Features Briefs

Veeva Development Cloud Features Brief

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.