Development Cloud Demo Center

From clinical trials to quality and manufacturing, Veeva’s cloud-based content management applications are developed specifically for the global life sciences industry. See how different content management in the cloud can be by taking a look at the sneak peeks below, then be sure to contact us for more information.
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VEEVA DEVELOPMENT CLOUD

Eliminate System, Site, and Country Silos
See how Veeva Development Cloud drives end-to-end business processes across clinical, regulatory, and quality for greater efficiency and compliance throughout the product lifecycle.

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Veeva Vault for Clinical Operations

Accelerate Trial Execution
Watch how Veeva Vault for Clinical Operations leverages the Vault platform to eliminate silos across CTMS, eTMF and study startup to streamline end-to-end clinical trial processes, accelerate trial execution, and deliver real-time visibility.

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Veeva Vault for Clinical Operations

Streamline End-to-End Clinical Trial Processes
Watch how Veeva Vault for Clinical Operations unifies the site initiation process and streamlines communications between start-up and site monitoring teams

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VEEVA VAULT CDMS

Vault CDMS QuickView Demo
Veeva's innovative interface for data review improves the speed and accuracy of SDV by displaying only the data that needs action or attention. Vault CDMS translates your risk-based monitoring strategy into a dynamic action plan that helps CRAs focus on what matters most.

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Veeva Vault CTMS

Enable Faster, Higher-Quality Trials
Take a peek at how Vault CTMS makes it easy for life sciences companies to unify clinical information, streamline processes, and gain complete visibility across the clinical trial portfolio.

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Veeva VAULT ETMF

Streamline Document Collection, Management, and Analysis
Take a quick look inside Vault eTMF to see how sponsors and CROs are able to easily manage their clinical trials, as well as create comprehensive business reports, by utilizing a modern, cloud-based electronic trial master file solution.

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Vault Study Startup Demo: Part 1 - Homepage

Improve Visibility of Study Start-up Progress
See how Vault Study Startup gives study start-up specialists and managers complete visibility into critical milestones, tasks, and activities with a dedicated homepage.

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Vault Study Startup Demo: Part 2 - Country Intelligence

Accelerate Global Site Activation
Learn how study start-up teams can easily navigate complex and frequently changing country-specific processes through pre-configured workflows in Vault Study Startup.

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Vault Study Startup Demo: Part 3 - Site Greenlight Process

Streamline and Standardize Site Greenlighting
Learn how Vault Study Startup makes it easy to efficiently manage the site greenlight process through visualization, collaborative review, and actionable insights.

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Veeva Vault QMS

Vault QMS Demo
See how Veeva Vault QMS easily manage all your quality processes in one place.

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Veeva Vault QualityDocs

Consistent Audit Trail, Pervasive Access, and Breakthrough Usability
Watch how Vault QualityDocs lets teams simply and securely manage controlled documents through the entire GxP life cycle – from creation through review and approval, and beyond.

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Veeva Vault Registrations

Global Visibility, Improved Data Quality, Better Informed Decisions
Vault Registrations provides a single global destination for planning, tracking and reporting on product registrations and health authority commitments. See how the improved visibility and data quality can streamline regulatory business operations.

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Veeva Vault Submissions

Faster Submissions, Improved Collaboration, and Continuous Visibility
See how Vault Submissions makes it easy to dynamically build and track submission content and create powerful business reports. With Vault Submissions, collaborating throughout the development and approval process has never been so simple.

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Veeva Vault Submissions Archive

Securely Access Your History of Regulatory Submissions with Vault Submissions Archive
See how Vault Submissions Archive makes it easy to secure, share, and view archived submissions and health authority correspondence from anywhere in the world.

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