A modern content management system is crucial for life sciences companies working to keep pace with a rapidly changing industry. With Veeva's R&D solutions, you can manage content across your organization, partner ecosystem, and the globe — on a single cloud platform.
Each Vault application combines content, related information, and real-time reporting, equipping companies to complete processes faster and make teams more productive. During implementation we combine industry best-practices with your unique environment to drive efficiency into your operations.
- Global access: Easy, direct access for employees and trusted external parties. There's no need for VPNs or partner laptops.
- Greater visibility: Powerful reporting and dashboards provide insights that enable greater efficiency and better decision making.
- Control over document processes: Greater efficiency and compliance within your work streams.
Veeva’s suite of R&D applications is built on the Veeva Vault Platform. Native interoperability between Vaults enables content to flow across the enterprise. A single source of truth promotes consistency and efficiency while generating a complete chain of custody.
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 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.
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.