Development Cloud Demo CenterFrom clinical trials to quality and manufacturing, Veeva’s cloud-based content management applications are developed specifically for the global life sciences industry. See how different content management in the cloud can be by taking a look at the sneak peeks below, then be sure to contact us for more information.
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: Country Intelligence - 4:19
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.
Vault Study Startup Demo: Study Startup Homepage - 2:53
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.
VAULT STUDY STARTUP DEMO: UNIFIED CLINICAL ENVIRONMENT - 6:36
Streamline Study Start-up and Conduct Activities Learn how a unified clinical environment streamlines start-up and conduct activities.
Veeva VAULT ETMF - 7:33
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 - 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 Clinical Operations to RIM Connection Demo - 8:30
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 CTMS Demo: Risk-based Study Management - 3:29
Vault CDMS to Clinical Operations Connection - 5:06
Vault CDMS to Clinical Operations 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 - 2:27
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.
Vault Quality to RIM Connection - 7:31
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 Vault Registrations - 4:17
Data Quality, Global Visibility, Faster Responses to Health
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 - 3:34
visibility, faster time to market, global
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 - 3:27
Access Control, Faster Responses, Global
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 - 6:31
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
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 Safety - 5:55
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 - 6:37
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 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 - 3:43
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 - 3:42
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.