Content management in the cloud – built for life sciences
Veeva Vault provides a content management platform and suite of applications built for life sciences. Each application includes rich functionality to meet the needs of a specific business process.
The native interoperability between Vault applications provides additional efficiency and compliance by streamlining the 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.
Vault CTMS unifies clinical information, documentation, and processes globally to reduce complexity, increase transparency, and speed time to market. Vault CTMS is planned for availability in the first quarter of 2017.
Vault eTMF enables active TMF management for real-time inspection readiness, visibility, and control.
Veeva Vault Study Startup accelerates time to site activation by bringing together startup content and data, and automating country-specific processes.
Vault Investigator Portal speeds the collection, sharing, and tracking of all trial-related content between sites and sponsors and CROs. A personalized homepage for each site displays clear and prioritized tasks, helping sites work smarter, not harder.
Vault Registrations provides a single global application for planning, managing, and tracking product registrations, and health authority correspondence and commitments. Vault Registrations also helps organizations prepare for IDMP compliance and message generation.
Vault Submissions unites contributors, partners, and affiliates in the cloud with a single destination for regulatory documents. Global and regional submission dossiers harmonize planning and provide real-time visibility into submission readiness.
Vault SubmissionsArchive keeps your complete history of submissions and health authority correspondence secure and easily accessible, supporting more timely and accurate responses to health authorities globally.
Vault QMS provides global management of quality processes – for all parties – enabling end-to-end control and visibility. Easily support proactive management initiatives and Deviation, Internal/External Audit, Complaint, Lab Investigation, Change Control, and CAPA processes, or configure your own.
Vault QualityDocs provides a single global source for all quality, manufacturing, validation, and other GxP documents. Vault’s state-of-the-art technology and UI improves adherence to—and reduces the burden of—GxP compliance.
Vault MedComms provides a user-friendly global repository that simplifies collaboration and version control when managing all types of medical affairs content. The integration with a case management tool provides call centers with direct accesses to the most current information.
Vault PromoMats gets your message to market faster with easy internal and external collaboration and more efficient reviews. The single-click distribution and withdrawal through multichannel Veeva CRM keeps content current and compliant.
Vault Platform is easily configured to build new applications. Manage any type of high-value information with custom applications that interoperate with your other Vaults. Your applications benefit from Veeva’s stream of innovation and your configurations stay current through every upgrade.
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