6:11 - VEEVA DEVELOPMENT CLOUD
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.
2:29 - 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.
5:30 - 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.
4:19 - Vault Study Startup Demo: 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.
2:53 - Vault Study Startup Demo: 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.
3:18 - Vault Study Startup Demo: Site Greenlight
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.
7:33 - Veeva 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.
5:04 - 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.
3:15 - VAULT CTMS MONITORING DEMO
Drive Monitoring Efficiencies
Learn how Vault CTMS allows CRAs to effectively plan upcoming monitoring visits in this 3-minute video.
2:20 - Vault CTMS Automation Demo
Automate Routine Manual Tasks
Watch how Vault CTMS frees up time for CRAs and study managers by automating routine tasks in this demo.
2:47 - VEEVA VAULT PAYMENTS
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.
2:27 - 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.
4:55 - VEEVA SITEVAULT
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.
4:57 - Veeva Vault QMS
Vault QMS Demo
See how Veeva Vault QMS easily manage all your quality processes in one
place.
6:55 - Veeva 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.
4:28 - Veeva Vault Station Manager
Overview
Watch this 4 min 28 secs video to learn how Vault Station Manager ensures the right content is always available for the right station on the manufacturing floor.
2:16 - VEEVA VAULT TRAINING
Easily Complete Training Task
Watch this 2 min 16 secs video to see how learners can easily view and complete their training tasks in Vault Training.
4:17 - 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.
3:34 - 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.
3:27 - 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
2:18 - 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.
6:40 - Vault eTMF Demo: Part 2 – TMF Completeness
See how Vault eTMF drives efficiency and accuracy in managing TMF completeness.
4:52 - CTMS CRO Oversight Demo
Measure CRO performance, gain study visibility, and comply with ICH E6 (R2)regulations with a modern CTMS.