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 their end-to-end clinical processes.
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.
Veeva is transforming how the life sciences industry captures and uses clinical data with Veeva Vault EDC and Veeva Vault eSource, the first applications for clinical data management on a single cloud platform.
Veeva is delivering a better EDC that lets you run the trial you want. Veeva Vault EDC enables complex multi-arm adaptive trials and allows mid-study design amendments without downtime. It is modern, adaptive, and fast – dramatically reducing trial cost and complexity.
Veeva Vault eSource provides a mobile application that enables investigational sites to enter patient clinical data directly into an electronic application, removing paper from the current standard EDC model. Vault eSource transforms site data collection and management for immediate data quality, eliminating wasted time and cost. Vault eSource is planned for availability in December 2017.
Veeva Vault Clinical suite is the industry’s first and only cloud platform that combines EDC, eSource, CTMS, eTMF, and Study Startup to unify clinical data management and operations.
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 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.
Veeva Vault RIM transforms regulatory efficiency with a unified RIM suite, providing a single authoritative source for submission documents, published dossiers, health authority interactions, and product registrations.
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.
Veeva Vault Submissions Publishing is an integrated publishing solution that dramatically speeds submission delivery. Use a continuous publishing process to create, validate, and submit eCTD dossiers.
Vault Submissions Archive keeps your complete history of submissions and health authority correspondence secure and easily accessible, supporting more timely and accurate responses to health authorities globally.
Seamlessly manage your quality processes and content with the Vault Quality suite of applications. All parties – life sciences companies, contract manufacturers, and suppliers – have access to a single authoritative source, enabling greater visibility and control.
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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