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.
Veeva SafetyDocs - 13:58
Centrally Manage Safety Content and Processes See how Veeva 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.
Veeva 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.
Veeva 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.
Veeva 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.
Veeva Disclosures - 2:58
Veeva 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.
Veeva 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.
Veeva SafetyDocs - 3:17
Improve Oversight and Tracking of PVAs Easily plan, manage, and track pharmacovigilance agreements (PVAs) and partner progress toward PVA obligations using Veeva SafetyDocs.
Veeva SafetyDocs - 4:35
Simplify PSMF Periodic Reviews and Content Updates See how Veeva SafetyDocs improves operational efficiencies by streamlining traditionally time-consuming PSMF management activities, including periodic reviews, content updates, document approval, and logbook entries.
Veeva Safety - 3:18
Veeva Safety Accelerated Implementation Model With Veeva 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.
Veeva Medical CRM - 2:53
Veeva Clinical Operations to Medical CRM Connection You can now connect Veeva Clinical Operations and CRM to break down silos, improve coordination, and gain transparency into HCP interactions by transferring activity records.
Veeva 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.
Veeva 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.
Veeva Submissions - 6:03
Veeva RIM Global Content Plans Watch this demo to see how using Global Content Plans with Veeva 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.
Veeva Submissions - 7:10
Veeva Publishing eLearning Demo Learn how to maximize Veeva Submissions Publishing with our online eLearning course.
Veeva 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 Veeva SafetyDocs.
Veeva SafetyDocs - 2:55
Gain Real-time Visibility of PSMF-related Documents See how Veeva SafetyDocs gives QPPVs and PSMF managers oversight and real-time visibility of PSMF-related documents with customizable reports and dashboards.
Veeva Safety to Veeva RIM Connection - 1:47
Veeva Safety to Veeva RIM Connection Demo Expedite safety cases and create better data sharing between Veeva Safety and Veeva 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.
Veeva Clinical Operations - 3:50
Veeva Clinical Operations See how study teams can automatically create and classify content from emails, including both email communications and attachments.
VEEVA RIM - 3:05
Document Templates and Tokens Learn how document templates and tokens help accelerate the document authoring process.
Veeva Study Startup - 2:46
Veeva Study Startup: Reports and Dashboards See how to get real-time visibility to metrics and milestones on the critical path in Veeva Study Startup.
Veeva 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.
Veeva Clinical Operations - 2:03
Track, Manage, and Report on Quality Issues See how to easily track, manage, and report on quality issues in Veeva eTMF and Veeva Study Startup.
Veeva RIM End-to-End - 6:06
End-to-end Veeva RIM Demo for Large Biopharma Companies Watch how a unified Veeva RIM platform can help large biopharma companies submit faster, strengthen compliance, and increase transparency.
Veeva 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
Veeva 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
Veeva RIM to PromoMats Connection Learn how to shorten submission timelines by linking compliance package generation from Veeva Submissions to Veeva 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 Coder - 4:13
Veeva Coder See how Veeva 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 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 Veeva 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 Veeva eTMF and Veeva CTMS - 3:38
Unified Veeva eTMF and Veeva CTMS Demo See how to improve operational efficiency and show evidence of compliance with unified Veeva eTMF and Veeva CTMS.
Veeva Clinical Operations - 3:19
Veeva Clinical Operations Global Directory Demo See how the Veeva Clinical Operations global directory and investigator database eliminates Excel trackers and enables document reuse, driving trial efficiencies.
Veeva Clinical Operations Demo: Milestones - 4:01
Manage Milestones with Veeva Clinical Operations Gain more control, visibility, and flexibility with study milestones.
Veeva Study Startup: Standard Metrics Demo - 1:05
Veeva Study Startup: Standard Metrics Demo Find out how Veeva Study Startup can help you measure cycle times to optimize processes in this short demo.
Veeva Study Startup Demo: Feasibility Surveys - 5:30
Veeva Study Startup Demo: Feasibility Surveys See how the selection process is more seamless and connected to activation with Veeva Study Startup.
Veeva 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 Veeva Study Startup.
Veeva Study Startup Demo: Study Startup Homepage - 2:53
Improve Visibility of Study Start-up Progress See how Veeva Study Startup gives study start-up specialists and managers complete visibility into critical milestones, tasks, and activities with a dedicated homepage.
Veeva Study Startup Demo: Site Greenlight - 2:35
Streamline and Standardize Site Greenlighting Learn how Veeva Study Startup makes it easy to efficiently manage the site greenlight process through visualization, collaborative review, and actionable insights.
VEEVA 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 ETMF - 3:30
Streamline Document Collection, Management, and Analysis Take a quick look inside Veeva 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 Veeva eTMF.
Veeva eTMF Demo: Part 1 - Homepage - 2:27
Gain Important Information about Inspection Readiness on the Veeva eTMF Homepage Learn how the Veeva eTMF homepage gives TMF managers a view of important inspection readiness information about studies, such as milestones, completeness, timeliness, and quality.
Veeva eTMF Demo: Part 2 – TMF Completeness - 4:12
TMF completeness See how Veeva 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.
Veeva RIM to Clinical Operations Connection Demo - 8:30
Veeva RIM to Clinical Operations Connection Demo See how users can seamlessly transfer data and documents between regulatory and clinical Vaults using the Veeva RIM to Clinical Operations Connection.
Veeva Clinical Operations for CROs - 2:37
Veeva Clinical Operations for CROs Automate core clinical trial processes and eliminate paper with a single suite that increases operational efficiency and reduces complexity.
Veeva CTMS Overview Demo - 3:51
Enable Faster, Higher-Quality Trials Take a peek at how Veeva CTMS makes it easy for life sciences companies to unify clinical information, streamline processes, and gain complete visibility across the clinical trial portfolio.
Veeva CTMS Demo: Monitoring - 4:07
Drive Monitoring Efficiencies Learn how Veeva CTMS allows CRAs to effectively plan upcoming monitoring visits in this 4-minute video.
Veeva 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.
Veeva 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 Veeva CTMS.
Veeva 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.
Veeva 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.
Veeva Clinical Operations to CDMS Connection - 5:06
Veeva Clinical Operations to CDMS Connection Watch how Veeva EDC seamlessly connects with Veeva CTMS so you can get up-to-the-minute enrollment information, display SDV data within monitoring trip reports, and more.
VEEVA PAYMENTS - 2:47
Pay Clinical Research Sites Faster Watch how Veeva Payments enables sponsors and CROs to pay sites faster and more accurately while providing financial visibility to all study partners.
VEEVA CDMS - 2:27
Veeva 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. Veeva 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.
Veeva 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 QMS - 7:31
Streamlining Change Control Across Quality and Regulatory See how Veeva Quality to RIM Connection automates cross-functional change control processes enabling quality teams to make more-informed decisions and optimized changes to approved products, manufacturers, and suppliers.
Veeva Registrations - 4:17
Improved Data Quality, Global Visibility, Faster Responses to Health Authorities Veeva 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 Submissions - 3:34
Continuous visibility, faster time to market, global alignment Veeva 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 SUBMISSIONS DEMO - 11:26
Veeva Submissions Publishing See how Veeva Submissions Publishing enables users to manage content planning in preparation for health authority submission.
Veeva Submissions Archive - 3:27
Dynamic Access Control, Faster Responses, Global Readiness Veeva 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 RIM End-to-end - 6:31
Streamline Global Regulatory Processes Veeva 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 RIM - 5:42
NeeS Publishing and CTA Content Plans in Veeva 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 RIM - 5:54
Active Dossier in Veeva RIM See how active dossier helps users maintain a list of current documents for a given product and market.
Veeva RIM - 8:55
Veeva RIM Submission Content Plans Submission content plans enable Veeva RIM users to auto-generate a table of contents for major regulatory submissions, add planned content, and report on submission status in real time.
Veeva CDMS - 4:30
Data Entry for Sites in Veeva CDMS See how Veeva CDMS simplifies data entry for sites, prioritizes work to be done, and automatically saves data for a better user experience.
Veeva EDC - 3:15
COVID-19 Study Template in Veeva 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.
Veeva CDMS - 2:30
The Study Differential Report in Veeva CDMS See how clinical teams can use the study differential report in Veeva CDMS to identify changes between studies for efficient UAT.
Veeva Connector - 2:32
Mulesoft Veeva Connector Demo See how the MuleSoft Veeva Connector makes it easy to move data.
Veeva Safety - 5:55
Improve Oversight and Reduce Risk for Adverse Events See how Veeva Safety leverages real-time reports and dashboards and seamless collaboration to provide visibility for risk mitigation and compliance for adverse events.
Veeva Safety - 6:37
Achieve Greater Efficiencies with a Modern and Unified Safety Solution Watch how Veeva Safety streamlines case management by providing one unified system for all safety information and documentation.
Veeva Safety Docs - 6:09
Gain Control of Your Safety Documentation Watch how Veeva 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 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 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.