Veeva Vault is a true cloud enterprise content management platform and suite of applications specifically built for life sciences.
Traditionally, companies have had to deploy applications for content and separate applications to manage associated data. Veeva Vault is the only content management platform with the unique capability to manage both content and data. Companies can now eliminate system, site, and country silos and streamline end-to-end processes across commercial, medical, clinical, regulatory, quality, and safety.
Because all Vault applications are built on the same core platform, companies gain additional efficiency and compliance through the streamlined flow of documents across regions and departments. Content stays accessible, current, and in context across the entire development and commercial lifecycle.
- Always current: Veeva is constantly innovating and delivering new IQ/OQ validated releases so you never get stuck on old software.
- High performance: Performance is continuously monitored and optimized to ensure everyone’s applications stay high performance.
- Zero footprint: No software to install, hardware to maintain, or costly upgrades.
- Serves companies large and small: Subscriptions scale up or down to fit any size business.
Accelerate study timelines with modern, innovative applications for clinical data.
Vault Clinical Data Management Suite (Vault CDMS) is redefining data management to help clinical teams manage today’s trials with agility and speed.
Collect, clean, and review study data.
Rapid coding for clinical terms.
Manage complete and concurrent study data.
The only suite of unified clinical operations applications on a single cloud platform.
The industry’s first and only suite of unified clinical operations applications—including CTMS, eTMF, and study start-up on a single cloud platform—to accelerate trial execution, and deliver real-time visibility.
Enable proactive trial management.
Enable active eTMF for real-time inspection readiness.
Automate information sharing in clinical trials.
Accelerate time to site activation.
Pay clinical research sites faster.
Modernize quality management while driving compliance and operational innovation.
Seamlessly manage your quality processes and content with the Vault Quality suite of applications. All parties have access to a single authoritative source, enabling greater visibility and control.
Easily manage all quality processes.
Deliver the right content to the shop floor.
Document control for all GxP documents.
Ensuring compliance and role-based qualifications.
Bring speed and agility to your regulatory team with unified RIM.
Manage the planning, execution, and oversight of all regulatory activities within a single, unified RIM platform.
Manage product registrations globally.
Speed submission development.
Automate publishing during submission development.
Archive published dossiers securely in the cloud.
Veeva Vault Safety is the only modern application for the intake, management, and real-time oversight of adverse events.
Real time management and oversight for adverse events.
Centrally manage pharmacovigilance content.
Manage signals from detection through risk evaluation and mitigation.
Provide a central hub for all of your medical content, from creation and approval, through to delivery – providing your customers the information they need, when they need it.
Speeds the creation, approval, and delivery of medical content.
Identify, profile, and engage all relevant healthcare decision makers.
Veeva Vault PromoMats combines digital asset management with review and distribution capabilities for end-to-end speed and compliance across your digital supply chain.
Commercial content and digital asset management solution.
Seamless multi-channel customer engagement across all channels.
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Demos & Videos
Single Source of Truth Across the Enterprise
How Veeva Vault facilitates information sharing across the value chain
What makes Veeva Vault unique in life sciences?