Development Cloud Demo Center

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

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.

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.

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

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.

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

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.

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.

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.

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.

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.

TMF completeness

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

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 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 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 Automate core clinical trial processes and eliminate paper with a single suite that increases operational efficiency and reduces complexity.

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.

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

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 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.

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

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.

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.

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.

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

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.

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.

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.

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.

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

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.

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.

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.

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

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.

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.

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.

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