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.
6:36 - 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.
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.
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.
2:12 - Vault eTMF to Vault Submissions Connection Demo
Vault eTMF to Vault Submissions Connection Demo
See how users can seamlessly transfer data and documents between clinical and regulatory Vaults using the Vault eTMF to Vault Submissions connection.
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.
7:31 - Vault QMS to Vault Registrations 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.
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
6:31 - 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.