VEEVA DEVELOPMENT CLOUD
Operating System for
Product Development
Eliminate data and process silos across
clinical, quality, regulatory, and safety.
Veeva Development Cloud
Veeva Development Cloud is an operating system for product development that brings together applications for clinical, quality, regulatory, and safety to help organizations drive end-to-end business processes.
Today, product development and manufacturing systems are not well integrated, which creates inefficiencies and slows down critical operations. Veeva is the first and only company to offer unified suites of applications that are connected on a single cloud platform. This enables organizations to centralize content and data across global departments for greater efficiency and compliance. To learn more visit Veeva Vault Platform.
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.
improve visibility and oversight, and run faster, more cost-effective research programs.”
more effective and quicker to market.”
Vault Connections
Vault Connections are Veeva-delivered integrations that seamlessly transfer data and documents between clinical, quality, regulatory, safety, and commercial Vaults. They are designed to streamline cross-functional business processes by breaking down silos, providing greater visibility, and automating manual tasks. For more information on Vault Connections, visit our Resource Hub.
Share product, study, and site data and documents.
Speed change control and variation management.
Get up-to-the-minute site enrollment information.
Shorten submission timelines.
Vault Clinical Operations
Vault Clinical Operations is the only suite of unified clinical operations applications on a single cloud platform, accelerating trial execution and delivering real-time visibility.
Now, companies can eliminate system silos, streamline end-to-end clinical trial processes, and improve collaboration for sponsors, CROs, and clinical research centers.
Accelerate time to site activation.
Enable active eTMF for real-time inspection readiness.
Enable proactive trial management.
Pay clinical research sites faster.
Streamline and automate training.
Automate information sharing in clinical trials.
Improve patient experience.
Vault Clinical Data Management
Accelerate study timelines with modern, innovative applications for clinical data. Vault Clinical Data Management Suite (Vault CDMS) and Veeva RTSM are redefining data management to help clinical teams manage today’s trials with agility and speed.
Collect, clean, and review study data.
Manage complete and concurrent study data.
Randomize subjects and manage trial product supply.
Capture data directly from clinical trial participants.
Vault Quality
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.
Simplify postmarket surveillance for medical devices.
Document control for all GxP documents.
Manage and execute paperless validation.
Deliver the right content to the shop floor.
Ensure compliance and role-based qualification.
Accredited GxP eLearning courses.
Optimize QC labs for batch release.
Vault RIM
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.
Automate publishing during submission development.
Speed submission development.
Archive published dossiers securely in the cloud.
Vault Safety
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.
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Resources for Veeva Development Cloud
How can Veeva Help Your Business?
