Looking for clinical data management solutions?
Veeva offers the industry’s first and only suite of unified clinical operations applications—including CTMS, eTMF, study start-up, and site document exchange on a single cloud platform—to accelerate trial execution, and deliver real-time visibility. Key to this first-ever unification of clinical operations systems is Veeva Vault Platform's unique ability to manage both content and data, eliminating systems silos, enabling true end-to-end clinical trial processes.
- Increased productivity: Reduce complexity, automate and streamline trial processes by allowing key stakeholders, both internal and external work in a single system.
- Full visibility: Improve decision-making based on an accurate, comprehensive view of study status across the entire operational team.
- Increased compliance: Gain complete oversight of the end-to-end clinical process with a single source for content and data through a streamlined and consistent user interface.
- Single cloud platform: For content and data applications, providing a single source of truth and enabling seamless end-to-end processes.
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 startup content and data, and incorporating country-specific intelligence in study start-up workflows.
Vault SiteExchange makes it easy for sponsors, CROs, and investigator sites to collaborate on study activities by providing a single point of access and consistent processes for document exchange during clinical trial execution.