Veeva Vault RIM End-to-End - 6:06
End-to-end Vault RIM Demo for Large Biopharma Companies Watch how a unified Vault RIM platform can help large biopharma companies submit faster, strengthen compliance, and increase transparency.
VEEVA DEVELOPMENT CLOUD - 2:53
Connecting Vault Clinical Operations and Medical CRM Break down silos, improve coordination, and gain transparency into HCP interactions by transferring activity records between Veeva Medical CRM and Veeva Vault Clinical Operations.
Veeva Vault for Clinical Operations - 2:29
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.
Vault Study Startup Demo: Feasibility Surveys - 4:01
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 - 2:23
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 - 2:36
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 - 2:35
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 - 2:29
Streamline Study Start-up and Conduct Activities Learn how a unified clinical environment streamlines start-up and conduct activities.
Vault eTMF Demo: Part 1 - Homepage - 2:27
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 Transfer Demo - 2:12
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 RIM to Clinical Operations Connection Demo - 8:30
Vault RIM to Clinical Operations Connection Demo See how users can seamlessly transfer data and documents between regulatory and clinical Vaults using the Vault RIM to Clinical Operations Connection.
Vault CTMS Demo: Risk-based Study Management - 3:29
VEEVA VAULT CDMS - 2:27
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 Registrations - 7:43
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 - 4:49
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 - 4:45
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 - 6:06
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 - 5:42
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.
Vault Quality to RIM Connection - 13:17
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.
Veeva eConsent - 2:49
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 VAULT SAFETY - 3:30
Improve Oversight and Reduce Risk for Adverse Events See how Vault Safety leverages real-time reports and dashboards and seamless collaboration to provide visibility for risk mitigation and compliance for adverse events.
VEEVA VAULT SAFETY - 5:54
Achieve Greater Efficiencies with a Modern and Unified Safety Solution Watch how Vault Safety streamlines case management by providing one unified system for all safety information and documentation.
Veeva Vault Safety - 3:45
Streamline PSMF Management and Gain Global Visibility Simplify PSMF management for QPPVs and content owners. Easily meet regional requirements while improving inspection readiness with one global system.
Veeva Vault SafetyDocs - 3:45
Managing your PVAs, SDEAs, and Business Agreements Watch how sponsors or market authorization holders can easily collaborate with service providers on authoring, review, and oversight of pharmacovigilance agreements (PVAs), safety data exchange agreements (SDEAs), and other safety content.