Product Development with
Latest Vault Innovations
New capabilities drive efficiencies across clinical,
quality, and regulatory.
Veeva Vault Development Cloud
Vault Development Cloud brings together applications for clinical, regulatory, and quality to help organizations eliminate silos and drive end-to-end business processes across product development.
Today, product development applications are siloed and not well integrated. Multiple systems create inefficiencies and slow down critical business processes. Veeva is the first and only company to offer suites of unified applications on a single cloud platform across the entire product lifecycle.
With all applications on the Veeva Vault Platform, companies can streamline product development information across regions and departments for greater efficiency and compliance.
- Faster time-to-market: Increase operational efficiencies by driving consistent, end-to-end product development business processes on a single system.
- Global alignment: Gain visibility across headquarters, sites, and countries.
- Comprehensive compliance: Achieve reliable information quality across the development lifecycle.
Veeva Vault Clinical suite is the industry’s first and only cloud platform that combines EDC, eSource, CTMS, eTMF, and study start-up to unify clinical data management and operations.
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.
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 2018.
Vault CTMS makes it easy for life sciences companies to unify clinical operations and processes, streamline trial management, and gain complete visibility across the trial portfolio.
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 automating country-specific processes.
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.
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 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.