Development Cloud - 2:41
Study Startup Standard Questions Demo See how the new Standard Questions feature in Veeva Study Startup streamlines feasibility and saves sites time when completing surveys to accelerate site selection.
Development Cloud - 5:03
Safety-Clinical Operations Connection Demo Discover how to automatically transfer data from Veeva Clinical Operations to Veeva Safety, for a seamless flow of safety letters to Veeva eTMF and eliminate manual study record reconciliation.
Vault SafetyDocs - 13:58
Centrally Manage Safety Content and Processes See how Vault SafetyDocs simplifies the management of pharmacovigilance system master files (PSMFs), pharmacovigilance agreements (PVAs), risk management plans (RMPs), safety signals, literature reviews, aggregate reports, and other safety-related content.
Vault SafetyDocs - 3:36
Simplify Signal Management and Safety Investigations Simplify signal management processes and safety investigations with GVP Module IX-compliant workflows that are fully integrated with MedDRA.
Vault SafetyDocs - 6:54
Streamline Aggregate Report Assembly for Better Oversight and Compliance See how to streamline the assembly of aggregate reports while collaborating with internal/external teams and maintaining oversight of aggregate report compliance.
Vault SafetyDocs - 4:07
Efficiently Manage Literature Reviews See how to manage literature reviews more efficiently and identify possible ICSRs or safety signals faster with Veeva SafetyDocs.
Veeva Safety - 5:51
Real-Time Oversight and Operational Efficiency with In-House Safety Solution See how Veeva Safety brings data insights and automated case processing in-house while keeping information secure.
Veeva Safety - 3:34
Streamline Case Processing with QC Checklists See how to generate QC checklists and operational reports in Veeva Safety. Improve efficiency and data quality by adding QC checklists to the case processing workflow.
Vault Disclosures - 2:58
Vault Disclosures Demo See how centralizing clinical trial disclosures and automating processes ensures compliant, accurate registry submissions.
Veeva Site Connect - 1:51
Site Connect Payment Information Feature Demo Sponsors and CROs can give sites visibility into expected and completed payments and equip them to reconcile invoices, improving site engagement with Veeva Site Connect.
Veeva Site Connect - 2:33
Site Connect System Links Feature Demo Sponsors and CROs can streamline site access to all study systems from a single page in Veeva Site Connect.
Veeva Site Connect - 4:34
Site Connect Automatic Document Exchange Feature Demo Sponsors and CROs can automatically send, receive, and request site documents, accelerating the document exchange process and reducing administrative burden.
Vault CDMS - 24:02
End-to-End Demo: Connecting Patients, Sites, and Sponsors/CROs Experience the power of connection on Veeva's Clinical Platform through an end-to-end demo spanning patients, sites, and sponsors/CROS.
Vault SafetyDocs - 3:17
Improve Oversight and Tracking of PVAs Easily plan, manage, and track pharmacovigilance agreements (PVAs) and partner progress toward PVA obligations using Vault SafetyDocs.
Vault SafetyDocs - 4:35
Simplify PSMF Periodic Reviews and Content Updates See how Vault SafetyDocs improves operational efficiencies by streamlining traditionally time-consuming PSMF management activities, including periodic reviews, content updates, document approval, and logbook entries.
Vault Safety - 3:18
Vault Safety Accelerated Implementation Model With Vault Safety’s accelerated implementation model, small biotechs can implement a safety solution in only 8 weeks. See how you can own your data and support PV activities such as case processing, ICSR submissions, operational reports and dashboards, and safety content management.
Vault Medical CRM - 2:53
Veeva Vault Clinical Operations to Medical CRM Connection You can now connect Vault Clinical Operations and CRM to break down silos, improve coordination, and gain transparency into HCP interactions by transferring activity records.
Vault Safety - 4:32
Global and Japan Case Processing in One Solution Easily support multilingual local ICSR reporting in one global pharmacovigilance solution including submissions for PDMA (Japan), FDA, MHRA, and EMA.
Vault Safety - 6:26
Safety-EDC Connection Demo Automate flow of serious adverse event (SAE) information between data management and safety systems for more timely responses by PV teams and streamlining of reconciliation and case processing.
Vault Submissions - 6:03
Vault RIM Global Content Plans Watch this demo to see how using Global Content Plans with Vault Registrations improves visibility and efficiency for submissions with a single, core dossier for multiple regions.
VEEVA DEVELOPMENT CLOUD - 2:43
PromoMats-Medical Connection Demo Simplify document management and enhance collaboration between medical and promotional teams.
VEEVA DEVELOPMENT CLOUD - 26:56
Veeva CDB Release Highlights | Demo See how select CDB features, including Automated Data Ingestion, Listing Builder, and Automated Query Creation, can help you automate and accelerate the ingestion, cleaning, and export of clinical data.
VEEVA DEVELOPMENT CLOUD - 3:32
Quality-Clinical Operations Connection Demo See how the Quality-Clinical Operations Connection automates the sharing of core study data and clinical issues with quality teams.
Veeva OpenData - 3:00
Veeva Network Demo Simplify master data management with an MDM built for life sciences.
Veeva OpenData - 3:00
Veeva Network Demo Simplify master data management with an MDM built for life sciences.
Veeva Site Connect - 2:18
Streamline Payment Letter Distribution Deliver payment letters and automate payment tracking for a simpler, more efficient process.
Veeva Site Connect - 5:39
Eliminate end-of-study migrations Learn how SiteConnect automates the flow of information during study closeout.
Vault Submissions - 7:10
Veeva Publishing eLearning Demo Learn how to maximize Vault Submissions Publishing with our online eLearning course.
Vault SafetyDocs - 3:47
Easily Track Changes Between PSMFs and Document Versions Learn how to easily compare individual documents or complete PSMF binders to identify changes between versions with Vault SafetyDocs.
Vault SafetyDocs - 2:55
Gain Real-time Visibility of PSMF-related Documents See how Vault SafetyDocs gives QPPVs and PSMF managers oversight and real-time visibility of PSMF-related documents with customizable reports and dashboards.
Vault Safety to Vault RIM Connection - 1:47
Vault Safety to Vault RIM Connection Demo Expedite safety cases and create better data sharing between Vault Safety and Vault RIM
Veeva Clinical Operations - 2:18
Streamline Site Feasibility and Selection Streamline the site feasibility and selection process with accurate site and investigator data and fewer requests of sites.
Veeva Clinical Operations - 2:54
Accelerate Site Activation with Simplified Processes Accelerate site activation with a simplified experience for site login, training, and document exchange, as well as reporting on progress toward greenlight.
Veeva Clinical Operations - 2:52
Improve Site Monitoring and Payment Reconciliation Reduce variation in monitoring practices, increase visibility into monitoring activities, and expedite site payment reconciliation.
Vault Clinical Operations - 3:50
Vault Clinical Operations See how study teams can automatically create and classify content from emails, including both email communications and attachments.
VEEVA VAULT RIM - 3:05
Document Templates and Tokens Learn how document templates and tokens help accelerate the document authoring process.
Vault Study Startup - 2:46
Vault Study Startup: Reports and Dashboards See how to get real-time visibility to metrics and milestones on the critical path in Vault Study Startup.
Vault Study Training - 3:09
Study Training Impact Assessments Feature Demo See how you can leverage impact assessments to track modifications to documents — including protocol amendments — and update study training requirements.
Vault Clinical Operations - 2:03
Track, Manage, and Report on Quality Issues See how to easily track, manage, and report on quality issues in Vault eTMF and Vault Study Startup.
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.
Vault CDMS - 2:10
Veeva CDB Overview Demo See how Veeva CDB simplifies the aggregation, cleaning, and preparation of Clinical Data
VEEVA DEVELOPMENT CLOUD - 3:02
Vault Study Training Overview Demo Brings sponsors, CROs, and research sites into a single platform.
VEEVA DEVELOPMENT CLOUD - 2:26
Veeva eCOA Demo Build studies faster and smarter with Veeva eCOA.
Veeva eClinRO - 2:10
Simplify eClinRO Management with Veeva eCOA Simplify eClinRO capture with a simple, web-based application for sites to access, complete, and manage assessments.
VEEVA DEVELOPMENT CLOUD - 2:15
MyVeeva for Patients Demo MyVeeva for Patients makes taking part in a clinical trial more accessible and convenient.
VEEVA DEVELOPMENT CLOUD - 4:19
Vault RIM to PromoMats Connection Learn how to shorten submission timelines by linking compliance package generation from Vault Submissions to Vault PromoMats.
VEEVA DEVELOPMENT CLOUD - 13:31
Eliminate Silos, Drive Global Alignment See how Veeva Development Cloud connects end-to-end business processes across clinical, regulatory, quality, and safety for greater efficiency and compliance throughout the product lifecycle.
Veeva Vault Coder - 4:13
Veeva Vault Coder See how Veeva Vault Coder provides an intuitive interface and innovative coding tools that yield fast and accurate coding for any clinical trial.
TMF Bot Feature Demo - 3:01
AI in Veeva Vault eTMF Process documents more quickly and increase TMF quality with the TMF Bot, an artificial intelligence feature that automatically classifies uploaded and mobile-scanned documents. See it in action in Vault eTMF.
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.
Unified Vault eTMF and Vault CTMS - 3:38
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 - 3:19
Vault Clinical Operations Global Directory Demo See how the Vault Clinical Operations global directory and investigator database eliminates Excel trackers and enables document reuse, driving trial efficiencies.
Vault Clinical Operations Demo: Milestones - 4:01
Manage Milestones with Vault Clinical Operations Gain more control, visibility, and flexibility with study milestones.
Vault Study Startup: Standard Metrics Demo - 1:05
Vault Study Startup: Standard Metrics Demo Find out how Vault Study Startup can help you measure cycle times to optimize processes in this short demo.
Vault Study Startup Demo: Feasibility Surveys - 5:30
Vault Study Startup Demo: Feasibility Surveys See how the selection process is more seamless and connected to activation with Vault Study Startup.
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: Site Greenlight - 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 - 6:36
Streamline Study Start-up and Conduct Activities Learn how a unified clinical environment streamlines start-up and conduct activities.
Veeva VAULT ETMF - 3:30
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. Contact us to see a demo and explore the full capabilities of Vault eTMF.
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.
Vault eTMF Demo: Part 2 – TMF Completeness - 4:12
TMF completeness See how Vault eTMF drives efficiency and accuracy in managing TMF completeness.
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 Clinical Operations for CROs - 2:37
Vault Clinical Operations for CROs Automate core clinical trial processes and eliminate paper with a single suite that increases operational efficiency and reduces complexity.
Vault CTMS Overview Demo - 3:51
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.
Vault CTMS Demo: Monitoring - 4:07
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 - 4:35
Get Visibility to Trial Progress Learn how to easily create reports and dashboards for real-time views of study progress.
Vault CTMS Demo: Risk-based Study Management - 3:29
Focus on Critical Study Risks See how to improve data quality, reduce operational risk, and allocate resources more effectively in Vault CTMS.
Vault CTMS Demo: Study Oversight - 4:52
Demonstrate CRO Oversight Measure CRO performance, gain study visibility, and comply with ICH E6(R2) regulations with a modern CTMS.
Vault CTMS Demo: Study Oversight - 4:52
Demonstrate CRO Oversight Measure CRO performance, gain study visibility, and comply with ICH E6(R2) regulations with a modern CTMS.
Vault Clinical Operations to CDMS Connection - 5:06
Vault Clinical Operations to CDMS 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 PAYMENTS - 2:47
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.
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 SITEVAULT - 4:55
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.
Vault Quality to RIM Connection - 7:31
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 Vault Registrations - 4:17
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 - 3:34
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 DEMO - 11:26
Veeva Vault Submissions Publishing See how Vault Submissions Publishing enables users to manage content planning in preparation for health authority submission.
Veeva Vault Submissions Archive - 3:27
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 - 6:31
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.
Veeva Vault RIM - 5:54
Active Dossier in Vault RIM See how active dossier helps users maintain a list of current documents for a given product and market.
Vault RIM - 8:55
Vault RIM Submission Content Plans Submission content plans enable Vault RIM users to auto-generate a table of contents for major regulatory submissions, add planned content, and report on submission status in real time.
Vault CDMS - 4:30
Data Entry for Sites in Vault CDMS See how Vault CDMS simplifies data entry for sites, prioritizes work to be done, and automatically saves data for a better user experience.
Vault EDC - 3:15
COVID-19 Study Template in Vault EDC Get your COVID-19 study up and running in days with a fully validated template study that follows the new FDA guidelines based on CDC and ISARIC recommendations.
Vault CDMS - 2:30
The Study Differential Report in Vault CDMS See how clinical teams can use the study differential report in Vault CDMS to identify changes between studies for efficient UAT.
Veeva Vault Connector - 2:32
Mulesoft Veeva Vault Connector Demo See how the MuleSoft Veeva Vault Connector makes it easy to move data.
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 Vault Safety Docs - 6:09
Gain Control of Your Safety Documentation Watch how Vault SafetyDocs easily manages pharmacovigilance content and enables global collaboration for greater efficiency and compliance.
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 SafetyDocs - 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.
Veeva Site Connect - 2:38
Exchanging Regulatory Packages with Sites See how Veeva Site Connect automates the flow of trial information with clinical research sites to speed study start-up in this demo.
Veeva Site Connect - 3:50
Safety Letter Distribution See how to automate and streamline the safety letter distribution process with Veeva Site Connect in this 3-minute demo.