Veeva Vault Clinical Suite

Veeva Vault Clinical Suite the industry's first cloud platform that combines EDC and coding, data management, CTMS, eTMF and study start-up to deliver the most comprehensive suite of clinical cloud applications. For the first time, life sciences companies can unify clinical operations and data management on a single platform to create a single source of truth, streamline end-to-end processes, and help sponsors, CROs, and sites improve how they work together throughout the clinical trial process.

  • Single source of truth: Reduce complexity by managing clinical operations and data in a single system that automates and streamlines trial processes.
  • Complete visibility: Improve decision-making based on an accurate, real-time, and comprehensive view of study status.
  • Increased compliance: Gain complete oversight of the end-to-end clinical process, delivering real time actionable insights.
  • Unified and connected: A unified suite within Veeva Development Cloud, streamlining cross-functional business processes with a single cloud platform.
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Vault EDC accelerates study cycle times with faster builds, easy amendments, intuitive data capture, and next generation monitoring and data review.

Vault Coder provides an intuitive interface with innovations for fast and accurate coding of adverse events, medical histories, and medications using MedDRA and WHODrug dictionaries.

Vault Data Workbench provides a complete and concurrent view of all your study data for cleaning, reporting, and export. (Target availability in 2020.)

Vault CTMS unifies clinical information, documentation, and processes globally to reduce complexity, increase transparency, and speed time to critical decision making.

Vault eTMF enables active TMF management for real-time inspection readiness, visibility, and control.

Vault Study Startup accelerates time to site activation by bringing together start-up content and data, and incorporating country-specific intelligence in study start-up workflows.