, Vault EDC allows you to run complex multi-arm adaptive trials and make mid-study amendments without downtime or migrations. Veeva is delivering a better EDC that lets you run the trial you want.

Designed specifically for the life sciences industry, Veeva Vault eTMF is the only application that enables active TMF management for real-time inspection readiness, visibility, and control. Seamless interoperability with CTMS and Study Start-up allows sponsors, CROs, and sites to access the same clinical information, streamlining collaboration and increasing efficiency.

Veeva Vault Study Startup speeds clinical trials by bringing together study start-up activities and processes in a single, easy-to-use application. Part of a unified suite of clinical operations applications, Vault Study Startup enables seamless sharing of information and documents across CTMS, eTMF, and study start-up processes, improving collaboration and increasing efficiency.

Medical device and diagnostic companies are struggling to keep up with changing regulations and the growing demand for clinical data is draining resources. Vault Medical Device Suite streamlines the device and diagnostic lifecycle for greater efficiency and compliance.