Agenda
Tuesday, September 12
Wednesday, September 13
Join Veeva to explore the latest innovations in R&D and Quality, and what lies ahead for the industry. Gain insights from industry leaders Gilead and Replimune as they share strategies that better serve patients and speed access to medical breakthroughs.
Founder and CEO
General Manager, Vault
Vice President, Development Cloud Strategy
Senior Director, Clinical Data Management
Director, Quality Information Systems
Join the regulatory zone keynote for exciting updates on the Vault RIM Suite, plus a fireside chat with Scott Cleve from Daiichi Sankyo. He’ll share his thoughts on the evolution of regulatory submissions from documents to data.
Vice President, Regulatory Operations, Information & Compliance
Vice President, Vault RIM
Vice President, Product Management Vault RIM
A top pharma quality leader breaks down the elements of driving a successful quality transformation journey across the enterprise and how it serves as a catalyst for innovation and operational excellence. Also, hear Veeva’s vision for quality, including new product announcements.
Vice President, Vault Quality & Manufacturing
Vice President, Quality Operating System, Services and Sciences
Takeda shares its vision to deliver medicines to patients faster and their achievements towards that vision. Hear practical strategies to deliver more efficient trials and better outcomes for patients, sites, and sponsors.
Vice President, Head of Innovation & Data
Vice President, Development Cloud Strategy
Join our zone keynote to discover the latest industry trends and perspectives shaping the future of Veeva Development Cloud and Vault Platform. To cap off the session, Bristol Myers Squibb’s global head of Veeva drug development and quality cloud will share insights on driving optimization and innovation in a multi-Vault environment.
Global Head, Veeva Drug Development and Quality Cloud
Development Cloud Architect, Director of Strategy
Senior Vice President, Development Cloud
Merck shares business drivers and their digital vision across safety, clinical, medical, and quality. Hear why functional areas are partnering to transform safety operations along with recent program insights, learnings, and upcoming milestones.
Senior Director, Business System Management and Innovation, PV Operations & Global Process Enablement
Director, Strategic Programs, Merck Research Laboratories IT, Merck
Vice President, Vault Safety
Vice President, Products, Vault Safety
Hear Veeva’s vision to unify the quality ecosystem at one of its most critical decision points: batch release. Learn how to accelerate decision making by bringing together quality process, content, data, and decision makers all in one platform.
Senior Director, Product Management, Vault Quality
See the Vault Clinical Operations Suite applications in action and the value of a unified platform in this live demo.
Senior Solution Consultant, Clinical Ops
Learn how global content plans expedite core document assembly for local affiliates.
Practice Manager, Vault RIM Services
Senior Product Manager, Vault RIM Submissions
See how you can leverage Study Portal and VeevaID to securely manage external users and seamlessly collaborate across internal and external teams.
Senior Product Manager
Vice President, Study Portal
Learn how emerging and midsize biopharmas can implement a safety solution in two months and manage it with limited resources.
Sr. Services Engagement Manager
Practice Director, Vault Safety
Organizations are increasingly replacing document-based training with diversified learning experiences. Learn how connected processes in Vault Training – combined with a variety of training types – increase efficiency while producing qualification and compliance.
Principal Consultant – Quality
The Veeva RTSM team will demonstrate how complex clinical trial supply scenarios can be managed through highly flexible supply management settings.
Senior Solutions Consultant
See how active dossier helps companies maintain a list of current documents for a given product and market.
Team Manager, Vault RIM
Senior Product Manager, Vault RIM Submissions
See how bringing together literature review, signal investigations, and aggregate reports simplifies signal management.
Senior Product Manager, SafetyDocs
Hear about Roche and Veeva’s experience with the FDA’s eCTD 4.0 pilot, which ended in May 2023. They’ll share what challenges they encountered, how they achieved success, and their recommended next steps for both industry and regulators.
Regulatory Data and Content Leader
Senior Manager, Regulatory Submission
Learn how Sanofi and Jazz are rolling out Submission Content Plans (SCP) to reduce dossier planning and compilation time. They’ll share about their business case, phased adoption path, tips for successful implementation, and training strategies for key stakeholders.
Senior Manager, RIM
Associate Vice President, Head of Global Submissions Management
Hear Roche’s journey to streamline end-to-end quality management with Vault Quality Suite. Get key insights from their implementation of lean business processes and modern technology to standardize quality events and content management and improve stakeholder collaboration.
Quality Director, Computer Systems Operations Chapter Lead
Director, Digital Quality Excellence
Hear how Minaris evolved from a system migration to an overhaul of their employee engagement and qualification process. Learn how to capitalize on change, and how sophisticated curricula matrices streamline competencies across shifts, products, and sites.
Global Head, Director, GxP Training, L&D
A Vault LIMS early adopter shares their progress in building a unified quality foundation for QA and QC that meets today’s requirements and will scale efficiently in the future. Hear how digitizing QC operations with Vault LIMS will maximize the value of quality, modernize and improve end user experience, and lower total cost of ownership.
Senior Director, Quality Control
Senior Director, Vault LIMS Strategy
Leaders at Xencor and Kura Oncology share how they manage sponsor-owned eTMF systems and collaborate with CRO partners. This includes how to improve existing Vault eTMF implementations, develop effective and clear oversight metrics, and more.
Director, Clinical Systems and Document Management
Senior TMF Systems Administrator
Haleon will share how they implemented the Veeva Development Cloud after completing a divestiture. They’ll review how they untangled their technology landscape, optimized processes on a new system, and built a partnership for strategic growth.
Systems, Data, and Processes Lead
Bayer shares details about their phased rollout of Vault CTMS, considerations when adding CTMS to an existing Vault eTMF deployment, and lessons learned.
Head of Systems Support
Hear directly from clinical sites about the trial supply pain points they experience and what sponsors and technology providers can do to alleviate burden.
PI / CMO
Clinical Research Nurse
Learn how Lilly’s standards-driven approach enables them to collect, aggregate, clean, and transform clinical trial data for dozens of studies per year, while benefiting from efficient workflows, automation of data checks across all sources, and delivery of just-in-time data.
Advisor, Clinical Data Strategist
Director, Clinical Results Systems
Chief Technology Officer, Vault CDMS
UCB shares their vision for Human-Centric Health that educates, empowers and enables all to actively participate in clinical research and benefit throughout the various stages of one’s health journey. Learn how an enterprise-wide ePRO solution was a key step to reduce burden on patients, caregivers, and sites while improving data quality, availability, and transparency for study teams.
Head of IT Digital Clinical Development
IT Lead Digital Clinical Solutions
General Manager, ePRO & eClinRO
Senior Vice President, Product Management, Sites & Patients
Director of Product Management, ePRO & eClinRO
Teva will discuss strategies and experiences from preparing their organization for upcoming global Vault Safety go-live. They’ll review lessons learned and recommendations for business readiness planning, process definition, data migration, training, and change management.
Head of Systems & Innovation
Senior Director, Vault Safety Strategy
Vice President, Vault Safety Services
Head of Engineering
Hear about Teva’s journey from a de-centralized eTMF, to Vault eTMF, and finally to a combined Vault eTMF/CTMS solution. Along with Daelight Solutions, they’ll share key program drivers, details on their technical approach, and how they applied creativity throughout the project to achieve success.
Senior Director, Clinical IT R&D Lead
Founder & CEO
Discover how to gain full control over your requirements, ensuring efficiency, accuracy, and traceability throughout your validation lifecycle with Validation Management.
Senior Solutions Consultant, Vault Validation Management
See how Veeva’s newest application, Link SiteBase, improves site identification and speeds enrollment with accurate real-time site data.
Vice President, Strategy, Link Clinical
Head of R&D Business Consulting, North America
See how continuous publishing streamlines activities across the Vault RIM suite.
Practice Manager, Vault Submissions Publishing
Product Expert, Submissions, Archive and Publishing
Discuss best practices for audit readiness and working with outsourcing partners to improve oversight and data visibility.
Senior Director, Vault Safety
See how uploading documents and creating data in your Vault can be as easy as sending an email.
Director, Product Management, Vault Platform
Join this discussion on improving operating models in data management — including lessons learned from Vault EDC adoption, approaches for in-house and outsourced studies, and advice for improving efficiency at organizations of all sizes.
Vice President, Clinical Data Management
Chief Data Strategist and Solutions Officer
Senior Director, Clinical Data Operations
Director, Vault CDMS Strategy
See a demo of how to establish real-time visibility into health authority approvals and speed change control and variation management processes with the Vault Quality to RIM Connection.
Solution Consultant, Quality
Learn about all the new feasibility features we’ve delivered in Vault Study Startup to make it easier than ever to identify and select sites.
Director, Strategy, Study Startup
Product Manager, Clinical Operations
Learn how to automate correspondence with health authorities to drive faster, more compliant submissions.
Senior Director, Product Management, Vault RIM
See how to streamline adverse event management and eliminate data reconciliation by bringing together clinical, safety, quality, and regulatory applications with Veeva Development Cloud.
Vice President, Product Management, Vault Safety Suite
Hear how Eli Lilly and Novo Nordisk transitioned from legacy systems to Vault Submissions Publishing. They’ll share lessons learned from three large and complex submissions, including how they updated their publishing processes to reduce submission timelines.
Senior Manager, Regulatory Affairs
Submission Manager, Regulatory Operations
Manager, Regulatory Operations
CSL shares best practices and lessons learned from establishing a unified quality ecosystem that harmonizes quality management business processes and centralizes millions of controlled documents to improve collaboration across business units. Learn how they are advancing their “Jobs To Be Done” vision for end to end batch release and complaints by bringing together manufacturing, quality and regulatory operations.
Senior Director, Information Technology
VP Of Quality
Madrigal shares their holistic quality transformation journey, including their justification for modern cloud solutions. Learn best practices, lessons learned, and how the transformation has improved quality culture, efficiency, and visibility.
Vice President, Quality Assurance
Executive Director, GMP Quality Assurance
The current technology challenges that research sites face are compounding their even bigger business problems like an increasing volume of trials, highly complex study designs, a shrinking site workforce and a shortage of operating funds. In this session, leading site experts share their challenges and insight. Learn what they need from technology to operate more efficiently and build better partnerships with their sponsors.
PI / CMO
Senior Director, Clinical Research Administration
Vice President, Strategy, Site Solutions
BeiGene and Janssen discuss how they develop new operating models supported by eTMF innovations. They’ll also analyze how new regulations and inspection trends are shaping TMF management.
Senior Director, TMF Management & Records
Associate Director, Clinical Trial Management Solutions
In this interactive session, Cerevel shares how they eliminate manual study training processes and improve compliance with Vault Study Training. They will detail how they built their business case, as well as lessons from implementation and go-live.
Manager, Quality Operations
Astellas, GSK, Regeneron, Takeda, and Vertex will share how they are each developing Veeva centers of excellence. You’ll hear strategies for implementing a new function, getting stakeholders on board, and outlining an operating maturity model to guide the overall Veeva Development Cloud journey.
Director Information & Systems Strategy
Head R&D Development (Veeva) CoE
Associate Director
Head Development Technology
Director, Business Engagement & Technology – Clinical Systems
Head of R&D Business Consulting, North America
Improve visibility into operational processes, application usage, and KPIs with advanced Vault reporting and dashboards. Get a demo on leveraging core and new capabilities to turn ideas into actionable dashboards, and learn about upcoming enhancements.
Director, Product Management, Vault Platform
Fortrea shares their experience with implementing Veeva RTSM, including reasons for adoption, collaboration on solution design and how this has helped overcome integration challenges and data errors.
Head of Global Programming and Analytics
Principal Programmer
Vice President, Strategy, Veeva RTSM
Senior RTSM Project Manager
Seagen and Merck join Veeva’s head of global quality services to discuss best practices for managing Vault implementations post-go-live. Learn how to systematically manage new releases, build a robust roadmap to realize the value of new features, establish governance within quality and other domains, and effectively engage Veeva for support.
IT Quality Director
Senior Director, IT
Learn why AbbVie decided to update their clinical data technology, and how they were able to fully implement the new system in just six months.
Global Head, Clinical Technology Strategy and Operations
Director, Clinical Data Systems (EDC & IRT)
Director Information Research
Senior Director, CDMS Strategy
Customer panel of emerging biopharmas discuss real-time data visibility and easier CRO collaboration with Vault Safety. Learn how they’re reducing operational overhead with greater control and oversight and better prepared for audits and inspections.
Head, PV Operations and Alliance Management
Senior Director, Vault Safety
Sr. Director, Global PV and Risk Management Operations
Learn how Gilead achieved simplicity and data consistency in their RIM landscape by focusing on Vault Registrations as the first step in their journey. They’ll also share information about their cross-functional collaboration model as the key to this transformation.
Director, Regulatory Affairs CMC
Senior Director, Regulatory Systems
See how Vault LIMS eliminates stand alone Lab Execution Systems (LES) and QC Electronic Lab Notebook (ELN) applications, simplifying the QC technology landscape and streamlining test execution to increase right first time.
Senior Director, Vault LIMS
Come see how Site Connect will make it possible to exchange trial information with ALL your clinical research sites.
See how Vault Registrations users can handle bulk data creation for their global product portfolios.
Principal Product Manager, Vault Registrations & MedTech
Practice Manager, Vault RIM
Join us for an industry discussion on approaches for RMP program and aRMMs tracking. We’ll discuss key requirements, planning considerations, and implementation strategies.
Managing Director
Senior Director, Vault Safety Strategy
Senior Product Manager, SafetyDocs
Management Consultant
See how to efficiently manage key GCP deviations, when identified as part of conducting a clinical trial, with Vault Quality-Vault Clinical Operations and Vault Clinical Operations-Vault CDMS Connections.
Product Manager, Vault QMS
Senior Product Manager
Learn how Atara and Krystal Bio leveraged Vault Submissions Publishing to bring breakthrough products to market. They’ll discuss how they transformed their traditional process, prepared for their Vault Submissions Publishing implementation, and developed best practices to maximize value.
Senior Director, Global Regulatory & Quality
Senior Manager, Regulatory Affairs Operations
Senior Director, Regulatory CMC and Operation
Arcus Biosciences is transforming its computer system validation program with Vault Validation Management to improve efficiency and audit readiness. Motivated by the desire to unify and automate their quality processes onto a single platform, hear about their journey through early adopter success and the drive for incremental change.
Senior Director, IT Quality Security and Compliance
Manager, IT Validation
AmplifyBio shares their journey to build a robust quality management system with standardized processes supported by modern quality systems. Hear best practices and lessons learned for establishing new quality processes, streamlining existing processes, or harmonizing across the organization and GxP disciplines to optimize use of digital systems.
System Administrator
Director, Quality Assurance
Quality Systems Supervisor
Learn to establish real-time visibility into health authority approvals and speed change control and variation management processes. Gilead shares its approach and best practices for building bi-directional information flow across quality and regulatory teams and connecting people, processes, and technology.
Senior Manager, Quality Information Systems
Learn how Amylyx shifted to managing their data in-house during a period of rapid growth. They’ll review strategies tailored to emerging biopharmas that want to get started with Veeva Development Cloud.
Head, Global Business Applications
Lead, Regulatory Affairs Strategy
Hear how Veeva is connecting product data across the Development and Commercial Cloud to support cross-Vault business process. Sarepta Therapeutics will also share how they’ve used the Vault Quality to RIM Connection to date to drive more efficient change control operations and what future benefits that connected product data will provide.
Senior Product Manager, RIM
Senior Director, Global Regulatory Operations, RIMS/DMS Lead
Director, Global GxP Quality Systems
AstraZeneca shares how their eTMF innovations drive efficiencies from study start-up to archival. Learn how to identify and implement new programs to improve document processes and become a more data-driven organization.
Transformation Director
Learn how ImmunityBio leverages Vault Clinical Operations Suite to run studies for the next generation of immunotherapies. Hear why they implemented Vault eTMF, Vault CTMS, and Vault Payments at once, lessons learned, and the value of unifying as an emerging biotech.
Vice President, Clinical Business Operations
Fortrea shares their study start-up operating model, implementation approach, lessons learned, and cycle time reductions with Vault Study Startup.
Associate Director, Business Transformation
Associate Director, Clinical Systems Operational Support
Global Head of Site Readiness and Regulatory
Join this interactive discussion to explore the trends shaping QC and how holistically transforming quality across QA and QC enables proactive quality. Hear and share best practices on forming a transformation strategy to establish an end-to-end quality foundation and maximize the value of quality.
Senior Director, Vault LIMS Strategy
Vice President, Strategy and Partnerships
Partner
Director, Digital QC
Join Veeva strategy and product experts to hear our clinical data vision and see an end-to-end digital trial demo — using Veeva Vault EDC, Veeva CDB, Veeva RTSM & Veeva ePRO.
Vice President, Strategy, Vault CDMS
Principal Solution Consultant, Clinical Data
Senior Solution Consultant, Clinical Data
Join our fireside chat to hear how AbbVie eliminated multiple safety databases with Vault Safety and is implementing Vault SafetyDocs for global PSMF and risk management.
Senior Director, Strategic Operations
Senior Director. IT – Safety, Quality, and Medical Affairs Solutions
Senior Director, Vault Safety Strategy
Hear how AstraZeneca built support for their digital regulatory transformation with strategic alignment, organizational benefits, change management, and stakeholder management. They’ll be joined on stage by the Veeva Business Consulting team who will share how to measure delivered value against the business case.
Executive Director, Global Regulatory Operations
Practice Manager, Regulatory Business Consulting
Thursday, September 14
See how continuous publishing streamlines activities across the Vault RIM suite.
Practice Manager, Vault Submissions Publishing
Product Expert, Submissions, Archive and Publishing
See how Vault Glossary gives users quick and easy access to compliant, approved definitions of key terms from within the document viewer, without having to put terms and definitions into document content.
Product Expert, Vault QualityDocs
Product Expert, Vault Platform
Network with CROs and service providers to learn ways sponsors collaborate and maintain oversight with Vault Safety.
Senior Director, Vault Safety
Hear Veeva’s vision to unify the quality ecosystem at one of its most critical decision points: batch release. Learn how to accelerate decision making by bringing together quality process, content, data, and decision makers all in one platform.
Senior Director, Product Management, Vault Quality
See how Vault Study Training brings sponsors, CROs, and research sites into a single platform to streamline and automate study training. This includes a training plan matrix to quickly assemble training needs by role and eliminate non-compliant and manual solutions.
Senior Director, Study Training
Solution Consultant
See how Vault Safety automates intake, case processing, ICSR submissions, and periodic reports with auto-coding, auto-translations, touchless case processing, and other innovations.
Principal Solutions Consultant, Safety
Learn how to shorten submission timelines by linking compliance package generation in Vault PromoMats to Vault Submissions.
Product Manager, RIM-PromoMats Connection
Practice Manager, Vault Submissions Publishing
Hear how Veeva is innovating to continue to unify quality processes across people, partners, and systems. You’ll learn what’s next for Vault Quality Suite and how we’re elevating quality beyond compliance.
Vice President, Vault Quality & Manufacturing
Vice President, Product Management, Vault Quality & Manufacturing
Explore what’s new with Vault Platform and Veeva Development Cloud. We’ll review how upcoming releases will help organizations improve scalability, user productivity, and operations. Plus, we’ll explore what’s on the roadmap for Vault Connections.
Vice President Product Management, Vault Platform & Technology
Development Cloud Architect, Director of Strategy
Product Expert, Vault Platform
Hear about recently released features and the roadmap for Vault Clinical Operations Suite. We’ll share our plans to help clinical teams streamline processes, manage global disclosures, automate training across all study partners, and more.
Vice President Product Management, Vault Clinical Operations
Product Manager, Clinical Operations
Director, Product Management, Clinical Operations
Learn how Veeva is bringing innovation to RTSM. Hear about our overall strategic vision and roadmap for this mission critical product and ask the Veeva RTSM leadership team questions during an interactive Q&A.
Director, Product Management Veeva RTSM
General Manager, Veeva RTSM
Hear the latest product updates to the Vault RIM Suite, including new roadmaps for Vault Registrations, Submissions, Submissions Publishing, and Submissions Archive.
Vice President, Product Management Vault RIM
Senior Director, Product Management, Vault RIM
Product Manager, Vault Registrations
Senior Product Manager
Senior Product Manager, Vault RIM Submissions
Senior Product Manager, Vault RIM Submissions Archive
Principal Product Manager, Vault Registrations & MedTech
Senior Product Manager, RIM
Learn what’s next for Vault CDMS, including upcoming innovations and enhancements coming to Vault EDC and Veeva CDB this year. Plus, ask the Veeva team questions during an interactive Q&A.
Chief Technology Officer, Vault CDMS
Senior Vice President, Products, Vault CDMS
Learn about the innovations and enhancements coming to Veeva ePRO and eClinRO, and ask the Veeva team questions during an interactive Q&A.
Senior Vice President, Product Management, Sites & Patients
Director of Product Management, ePRO & eClinRO
Get an overview of the Vault Safety Suite product roadmap and recent top features. We’ll share automation enhancements to speed up case processing and our vision for connecting safety to other functional areas such as regulatory and clinical.
Vice President, Product Management, Vault Safety Suite
Vice President, Products, Vault Safety
Director Product Management, Vault Safety
Senior Product Manager, SafetyDocs
Director Product Management, Vault Safety
Hear about new innovations in Vault Quality Suite to help accelerate and streamline change controls.
Senior Solution Consultant, Quality
Get all of your roadmap questions answered by our product team in this open Q&A session.
Vice President Product Management, Vault Clinical Operations
Product Manager, Clinical Operations
Director, Product Management, Clinical Operations
Get an overview of the Vault Safety Suite product roadmap and recent top features. We’ll share automation enhancements to speed up case processing and our vision for connecting safety to other functional areas such as regulatory and clinical.
Vice President, Product Management, Vault Safety Suite
Vice President, Products, Vault Safety
Director Product Management, Vault Safety
Senior Product Manager, SafetyDocs
Director Product Management, Vault Safety
Hear the latest product updates to the Vault RIM Suite, including new roadmaps for Vault Registrations, Submissions, Submissions Publishing, and Submissions Archive.
Vice President, Product Management Vault RIM
Senior Director, Product Management, Vault RIM
Product Manager, Vault Registrations
Senior Product Manager
Senior Product Manager, Vault RIM Submissions
Senior Product Manager, Vault RIM Submissions Archive
Principal Product Manager, Vault Registrations & MedTech
Senior Product Manager, RIM
Explore what’s new with Vault Platform and Veeva Development Cloud. We’ll review how upcoming releases will help organizations improve scalability, user productivity, and operations.
Vice President Product Management, Vault Platform & Technology
Development Cloud Architect, Director of Strategy
Product Expert, Vault Platform
Ask the Veeva team questions about upcoming enhancements and innovations during an interactive Q&A session.
Chief Technology Officer, Vault CDMS
Senior Vice President, Products, Vault CDMS
We’re excited to showcase our new data applications that enable sponsors and CROs to optimize trial designs with competitive protocol design intelligence and improve site identification with real-time site data. Hear our vision and roadmap for Link TrialBase and Link SiteBase and get your questions answered.
Vice President, Strategy, Link Clinical
Hear how Amylyx uses process navigator for more than just intuitive content navigation. Come discover the creative ways this can serve as a foundational tool for managing your quality program.
Head of Quality Management Systems
See how Vault CTMS helps you effectively demonstrate oversight with site communication logs, closed-loop issue management, real-time reports and dashboards, and more.
Senior Solution Consultant, Clinical Operations
See how bringing together literature review, signal investigations, and aggregate reports simplifies signal management.
Senior Product Manager, SafetyDocs
Hear how Roche is bringing together regulatory data and processes into a single, end-to-end approach. They’ll share how they are actively evolving toward a transformative state that prioritizes data-driven decisions to move the business forward.
RIM Process Lead
Senior Business Systems Lead
Join this interactive session to see demos of the latest advancements in Vault QualityDocs and Vault Station Manager, including External Collaboration for Documents, QR Code Generator, and more. You will also hear what’s next on the roadmap and get your questions answered.
Director, Product Management
Hear Veeva’s vision and roadmap for Vault QMS. Get demos of recent innovations and hear what’s next on the roadmap around topics such as intelligent automation, audits and inspections, and quality risk management (QRM). Also, Veeva’s product experts will answer your questions in this interactive session.
Senior Director, Vault Product Management, QMS
Senior Product Manager, VPS, QRM, and MedTech Quality
Hear Vault Training’s roadmap and vision, see demos of the latest innovation, and get your questions answered. Highlights will include the enhanced experience for learners, curriculum completion data, and efficient ways to manage your training matrix.
Director, Product Management
Senior Product Manager, Vault Training
Gain insight into how Vault LIMS is modernizing the QC lab to maximize right first time while improving efficiency and visibility. Get a demo of the latest capabilities, including sample management, test execution, instrument integrations, and review by exception and learn about the future vision and roadmap including a first look at stability study management.
Senior Director, Vault LIMS Strategy
Vice President, Product Management, Vault Quality & Manufacturing
Learn what tools and resources are available for Vault Admins and Developers to solve complex use cases with Vault Admin UI, Vault API, and Vault Java SDK. We’ll also review features that help customers automate deployments, integrate systems, and extend the Vault Platform.
Director, Product Management, Vault API & SDK
Associate Developer Support Engineer
GSK will share how they grant system access based on HR-designated roles and study team assignments. They’ll also explain how they authenticate sites through internal active directory and SSO, and how they plan to incoporate VeevaID into their provisioning.
Veeva CoE Service & Strategy Lead
Product Director, Site Engagement & UAM
Takeda shares their clinical trial management transformation approach and the value they’ve realized to help them deliver medicines to patients faster. Hear about critical aspects of their technical and organizational readiness workstreams – from business process design to change management, communications, and end user adoption.
Senior Manager, Process, Training, and Digital Solutions
Product Lead, Clinical Trial Management
Team Manager, R&D Business Consulting
Learn about AbbVie’s vision for improved site collaboration, and their use of Veeva products to simplify site document exchange, guarantee safety letter distribution, and improve study quality. You’ll also hear about best practices and lessons learned along the way.
Vice President of Strategy – Site Connect
Associate Director, Study Start Up Operations
Nick Darwall-Smith leverages their extensive experience in clinical trial supply to discuss how connected RTSM solutions can drive study efficiencies and explores future opportunities for innovation.
Owner
Vice President, Strategy, Veeva RTSM
See how Moderna globalized PSMF management leveraging core Vault SafetyDocs capabilities in less than 4 months. Seamlessly collaborating cross-functionally and with external reviewers and contributors, the QPPV team reduced overhead to manage and maintain specific content for local / regional requirements. They automated logbook generation, have real-time oversight, and can more easily deliver a high-quality PSMF.
Senior Director Digital PV and Clinical
Learn how Boehringer Ingelheim is engaging with sites and patients not only to address their needs in trial design and conduct but also to inform the BI digital transformation efforts and change management practices. Hear best practices from their journey and why creating meaningful strategic goals and relationships are fundamental to successfully embedding patient and site engagement practices across organizations.
Head of Patient & Site Engagement Capabilities
General Manager, ePRO & eClinRO
Alcon shares how a unified clinical data management approach reduces manual effort and ensures analysis-ready data at all times. Learn about Alcon’s journey to adopt modern approaches to support the development of clinical trial designs that capture a wide variety of modern data sources.
Head of Clinical Data Operations
Vice President, Strategy, Vault CDMS
In this two part session, AstraZeneca will share how they established new data management principles for global and affiliate markets as part of their Vault Registrations deployment. They will discuss some of the difficulties associated with implementing lasting improvements after go-live and how this shaped their change management approach. Then hear how Seagen instilled a continuous improvement model at their organization and what challenges they’ve faced with this cultural shift.
Director, Global Regulatory Operations
Senior Manager, Regulatory Information Management
Veeva shows how the Annual Product Quality Review (APQR) and Quality Management Review (QMR) features in Vault QMS help automate and streamline these time-intensive processes.
Solution Consultant
Risk-based approaches are proliferating in clinical trials, including in TMF management. Learn about Veeva’s vision for risk-based and periodic QC in Vault eTMF.
Product Manager, Vault Clinical Operations
Learn how to incorporate labeling change management into your end-to-end Vault RIM solution.
Practice Manager, Vault RIM
Product Manager, Vault Registrations
See how to streamline adverse event management and eliminate data reconciliation by bringing together clinical, safety, quality, and regulatory applications with Veeva Development Cloud.
Vice President, Product Management, Vault Safety Suite
Veeva shows how the External Collaboration features in Vault Quality Suite enable seamless and efficient collaboration with partners across multiple processes across Vault Quality Suite.
Senior Product Expert
Hear about the vision for Vault Disclosures, Veeva’s newest application to centralize and simplify global compliance operations.
Senior Director, Clinical Strategy, Vault Disclosures
Senior Product Manager, Clinical Operations
See how active dossier helps companies maintain a list of current documents for a given product and market.
Team Manager, Vault RIM
Senior Product Manager, Vault RIM Submissions
Learn how the Veeva CDB and Veeva ePRO connection allows for near-real time transfer of patient-entered data for the purpose of reconciliation with other data sources such as EDC and RTSM and the identification of trends and outliers.
Director of Product Management, ePRO & eClinRO
General Manager, CDB
See how to drive efficiency in your Vault with the latest reporting and dashboards features like Dynamic Distribution Flash Reports.
Senior Product Manager, Vault Platform Reports and Dashboards
See the latest advancements in Vault Validation Management, hear what’s next on the roadmap, and get your questions answered by an expert. You’ll learn how to optimize end-to-end validation processes to drive faster, more efficient test execution while maintaining compliance.
Director, Product Management
Explore the diverse array of new GxP training assets that we will be introducing over the next 12 months, learn how we are planning to support more of your organization’s training needs with new vertical libraries, including Corporate Compliance and EH&S, and our other plans to make life easier for you.
General Manager, LearnGxP
Hear Veeva’s vision and roadmap for Vault QMS. Get demos of recent innovations and hear what’s next on the roadmap around topics such as intelligent automation, audits and inspections, and quality risk management (QRM). Also, Veeva’s product experts will answer your questions in this interactive session.
Senior Director, Vault Product Management, QMS
Senior Product Manager, VPS, QRM, and MedTech Quality
Hear Vault Training’s roadmap and vision, see demos of the latest innovation, and get your questions answered. Highlights will include the enhanced experience for learners, curriculum completion data, and efficient ways to manage your training matrix.
Director, Product Management
Senior Product Manager, Vault Training
Join this interactive session to see demos of the latest advancements in Vault QualityDocs and Vault Station Manager, including External Collaboration for Documents, QR Code Generator, and more. You will also hear what’s next on the roadmap and get your questions answered.
Director, Product Management
Learn how to leverage Vault eTMF features to streamline document QC, including new standard fields. There will also be time to connect with Veeva’s product team for a more in-depth discussion on the future of risk-based QC in Vault eTMF.
Join Seagen for a four-year retrospective value realization journey. They’ll share their maturity growth across Clinical, Regulatory, and Quality enabling structured product and platform management via robust governance and a Veeva center of excellence.
Executive Director, Business Technology
Global Program Manager
Pharming will share how to streamline daily business interactions across regulatory and IT Roles. They’ll also review pathways and resources for developing RIM expertise and what benefits they’ve seen from their Vault RIM deployment.
Associate Director, Medical Writer
Hear from Syneos Health on how they are increasing efficiency in study delivery through a variety of operational models, and how being a partner with Veeva has enabled them to share key industry trends to support the development of a single workbench environment.
Director, R&D Advisory
Senior VP Biometrics
Hear directly from site professionals and ask questions about their experience maintaining the technology landscape of clinical trials. Hear a range of site perspectives (including a PI, seasoned executive leader, and active study coordinator) as they discuss the role technology plays in building better patient experiences — as well as their challenges, best practices, and advice for sponsors.
PI / CMO
Clinical Research Nurse
Director of Clinical Research Regulatory Affairs
Director, Vault CDMS Strategy
Vice President, Strategy, Site Solutions
Centralizing data is not enough. Centralizing data cleaning and review processes in Veeva CDB unleashes real value. Learn how with CDB’s Review Dashboard, Clean Patient Tracker, Data Provider Access, and other features made for managing data without leaving the cloud.
Senior Manager, North American Solution Consulting, Clinical Data
Join Vault Safety Suite customers to share best practices, hear from product experts, and discuss latest and upcoming Vault Safety Suite capabilities.
Senior Director, Vault Safety
Senior Product Manager, SafetyDocs
Director Product Management, Vault Safety
BASE demonstrates the necessary DevOps-integration to establish and build release automation on an enterprise-wide scale. See how to orchestrate large backlogs, configuration synchronization and deployment, testing, and alignment between enterprise projects.
Senior Manager
Senior Practice Engagement Manager
Learn how Sanofi plans to reduce regulatory dossier authoring by half in three years by leveraging lean process, unified data, and advanced technology. They will discuss their automation strategy, milestones on their journey, and their partnership approach with Veeva.
Head of Business Process & Innovation for Regulatory
Vice President, Product Management Vault RIM
Tracon will share how they gained efficiencies by integrating multiple technology systems with the Veeva Development Cloud. They’ll also explain how they created a connected clinical landscape to derive greater value from their investment.
COO
Learn how to streamline data freezing and locking with Vault EDC Snapshot. Identify a specific range of data by custom criteria like subject, status, group or cohort, dates, study events and more — then take action on that data in just clicks. Save time by working in bulk and reusing the Snapshot as data gets updated throughout the study.
Senior Manager, North American Solution Consulting, Clinical Data
Learn how to effectively validate your multi-vault environment, while simultaneously enhancing operational efficiency and ensuring regulatory compliance. Gilead Sciences and Spotline showcase their collaborative approach, leveraging state-of-the-art processes and technology to make this a reality.
Principal, Life Sciences
Senior Director, Regulatory Systems
Director Computer Systems Validation Strategy, R&D Services and Quality
Learn how Validation Management unifies validation across the Quality Suite, including QualityDocs and QMS to streamline processes and maximize efficiency.
Solution Consultant, Quality
Implementing Vault Study Startup is more than just a one-time technology deployment – you also need to align processes, teams, and continuously evolve with new features to maximize your investment. Fortrea will share best practices and key learnings about how they optimized Vault Study Startup across the key pillars of people, process, and technology.
Join Veeva Site Connect customers to share best practices, hear from product experts, and discuss latest and upcoming Site Connect capabilities.
Learn about Vault features that improve the end user experience and don’t require heavy configuration or validation to implement.
Manager, Customer Success, Quality & Regulatory
Product Expert, Vault Platform
Tracking KPIs and cycle times are key to understanding portfolio performance and driving trial efficiencies. Hear which KPIs Vertex measures to identify potential bottlenecks and areas where they can optimize monitoring. Then, engage in roundtable discussions with your peers to discuss top metrics to focus on.
Unified with Vault CTMS and connected with Vault EDC, Vault Payments simplifies payment management and enables companies to pay research sites faster. See how in this group demo.
Senior Product Manager
Join your regulatory peers for an interactive community meeting with breakout groups for popular topics.
Product Expert, Submissions, Archive and Publishing
Product Expert, Vault RIM Registrations
Learn about the innovations and enhancements coming to Veeva ePRO and eClinRO, and ask the Veeva team questions during an interactive Q&A.
Senior Vice President, Product Management, Sites & Patients
Director of Product Management, ePRO & eClinRO
Five ways to access and export Vault data to support third-party data analytics tools
Director, Product Management, Vault API & SDK
Watch how you can efficiently identify, assess, and mitigate quality risks in Vault QMS for continuous quality improvement.
Senior Product Manager, VPS, QRM, and MedTech Quality
In this demonstration, watch how using Vault EDC and Veeva RTSM together allows for a seamless connection between systems, removing the need for duplicate data entry by the site and reducing associated reconciliation efforts for data management teams.
Solution Consultant, Veeva RTSM
See how to save time and improve user experience by streamlining multiple workflows into one.
Senior Product Manager, Vault Platform
See how unified and connected quality risk management can help you improve quality, efficiency, and compliance. See a demo of the latest innovations and engage in live Q&A with the product team.
We’ll review the highlights from the Vault Platform roadmap in a shorter 50 minute session. See how upcoming releases will help organizations improve scalability, user productivity, and operations.
Vice President Product Management, Vault Platform & Technology
Product Expert, Vault Platform
Learn how Veeva is bringing innovation to RTSM. Hear about our overall strategic vision and roadmap for this mission critical product and ask the Veeva RTSM leadership team questions during an interactive Q&A.
Director, Product Management Veeva RTSM
General Manager, Veeva RTSM
Learn the ways in which customers use Vault Quality Suite to collaborate with external business partners to streamline processes and maximize efficiency.
Hear best practices for using product reference data in Vault Quality Suite, and join a roundtable discussion on customer scenarios and requirements. This session is best suited for IT and System Owners in top biopharma companies.
Learn how you can manage and conduct GxP and non-GxP training in a single LMS. This session will explore the definitions of GxP and non-GxP, and share best practices for configuration and reporting.
Learn how Veeva ePRO and Veeva eClinRO simplify the design, management, and completion of electronic patient-reported and clinician-reported outcomes.
General Manager, ePRO & eClinRO
Senior Vice President, Product Management, Sites & Patients
Director of Product Management, ePRO & eClinRO
Learn about high impact reporting capabilities, and how to leverage them for high-value reporting use cases in Vault QMS.
Learn how Atara tests and validates new functionality with each Veeva release cycle. They’ll also share strategies for streamlining some key steps in the process for more efficient technical operations.
Senior Director, Global Regulatory & Quality
Director Computer Systems Validation Strategy, R&D Services and Quality
See how Sandbox Snapshots enable users to save configurations and data for repeatable testing and faster refreshes.
Senior Product Manager, Vault Platform