R&D Demo Center

From R&D to 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 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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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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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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Vault Study Startup

Faster Time to First Patient/First Visit.
Vault Study Startup accelerates the collection, tracking, and management of study start-up activities and content by bringing together site start-up documents and site initiation in a single solution.

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Veeva Vault SiteExchange

Veeva Vault SiteExchange Demo
Veeva Vault SiteExchange makes it easy for sponsors, CROs, and investigator sites to collaborate on study activities by providing a single point of access and consistent processes for document exchange during clinical trial execution.

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Veeva VAULT EDC

Veeva Vault EDC for Clinical Data Management
See how Veeva Vault EDC’s modern interface, personalized dashboards, and easy navigation facilitates accurate data entry and streamlines clinical trial processes.

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Veeva Vault QMS

Veeva Vault QMS Demo
See how Veeva 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

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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