Standardize and Accelerate Clinical Trials

Unify clinical systems and processes for efficient trials

Bring agility and speed to trials

Veeva Clinical Operations unifies systems and streamlines processes on a single platform, with a common data architecture, enabling end-to-end trial management to drive innovation and get devices and diagnostics to patients faster.

The Veeva Clinical Platform accelerates clinical operations and data management with a single source of information and collaboration to get products to patients faster. With dedicated applications for managing and tracking all clinical activities, including study documents, sponsors, site payments, and more, the Veeva Clinical Platform standardizes the entire clinical research management process in one centralized place.

  • Speed Study Timelines

    Enable technology-driven process improvements throughout trials from database builds to monitoring.
  • Drive Inspection Readiness

    Manage data in real-time for better decision-making and visibility into trial status and reporting.
  • Improve Trial Performance

    One source of truth for shared TMF, CTMS, site management, and RTSM with connected solutions.
  • Streamline Trials

    Streamline processes and improve how sponsors, CROs, and sites collaborate throughout the clinical trial process.

40%

decrease in TMF reconciliation time with Veeva eTMF

90%

reduction in monitoring visit preparation time

40%

faster study startup