Development Cloud Demo Center

VEEVA DEVELOPMENT CLOUD - 13:31

Eliminate Silos, Drive Global Alignment See how Veeva Development Cloud connects end-to-end business processes across clinical, regulatory, quality, and safety for greater efficiency and compliance throughout the product lifecycle.

Veeva Vault Coder - 4:13

Veeva Vault Coder See how Veeva Vault Coder provides an intuitive interface and innovative coding tools that yield fast and accurate coding for any clinical trial.

TMF Bot Feature Demo - 3:01

AI in Veeva Vault eTMF Process documents more quickly and increase TMF quality with the TMF Bot, an artificial intelligence feature that automatically classifies uploaded and mobile-scanned documents. See it in action in Vault eTMF.

Veeva Vault for Clinical Operations - 2:29

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.

Vault Clinical Operations Global Directory Demo

Unified Vault eTMF and Vault CTMS - 3:38

Unified Vault eTMF and Vault CTMS Demo See how to improve operational efficiency and show evidence of compliance with unified Vault eTMF and Vault CTMS.

Vault Clinical Operations - 3:19

Vault Clinical Operations Global Directory Demo See how the Vault Clinical Operations Suite global directory and investigator database eliminates Excel trackers and enables document reuse, driving trial efficiencies.

Vault Clinical Operations Demo: Milestones - 4:01

Manage Milestones with Vault Clinical Operations Gain more control, visibility, and flexibility with study milestones.

Vault Study Startup Demo: Feasibility Surveys - 5:30

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

Vault Study Startup Demo: Country Intelligence - 4:19

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.

Vault Study Startup Demo: Study Startup Homepage - 2:53

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.

Vault Study Startup Demo: Site Greenlight - 2:35

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.

VAULT STUDY STARTUP DEMO: UNIFIED CLINICAL ENVIRONMENT - 6:36

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

Veeva VAULT ETMF - 7:33

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.

Vault eTMF Demo: Part 1 - Homepage - 2:27

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.

Vault eTMF Demo: Part 2 – TMF Completeness - 4:12

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

Vault eTMF Viewer Demo - 3:39

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.

TMF Transfer Demo - 2:12

TMF Transfer Enable study teams to quickly and accurately transfer TMF documents, eliminating the need for manual end-of-study migrations. With a single click, completed study country, study site, associated TMF documents, and audit trail information are seamlessly transferred between sponsor and CRO Vaults.

Vault Clinical Operations to RIM Connection Demo - 8:30

Vault Clinical Operations to RIM Connection Demo See how users can seamlessly transfer data and documents between clinical and regulatory Vaults using the Vault Clinical Operations to RIM Connection.

Vault CTMS Overview Demo - 3:51

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.

Vault CTMS Demo: Monitoring - 4:07

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

Vault CTMS Demo: Reporting and Dashboards - 4:35

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

Vault CTMS Demo: Risk-based Study Management - 3:29

Focus on Critical Study Risks See how to improve data quality, reduce operational risk, and allocate resources more effectively in Vault CTMS.

Vault CTMS Demo: Study Oversight - 4:52

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

Vault CDMS to Clinical Operations Connection - 5:06

Vault CDMS to Clinical Operations Connection 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.

VEEVA VAULT PAYMENTS - 2:47

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.

VEEVA VAULT CDMS - 2:27

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.

VEEVA SITEVAULT - 4:55

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.

Vault Quality to RIM Connection - 7:31

Streamlining Change Control and Variation Management
Veeva developed a way to streamline change control and variation management by connecting data across quality and regulatory functions for companies that have standardized on the Vault Platform. Now, teams can operate with complete impact intelligence, which improves decision making and shortens the overall timeline from change control event creation to implementation.

Veeva Vault Registrations - 4:17

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.

Veeva Vault Submissions - 3:34

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.

Veeva Vault Submissions Archive - 3:27

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

Veeva Vault RIM End-to-end - 6:31

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.