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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5:30 - Vault Study Startup Demo: Feasibility Surveys

Vault Study Startup Demo: Feasibility Surveys
See how the selection process is more seamless and connected to activation with Vault Study Startup.

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Veeva Vault Study Startup: 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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Veeva Vault Study Startup: Study Startup 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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Veeva Vault Study Startup: 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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VAULT STUDY STARTUP DEMO: UNIFIED CLINICAL ENVIRONMENT

Streamline Study Start-up and Conduct Activities
Learn how a unified clinical environment streamlines start-up and conduct activities.

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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 eTMF Demo: Part 1 - Homepage

Vault eTMF Demo: Part 1 - Homepage

Gain important information about inspection readiness on the Vault eTMF homepage.
Learn how the Vault eTMF homepage gives TMF managers a view of important inspection readiness information about studies, such as milestones, completeness, timeliness, and quality.

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Vault eTMF Demo: Part 2 – TMF Completeness

Vault eTMF Demo: Part 2 – TMF Completeness

See how Vault eTMF drives efficiency and accuracy in managing TMF completeness.

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Vault eTMF Viewer Demo

The Study Differential Report
Vault eTMF Viewer allows you to manage TMF content by browsing dynamically organized content, making it easy to search, filter, and navigate within Vault.

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Vault CTMS Overview Demo

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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Vault CTMS Demo: Automation

Automate Routine Manual Tasks
Watch how Vault CTMS frees up time for CRAs and study managers by automating routine tasks in this demo.

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Monitoring Demo

Vault CTMS Demo: Monitoring

Drive Monitoring Efficiencies
Learn how Vault CTMS allows CRAs to effectively plan upcoming monitoring visits in this 3-minute video.

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Vault CTMS Demo: Milestones

Manage Milestones with Vault CTMS
Gain more control, visibility, and flexibility with study milestones using Vault CTMS.

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Vault CTMS Demo: Reporting and Dashboards

Get Visibility to Trial Progress
Learn how to easily create reports and dashboards for real-time views of study progress.

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Vault CTMS Demo: Study Oversight

Demonstrate CRO Oversight
Measure CRO performance, gain study visibility, and comply with ICH E6(R2) regulations with a modern CTMS.

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Vault EDC and Vault CTMS

Vault EDC + Vault CTMS Integration
Watch how Vault EDC seamlessly connects with Vault CTMS so you can get up-to-the-minute enrollment information, display SDV data within monitoring trip reports, and more.

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VEEVA VAULT PAYMENTS

Pay Clinical Research Sites Faster
Watch how Veeva Vault Payments enables sponsors and CROs to pay sites faster and more accurately while providing financial visibility to all study partners.

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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 CDMS

Veeva Vault EDC
See how Vault EDC provides a modern interface, personalized dashboards, and easy navigation to facilitate accurate data entry and streamline clinical trial processes.

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VEEVA SITEVAULT

eRegulatory for Clinical Research Sites
See how research sites seamlessly manage regulatory documents and information in SiteVault to reduce administrative burden, improve visibility, and speed study start-up.

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Veeva Vault QMS

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

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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

Improved Data Quality, Global Visibility, Faster Responses to Health Authorities
Vault Registrations enables companies to plan, track, and report on global product registrations and health authority correspondence and commitments within a single system. See how it works in this 4 minute demo.

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Veeva Vault Submissions

Continuous visibility, faster time to market, global alignment
Vault Submissions eliminates the need for multiple, disparate tracking systems by providing a single, authoritative source for regulatory submissions content - all in a secure cloud environment. See how it works in this 3 minute demo.

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Veeva Vault Submissions Archive

Dynamic Access Control, Faster Responses, Global Readiness
Vault Submissions Archive makes it easy to find the right information, including eCTD and non-eCTD electronic submissions, for a complete view of regulatory communications in a validated environment

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Veeva Vault RIM End-to-end

Streamline Global Regulatory Processes
Vault RIM provides an authoritative source for regulatory documents and information globally. Content and data converge in a single cloud platform that unifies registration tracking, correspondence and commitments, submission document management, dossier publishing, and regulatory submission archiving.

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VEEVA VAULT QMS

Unifying Quality and Risk Management
See how the Quality Risk Management (QRM) feature in Vault QMS allows companies to identify, assess, and mitigate strategic and operational risks, reducing quality issues and their impact.

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The Study Differential Report in Vault CDMS

See how clinical teams can use the study differential report in Vault CDMS to identify changes between studies for efficient UAT.

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