Technology foundation for product development
Veeva Development Cloud is the technology foundation for product development that brings together applications for clinical, quality, regulatory, safety, and commercial to help organizations drive end-to-end 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 united 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.
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. View the Vault Connections Resource Hub for a full list of available Vault connections.
Veeva Clinical Operations
The only suite of unified clinical applicatipns on a single cloud platform.
The industry’s first and only suite of unified clinical applications–including study start-up, eTMF, CTMS, payments, and site connect on a single cloud platform–to accelrate trial execution and deliver real-time visibility.
Veeva Study Startup
Accelerate time to start activation.
Veeva CTMS
Enable proactive trial management.
Veeva eTMF
Enable active eTMF for real-time inspection readiness.
Veeva Payments
Pay clinical research sites faster.
Veeva Study Training
Streamline and automate training.
Veeva Site Connect
Automate information sharing.
Veeva Clinical Data
Accelerate study timelines with modern, innovative applications for clinical data.
Veeva Clinical Data helps clinical teams collect, aggregate, clean, and manage trial data with agility and speed.
Veeva EDC
Collect, clean, and review study data.
Veeva ePRO
Capture data directly from clinical trial participants.
Veeva RTSM
Randomize subjects and manage trial product supply.
Veeva eClinRO
Collect clinical measurements by healthcare professionals.
Veeva CDB
Manage complete and concurrent study data.
Veeva Quality Cloud
Modernize quality management while driving compliance and operational innovation.
Seamlessly manage your quality processes and content with Veeva Quality Cloud. All parties have access to a single authoritative source, enabling greater visibility and control.
Veeva QMS
Easily manage all quality processes.
Veeva Learn GxP
Accredited Gxp eLearning courses.
Veeva QualityDocs
Document control for all GxP documents.
Veeva LIMS
Accelerate batch release with a unified lab and quality ecosystem.
Veeva Training
Ensure compliance and role-based qualification.
Veeva Batch Release
Accelerate GMP release and market-ship decisions.
Veeva Validation Management
Execute paperless validation.
Veeva 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.
Veeva Registrations
Manage product registrations globally.
Veeva Submissions
Speed submission development.
Veeva Submissions Publishing
Automate publishing during submissions development.
Veeva Submissions Archive
Archive published dossiers securely in the cloud.
Veeva Safety
Veeva Safety is the only modern application for the collection, management, and real-time oversight of adverse events.
Veeva Safety
Real-time management and oversight for adverse events.
Veeva SafetyDocs
Centrally manage pharmacovigilance content.