Development Cloud Demo Center
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.
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: 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.
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.
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
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
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 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: 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.
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.
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 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 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
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 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.
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.
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.