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.


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.

Veeva Vault Coder

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

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

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.


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

Unified Vault eTMF and Vault CTMS

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

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

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

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.

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.

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.

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.


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



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

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.

Vault eTMF Demo: Part 2 – TMF Completeness

Vault eTMF Demo: Part 2 – TMF Completeness

TMF completeness

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

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.

TMF Transfer Demo

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

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 Clinical Operations Suite for CROs

Vault Clinical Operations Suite for CROs Automate core clinical trial processes and eliminate paper with a single suite that increases operational efficiency and reduces complexity.


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.

Monitoring Demo

Vault CTMS Demo: Monitoring

Drive Monitoring Efficiencies Learn how Vault CTMS allows CRAs to effectively plan upcoming monitoring visits in this 4-minute video.

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.

Vault CTMS Demo: Risk-based Study Management

Vault CTMS Demo: Risk-based Study Management

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

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

Vault EDC to Vault CTMS Connection

Vault EDC to Vault CTMS 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.



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.



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 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.



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.


Veeva Vault QMS

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


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.

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.


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.


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

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.

Veeva Vault RIM

Optimize Resources with Submission Forecasting With dynamic reports and dashboards, regulatory teams gain real-time access to submission forecasts so they can better allocate resources. Watch this demo to learn more.

Veeva Vault RIM

Improve Performance with Regulatory Metrics Vault RIM dashboards increase visibility into critical metrics so regulatory teams can make faster, more informed decisions. Watch this demo to learn more.

Veeva Vault RIM

NeeS Publishing and CTA Content Plans in Vault RIM
Learn how continuous publishing works for non-eCTD submissions including how to leverage additional submission content plan templates and reuse content plans for publishing CTAs to new countries.

Veeva Vault RIM

Active Dossier in Vault RIM
See how active dossier helps users maintain a list of current documents for a given product and market.

Vault RIM Suite

Vault RIM Submission Content Plans
Submission content plans enable Vault RIM users to auto-generate a table of contents for major regulatory submissions, add planned content, and report on submission status in real time.



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.

Vault Quality to RIM Connection Demo

Vault Quality to RIM Connection

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.

Vault CDMS

The Study Differential Report in Vault CDM

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

Veeva Vault Connector

Mulesoft Veeva Vault Connector Demo See how the MuleSoft Veeva Vault Connector makes it easy to move data.

Veeva eConsent

Provide a Simple and Effective Consenting Process to Reduce Administrative Burden and Trial Execution Time Veeva eConsent delivers a better patient experience through an end-to-end informed consent process that reduces administrative burden for sites and study teams.

Veeva Site Connect

Veeva Site Connect

Inviting a Site to Participate in a Study Watch this 3-minute demo on inviting a clinical research site to participate in a controlled, connected study.

Veeva Site Connect

Veeva Site Connect

Exchanging Regulatory Packages with Sites See how Veeva Site Connect automates the flow of trial information with clinical research sites to speed study start-up in this demo.

Veeva Site Connect

Veeva Site Connect

Safety Letter Distribution See how to automate and streamline the safety letter distribution process with Veeva Site Connect in this 3-minute demo.