Powerful Community, Fresh Ideas
Tuesday, 3 June
Join us at an invite-only dinner at Kalma restaurant to celebrate the outstanding contributions of clinical research sites.
Wednesday, 4 June
In the Opening Keynote, Veeva will share its R&D and Quality vision, highlighting advancements in Veeva AI, Development Cloud, and Quality Cloud. Leaders from Novo Nordisk and Recipharm will join to discuss the future of new medicine and therapy development and manufacturing.
Digital Transformation Officer, Drug Development
Head of Quality Management and Regulatory Affairs
Hear Bayer’s journey to simplify its clinical infrastructure. As an early adopter in Clinical, learn how it pioneered a clinical platform strategy and improved efficiency across clinical operations and data. This includes a “customer-centric” approach to manage change in partnership with sites.
Head, Clinical Digital Innovation
Senior Vice President, Clinical Strategy
Learn from a leading CDMO how the evolving industry ecosystem impacts quality management across partners. Hear about opportunities and challenges of collaboration.
Global Head Strategic Quality Management
Vice President Quality Cloud, Europe
MSD discusses how they are innovating their pharmacovigilance operations and improving efficiency within safety teams and across functions. Hear how they are building a trusted data foundation to fuel advanced automation.
Director, Business System Management & Innovation
Vice President, Veeva Safety
Sr. Director Veeva Safety – Europe
In an ever-changing regulatory landscape, innovation and agility are essential. Understand how both internal and external drivers are shaping Teva’s future and how they use Veeva RIM, Development Cloud, and Quality Cloud to drive efficiency, transform business operations, and stay ahead of evolving HA standards. Gain insights on adopting a data-driven, change as usual mindset for RIM excellence.
Vice President Regulatory Operations
Vice President Regulatory, Europe
Novo Nordisk shares strategy on accelerating clinical trials and product launches with Development Cloud. Central to its approach is bringing business and IT teams together through a single platform to improve user experience while enabling cross-collaboration, process automation, and data standards.
Senior Director, Development Cloud Strategy
Vice President of Product Management, Vault Platform
Vice President
See how Veeva Clinical Operations improves study partnerships by streamlining document exchange and safety letter distribution, automating training, and reducing administrative burden.
Solution Consultant
Discover how the connection between EDC and Safety automates the transfer of serious adverse event (SAE) information, eliminating manual data entry for safety teams and reducing the time and effort spent on reconciliation by data managers.
Solution Consultant, Clinical Data
Discover strategies for optimizing cross-functional workflows in life sciences, and how the Veeva Industry Cloud supports end-to-end processes across multiple applications.
Senior Manager, EU DevCloud Strategy
Explore the benefits of accelerating deviation data sharing across the CDMO-sponsor interface, highlighting how real-time collaboration can enhance product quality, expedite batch release, and strengthen compliance readiness.
Senior Director, Strategy – Veeva QMS
Learn about recent updates designed to streamline and enhance change management processes. Discover how the QMS-RIM Connector improves efficiency and facilitates data sharing between Veeva Quality and Veeva RIM.
Senior Product Manager, RIM Connections
The Site Meet and Greet offers a unique opportunity for sponsors, clinical research sites, and CROs to connect and exchange insights. Join us to foster meaningful relationships that can lead to future collaboration.
VP of Strategy, Site Solutions
Senior Director, Site Connect Strategy
Discover how this connection eliminates transcription errors, duplicate data entry, and manual tasks with automatic data transfer between EDC and CTMS. Learn how to automate the creation of protocol deviations and payments, and streamline operations with real-time data visibility.
Senior Solution Consultant, Clinical Data
Discover how to harmonize content and improve real-time oversight for QPPVs to stay inspection-ready. Easily manage multiple local PSMFs across regions by reusing global content.
Principal Product Manager, Veeva AI (Safety)
Discover how VeevaID simplifies clinical research site user authentication to all Veeva systems with one SSO login.
Senior Director, Development Cloud Strategy
Discover how to make your refresher training more effective, efficient, and engaging. Learn best practices for managing refresher content and assignments, and get a preview of upcoming features designed to enhance the refresher training experience.
General Manager Veeva LearnGxP
Director, Training Strategy
Learn how Veeva experts help small to mid-sized biopharmas maximize Veeva RIM value through Continuous Innovation – guiding teams in building strategic roadmaps and preparing for smarter feature adoption, expanded usage, and optimal impact.
Principal Consultant and Services Lead, Continuous Innovation, Regulatory
Hear the roadmap and vision for Veeva eTMF and Veeva Study Startup. See demos of the latest innovations and get your questions answered.
Senior Product Manager, Clinical Operations
Hear the roadmap and vision for Veeva Study Training. See demos of the latest innovations and get your questions answered.
Senior Product Manager
Learn what’s next for Veeva EDC, CDB, and eCOA. Hear recent innovations and upcoming enhancements as we deliver for patients, sites, and sponsors. Join the interactive Q&A of your choice in the follow-up discussion.
SVP Product Management, Sites and Patients
Senior Vice President of Product, Clinical Data
Share and learn best practices to adopt new features, like Quick Queries. Gain valuable insights from experienced Veeva customers, Product Experts and services leads about EDC/CDB release management across customers. Exchange your success stories and discuss pain points with your peers and the Veeva team. Open to Veeva Clinical Data customers only.
Director, Product Expert, Clinical
Senior Director, Strategy, Clinical Data
Hear the roadmap and vision of Veeva QMS. See demos of the latest innovations and get your questions answered.
Senior Director, Vault Product Management, QMS
Learn about Veeva’s GxP training vision and roadmap, see demos of the latest innovations, and get your questions answered.
Senior Product Manager
General Manager Veeva LearnGxP
See recent innovations in global case processing automation, narrative optimization, and operational metrics. We’ll also share how we’re solving for unstructured intake and a preview of how Veeva Safety Workbench and Veeva Safety Signal unlock the full potential of a single unified safety platform.
Vice President, Product Management, Veeva Safety
Hear about key Veeva Registrations, Submissions, Submissions Publishing, and Submissions Archive features that were delivered over the past year, highlights from this year’s roadmap, and how we’re helping biopharmas achieve end-to-end process excellence. We’ll also provide progress updates on eCTD 4.0, Active Dossier, our Global Content Plan connection, and other features designed to reduce data management efforts.
Vice President, Product Management, Regulatory
Discover how Vault Platform advancements improve performance, simplify configuration, and enable innovation. See ways to leverage process monitor, Word formatted outputs, and action triggers as well as get a preview of upcoming enhancements to security, reporting, and Direct Data API.
Vice President of Product Management, Vault Platform
Hear the roadmap and vision for Veeva CTMS and Veeva Payments. See demos of the latest innovations and get your questions answered.
Senior Product Manager, Clinical Operations
Hear the roadmap and vision for Veeva Site Connect. See demos of the latest innovations and get your questions answered.
Director of Product, Clinical Operations
Immediately following the Clinical Data roadmap, join Veeva’s product team for a Q&A on Veeva EDC and CDB. Have a question about Quick Queries or Observations? Curious about plans to support risk-based data management? This is your chance to get real-time insights from the teams shaping the future of EDC and CDB.
Senior Vice President of Product, Clinical Data
Director, Product Management, EDC
VP Product, Veeva CDB
Immediately following the Clinical Data roadmap join Veeva’s eCOA product team for a deep dive Q&A in to recently released features and discussion on the upcoming plans.
SVP Product Management, Sites and Patients
Join a panel of industry experts as they share insights on fostering collaboration across internal and external teams. Discover how Veeva enables more efficient, reliable workflows, enhances traceability, and simplifies processes.
Global Head Quality & HSE Solutions
Group Quality and Regulatory Manager
Head of Quality Management and Regulatory Affairs
Strategy Director, Quality & Manufacturing
Senior Director, Veeva Regulatory Strategy
Join our Veeva Safety product team for live roadmap Q&A.
Vice President, Product Management, Veeva Safety
Vice President Product Architect, Veeva Safety
Principal Product Manager, Veeva AI (Safety)
Director Product Management, Veeva Safety Signal & Workbench
See how regulatory teams use Global Content Plans to reduce cycle times to complete submission activities. Learn to optimize dispatch processes and update cycles from core packages to local submissions.
Solution Consultant, Regulatory
Discuss with peers on experiences with deploying Veeva Connections. Share successes, challenges, and value added with peers in the industry. Veeva teams will also be available for feedback and guidance.
Senior Director, Development Cloud Strategy
Roundtable discussion with peers on experiences and best practices utilizing Veeva Open Source tools to develop connectors with 3rd party systems. Recommended for Vault Administrators or Developers.
Director of Product Management, Developer Experience
See how Digital Process Assistants (personified AI agents) assist end users in rapidly answering complex queries and finding relevant information across SOPs, knowledge articles, LMS platforms, and study databases.
R&D Practice Leader EMEA and APJ
Following the Regulatory roadmap session, join the Veeva RIM product team for Q&A and discussions on key features from the past year, the latest in regulatory guidelines and developments, and the future roadmap for Veeva RIM.
Vice President, Product Management, Regulatory
Generate documents from Vault data with the new Microsoft Word formatted outputs. See how to configure, test, and easily use it to display data in specific formats.
Senior Director or Product, Vault Platform
GSK and AstraZeneca share their vision to enhance research site collaboration with Veeva Site Connect. Learn about their implementation approach, success streamlining safety letter distribution and other site-facing processes, and future plans.
eTMF/Site Connect Product Owner
Global Clinical Solutions Senior Director
Senior Director, Site Connect Strategy
Ipsen details how adopting a sponsor-owned eTMF system improved process efficiency and regulatory compliance. Learn best practices for advocating a sponsor-owned eTMF business case and how to facilitate collaboration with CROs to further inspection readiness.
eTMF Systems Manager
Senior System Data Lead
Boehringer Ingelheim transformed its ways of working, shortened cycle times, and established a foundation for innovation. Hear practical tips to automate data cleaning and simplify builds. Learn ways to drive value beyond data management, including optimizing connections and processes with Clinical Operations.
Senior Director, Clinical Strategy
Capability Owner Clinical Data Collection
Hear the roadmap and vision of Veeva LIMS. See demos of the latest innovations and get your questions answered.
Director, Product Management,
Hear Veeva’s vision and roadmap to modernize and accelerate validation management processes. See demos of the latest features in Veeva Validation Management and get your questions answered.
Senior Product Manager, Validation Management
Hear the roadmap and vision for Veeva QualityDocs and Veeva Station Manager, see demos of the latest innovations, and get your questions answered.
Director, Product Management (QualityDocs, Station Manager & Training)
Discover how Camurus improved control and data quality for better oversight. Gain insights into its phased approach to bringing pharmacovigilance operations and technology in-house, and best practices for implementing your own safety solution.
Director Patient Safety/QPPV
Speed and efficiency are critical to achieving world-class RIM operations. Learn how Alvotech enhanced process performance, accelerated product launches, and reshaped roles and responsibilities with a proactive and adaptable approach to change. Discover key publishing success metrics and practical considerations for small biopharmas navigating regulatory process transformation.
Director Regulatory Information Management
Gain insights from Roche’s Active Dossier implementation journey – including drivers behind adoption, current progress, key learnings, and future plans. Discover how Roche is laying the foundation for continued innovation in regulatory operations.
Regulatory Program Director
IT Product Manager
Get a preview of Veeva AI and Agent use cases in the Development Cloud and Quality Cloud applications. Understand how AI in the platform and embedded into applications will enable broad adoption to help users analyze data, draft documents, and extract information out of unstructured content.
SVP, Veeva AI Solutions
Learn how Veeva CTMS supports complex clinical trials. This includes enabling the subdivision of subjects into distinct groups to enhance the organization and granularity of key trial activities.
Solution Consultant, Clinical Operations
Learn how smaller biotechs can maximize the value of existing applications to improve inspection readiness in preparation for ICH E6 (R3). We will share strategies for prioritizing needs and building a feature adoption roadmap. Limit 20 people.
Senior Director of Strategy, Veeva Clinical Operations
Senior Consultant and Services Lead, Continuous Innovation, Clinical Operations
Have questions about Boehringer Ingelheim’s data transformation journey? Stick around after the session for an informal chat with Martin Heckenberger and other experts from Boehringer Ingelheim’s One Medicine Platform (OMP) team.
Capability Owner Clinical Data Collection
Join the Clinical Data CTO for a visionary discussion. Learn three key areas of focus over the next 3 years, and give your feedback on each of them. This is a continuation of last year’s “next big ideas” discussion, which have since evolved into “big plans” to advance better science together.
Chief Technology Officer, Clinical Data
Explore how to automate global post-market case processing. Simplify intake of unstructured data, improve data quality with embedded configurable QC workflows, and use rule-based narrative generation.
Vice President Product Architect, Veeva Safety
Join us as we publish a Japanese eCTD 4.0 submission using Veeva Submissions Publishing and get an early preview of U.S. eCTD 4.0 forward compatibility – all within the same processes used today, without any add-ons.
Senior Product Manager, Submissions Publishing
Join us to hear about the key outputs from the latest Veeva Regulatory Community Meeting in Brussels where we discussed best practices for label management in Veeva RIM. Learn what actions Veeva is taking as a followup from the meeting and in support of the ePI Roadmap implementation.
Director Regulatory Strategy
Join the Veeva Business Consulting team to learn how to optimize your RIM implementation roadmap, taking into consideration technical feasibility, business value, change effort, and cost considerations to find the right path forward for your organization.
Regulatory Practice Lead, R&D Business Consulting
Discuss your experience of deploying Veeva Connections with industry peers. Share successes, challenges and the alue added. Veeva teams will also be available for feedback and guidance
Senior Manager, EU DevCloud Strategy
Explore process monitoring, a recent Vault Platform capability that identifies process bottlenecks and measures workflow KPIs to drive greater process efficiency
Senior Director or Product, Vault Platform
Engagement Manager, R&D Business Consulting
Explore the untapped potential of Data and AI within Veeva Vault, providing Accenture’s unique point of view on how organizations can further unlock business value beyond a standard implementation. From streamlining workflows to enhancing predictive analytics, we will dive into practical opportunities that can transform the way life sciences companies operate.
EU R&D Pharmacovigilance & Operations Lead
European Regulatory Lead
Hear how unification between Veeva LIMS and the Quality Cloud drives efficiency and compliance across Veeva QualityDocs, Veeva QMS, Veeva Training, and Veeva Batch Release.
Senior Director, Veeva LIMS Strategy
Solution Consultant, Veeva LIMS
Collaborate with CROs in real-time and get data oversight and greater control over safety outputs. Easily identify bottlenecks and track case quality and average handling times to improve operational efficiency.
Solution Engineer
See how Vault Action Layouts simplify the user experience by providing the right information at the right time for the right role and context.
Principal Product Expert, Vault Platform
ITM details how to provide study-specific training for internal and external staff in Veeva Study Training, streamlining training administration, reporting, and compliance.
Vice President, Head of Global Clinical Operations
GSK shares how it moved feasibility into Veeva Study Startup, replacing manual tools with standardized, technology-enabled processes. Learn how early engagement, data reuse, and process improvements are helping reduce site burden, improve data quality, and build stronger site relationships.
Strategy Product Owner – SSU
Learn how Novo Nordisk managed transformational changes and results during its first year of the Veeva Clinical Data journey. With ambitious goals and a strong program (DataNow), the team delivered efficiency and operational excellence. In a panel with Syneos Health Consulting, hear the strategy to redesign processes, structure change, adapt to challenges, and plan for the next phase of value.
Vice President
Implementation Manager
Senior Director, Strategy, Clinical Data
Director, Data Systems & Application
Discover insights into the strategic roadmapping approach that shifts quality management improvements from incremental changes to significant advancements, supporting both immediate and long-term business objectives.
Senior Manager
Join a global biotech company as they share their journey with Veeva LIMS. From selection to real-world results, hear about their implementation best practices, key improvements, and the impact on their QC operations.
Senior Project Lead
Learn how harmonizing quality systems standardizes operations across 14 facilities and creates consistency for customers. Hear how Veeva Quality Cloud streamlines processes and improves service to global markets.
Corporate eQMS Manager
Group IT QA Lead
Hear about organizational change management strategies that drive successful QMS harmonization across an enterprise. Learn actionable insights on how to foster user adoption and deliver maximum value through effective implementation.
Head of Corporate eQA Systems & IT Validation
Program Lead
MSD, Sandoz, and a top biopharma discuss their pharmacovigilance digital transformation strategy. Learn how an in-house unified safety data and content solution is enabling greater operational efficiency, higher-quality data, and improved decision-making.
Director, Patient Safety Data Operations and Analytics
Head Digital Strategy, Patient Safety Pharmacovigilance Operations
Director, Business System Management and Innovation
Director, Veeva Safety Strategy
Achieving full value of Veeva RIM requires strategic feature adoption and seamless deployment. Learn AstraZeneca’s best practices for leveraging new capabilities to enhance regulatory efficiency, ensure compliance, drive continuous improvement, and respond to user feedback.
Senior Director, Regulatory Information Systems
Enterprise Regulatory Vault Product Manager
Director, IT, Global Delivery, Regulatory & QA Platform
Maximizing the value of your Veeva RIM investment requires effective change management and training. Join Chiesi and Veeva Business Consulting as they share insights and best practices for optimizing adoption.
Head of Global Regulatory Affairs Digital and Publishing
Regulatory Practice Lead, R&D Business Consulting
See how Karo Healthcare leverages Vault Reporting and Dashboards, including new process reporting and KPIs, to drive operational improvements, mitigate risks, and better allocate resources. Get a sneak peek into the roadmap and upcoming capabilities.
Senior Director or Product, Vault Platform
Product Quality Manager / Process owner Deviations
Director Operations ECM
Boehringer Ingelheim shares their successes, lessons learned, and the value of implementing four vaults in parallel. Get an inside look at how they optimized to decrease cycle times and increase data accessibility.
Head of ClinDev Operations Capabilities
Head of Global Regulatory Operations & RA Digital Innovation
Executive Director – Program Manager One Medicine Platform
Head Learning, Processes & Digitalization
Thursday, 5 June
Sanofi shares its approach to streamlining study training by implementing Veeva Study Training as a single, inspection-ready solution. The team discusses how to eliminate the need for multiple disconnected systems across study teams and site staff.
Transformation Catalyst
Digital Product Line Owner
Recordati shares the transformation journey to bring key clinical operations systems in-house with CROs working in its systems. Learn why change was needed, how the company evaluated new applications, and how Veeva Clinical Operations is helping improve oversight and quality.
Group R&D Digital Solutions Manager
Hear industry leaders from UCB, Boehringer Ingelheim, Vitaflo, and Allucent share their vision to raise the standards of eCOA delivery. The discussion will address the challenges that increased adoption presents for sites and study teams. Discover practical strategies to expand use without adding workload and hear real-world examples of successful implementation.
SVP Product Management, Sites and Patients
Capability Manager
Global Head Patient Engagement
Chief Digital Technology Officer
Global Clinical Data and Biometrics Manager
Explore how a collaborative partnership is laying the foundation for the lab digital core—a connected ecosystem that integrates Veeva LIMS with lab instruments to improve productivity and compliance, setting the stage for labs to harness AI and advanced analytics to drive scientific discovery.
Chief Technology Officer
Hear Veeva’s vision and roadmap to enable faster, more confident GMP release and market-ship decisions with Batch Release.
Director of Batch Release Strategy
Sr. Director of Product Management
Learn why adopting an integrated quality management approach creates a strong foundation for digital transformation. Discover how Bayer consolidated their fragmented legacy system landscape to drive efficiency and progress in their strategic journey towards predictive quality.
Lead Digital Quality
S&T Senior Project Manager
IT Program Lead
Gain perspectives in a panel discussion exploring balancing GxP training compliance requirements with the growing emphasis on a more consumer-centric approach to learning.
Documentation and Training Global Manager
Associate Director, Process and Training Management
Vault Quality Product Manager
Director, Training Strategy
Novo Nordisk shares how it is streamlining operations with one global safety solution and driving efficiencies by connecting safety across the enterprise.
Senior Director, Safety Operations Office & PV Technology
Learn how Submission Content Plans and high data quality are enhancing decision-making and capacity management for regulatory operations in a small biopharma company.
Regulatory Operations Team Lead
Regulatory Practice Lead, R&D Business Consulting
Explore Veeva’s strategy to help customers speed submissions with multi-health authority collaboration platforms. Boehringer Ingelheim will cover Project PRISM’s regulatory cloud and advanced analytics initiative, while Accumulus will demonstrate its regulatory collaboration, current pilots, and future opportunities.
Senior Director, Government Strategy
Vice President, Global Regulatory Intelligence & Policy
Senior Vice President Regulatory Innovation
Hear how Haleon is managing and maintaining five Vaults and optimizing the release process across these environments. Get an overview of its approach to simplify configuration management and automate deployment.
Senior System Engineer, R&D Safety
QSC System Technology Manager
Senior Director, Development Cloud Strategy
Hear how Sanofi is leveraging Direct Data API to drive business value and enhance decision-making. Discover how to seamlessly export Vault data into data lakes / warehouses for advanced analytics and reporting and practical applications across product development.
Director of Product Management, Developer Experience
Technical Engineering Expert
See how Veeva Clinical Operations improves study partnerships by streamlining document exchange and safety letter distribution, automating training, and reducing administrative burden.
Solution Consultant
Learn how two of the newest CDB features enable data managers to work more effectively. See how Observations lets data managers collectively evaluate data points before creating queries, and how the Query Metrics Dashboard helps them prioritize the most critical queries to action.
Senior Manager, North American Solution Consulting, Clinical Data
Learn how others are leveraging modern eCOA data management approaches in study design and management. Discussion topics include practical examples of successful data capture, flow, and analysis, including connections with CDB, to increase data quality and integrity.
Senior Director, eCOA Strategy
SVP Product Management, Sites and Patients
Explore the updated ICH E6(R3) guidelines and their impact on clinical data management. Discuss the new data governance section alongside topics such as database decommissioning and signature dueness. Exchange insights, review best practices, and ideate on the arising industry challenges.
Director, Product Expert, Clinical
Director, Clinical Strategy
Hear how a connected safety platform seamlessly automates adverse event (AE) intake from medical information, product quality complaints (PQCs), and clinical subject reportable events. Learn how connections with Veeva EDC, QMS, and MedInquiry streamline case intake, reduce reconciliation, and improve efficiency.
Senior Solution Consultant
Approach and ways to leverage Github to automate deployment of new releases.
Veeva Product & Platform Architect
Senior System Engineer
Sr. System Engineer
Implement advanced conditional logic with configuration in Vault. Reduce dependency on custom code for the automation of steps in business processes.
Senior Product Expect, Vault Platform
Learn how to facilitate accurate batch release and product lifecycle management with Active Dossier by maintaining a list of current documents for a given product in multiple markets.
Solution Consultant, Regulatory
Explore key Veeva Publishing value drivers and learn to effecitvely leverage them for a strong business case for implementation.
Senior Director, Regulatory Strategy
See a preview of the new quick queries feature, releasing this year, and how it will create significant time savings for sites and CRAs. Use standard phrases to create or resolve queries with a single click. This new and innovative capability automates query authoring and responses, saving organizations hours of time and effort.
Principal Solution Consultant
Explore the new capability of jurisdictional control to automate the release of batches based on market approval updates.
Director of Batch Release Strategy
Explore how to automate global post-market case processing. Simplify intake of unstructured data, improve data quality with embedded configurable QC workflows, and use rule-based narrative generation.
Vice President Product Architect, Veeva Safety
Explore how real-time data sharing and connected workflows between Clinical Operations and Vault CRM can strengthen site relationships and speed clinical trial execution.
Senior Product Manager, Clinical Operations
Bayer has executed a unified clinical strategy that involves early adoption of many Veeva Clinical Platform applications. Join Bayer to hear insights from its multi-year “Gemstone” program, which has driven significant simplification, including the decommissioning of over 30 applications and 80 integrations.
Head of Clinical Trial Management Services and Solutions
Senior Vice President, Clinical Strategy
Dompé and Excelya discuss how CROs can work effectively in a sponsor-owned eTMF. Learn how this approach improves sponsor oversight and efficiency while leveraging CRO expertise.
International Business Director
Clinical Development Methodology Director
Discover how connection-driven automation accelerates trials, benefiting patients, sites, and sponsors. See a live demo of examples spanning study build, AI-driven coding, and data exports. Learn how one biopharma drove success and innovation.
Senior Director, Clinical Data Strategy
Principal Solution Consultant
Hear how Quality Intake in Veeva QMS ensures that only relevant supplier events are initiated as Quality Events. Learn how the controlled intake process streamlines the registration, assessment, and retrieval of cases, providing full oversight and efficient management.
Senior Manager
Explore a game-changing approach to data migration for Veeva LIMS with a powerful integration solution that simplifies data import. Learn how to seamlessly migrate data from any source, accelerating implementation, reducing resource needs, and minimizing disruption.
Global Account Partner
Vice President – Service Delivery
Explore how modern, unified quality systems can enhance customer service and improve quality within CDMO operations. Learn from Richter Biologics’ experience in expanding their quality ecosystem to drive greater value and collaboration with their customers.
Teamlead GMP Compliance
Explore how a biotech company scaled its quality system to support rapid growth from start up to global operations. Gain insights into challenges faced, strategies applied and lessons learned on building a robust, scalable quality framework.
Senior Director Global Systems Quality
Learn how Chiesi simplified PSMF management by harmonizing processes and supporting seamless collaboration across internal/external content owners and reviewers. Hear how they improved global oversight, maintained inspection readiness, and enabled regional teams to produce a complete PSMF in a simple and fast way.
Global Pharmacovigilance Digital Innovation & Technologies Manager
Regulatory affairs has become a data-driven operation, requiring enhanced automation and streamlined processes to leverage data from multiple sources, improving submission quality and speed. Learn how Gedeon Richter uses Veeva RIM to drive efficiency across the entire RIM process – enabling growth and innovation.
Global Head Regulatory Science Strategy & Operation
A Master Data Management system is key for a long-term data strategy and robust cross-functional technology infrastructure. Learn Novartis’ experience building an MDM system to seamlessly integrate product data into Veeva RIM.
Head, Data Strategy & Management
RA CMC Senior Manager Data & Digital
Engagement Manager
Explore how to extend Vault through advanced configuration and customization with real-world examples. Learn how to create custom data objects, tailor the user interface, connect with external systems to automate business processes.
Vice President of Product Management, Vault Platform
Director of Product Management, Vault Platform
OM Pharma outlines its governance approach to harmonizing six Veeva Vault applications across three business areas. Aiming to improve operational efficiency and agility, the digital journey will evolve GxP systems to enhance connectivity among development data, proactively manage the business, and facilitate better decision-making through deeper insights. By breaking down silos and fostering a data-driven mindset, the company aspires to build a cohesive infrastructure that supports growth and innovation.
IT Application Manager
See how to use existing data and documents from Veeva Clinical Operations, including TMF documents, to automate sponsor, CRO, and site training in Veeva Study Training. Then, automatically file evidence of training completion in Veeva eTMF to increase compliance.
Senior Solution Consultant
Learn how Veeva eCOA simplifies the design, management, and completion of clinical outcome assessments for sponsors, sites, and patients.
Senior Solution Consultant
Hear practical examples of how companies are accelerating clinical trials with connections like EHR to EDC, the Study Design API, and Study File Format. Explore current and future applications while gaining ideas for how to leverage connections in your own organization.
Senior Vice President of Product, Clinical Data
See how a unified safety solution accelerates data flow for earlier signal detection and aggregate reporting, links signals back to source case data, supports more detailed analysis, and streamlines RMPs and aRMMS based on signal outcomes.
Principal Product Manager, Veeva AI (Safety)
Senior Product Expert, Veeva Safety
Join us to learn how BASE Life Science’s GAIA platform transforms RIM operations by leveraging domain-specific AI Agents tailored to key business processes within Regulatory Affairs. We will demonstrate how GAIA seamlessly integrates with Veeva RIM to reduce manual effort, shorten review cycles, minimize human error, and focus on higher-value work.
Head of AI & Automation
See how Sponsors and CROs can automate the safety letter distribution process, as well as improve site acknowledgment tracking and oversight, driven by Veeva Connections across EDC, Safety, CTMS, Site Connect, and SiteVault.
Senior Solution Consultant
Senior Director, Development Cloud Strategy
Learn how AI, alone or paired with human linguistic expertise, can elevate your translation and localization strategy. See an overview and customer case study of how the GlobalLink AI platform integrates with Veeva QualityDocs for seamless, efficient translations across global markets
Director, AI Consulting
See how the latest updates in Veeva Study Training further streamline training. Learn how to automate training assignments based on responsibilities, increase CRA visibility with the My Study Team page, and exempt PIs from duplicate training.
Solution Consultant, Clinical Operations
See how the seamless connection between RTSM and EDC automates data transfer to reduce the risk of errors from manual transcription, eliminate duplicate data entry for sites, and reduce data review and reconciliation efforts for data managers.
Solution Consultant, Clinical Data
Discover how process reporting can be leveraged across the organization to measure operational health and efficiency
Senior Director, Veeva Regulatory Strategy
See the latest best practices for Veeva Governance and how a Center of Excellence can help drive cross-functional collaboration across multiple Vaults.
Senior Director, Development Cloud Strategy
Get the latest updates on Station Manager with a live demo of real manufacturing use cases. Learn how it drives productivity and enhances compliance on the shop floor.
Senior Product Expert
Strategy Director, Quality & Manufacturing
Hear how Veeva Disclosures leverages automation and unified systems to improve compliance, accelerate submissions, and further simplify disclosures with new features released in 25R2.
Solution Consultant
In this session for Veeva eTMF customers only, you’ll learn about risk-based approaches for TMF management and features you can use to create additional efficiencies.
Product Expert, Clinical Operations
Senior Director, Clinical Strategy
Join this session to discuss the assessment and documentation of decision-making throughout a trial, in alignment with the latest ICH E6 (R3) guidelines. Share insights on current processes and opportunities for improvement. Open to Veeva CTMS customers only.
Senior Product Expert, Clinical Operations
Senior Director of Strategy, Veeva Clinical Operations
Discuss best practices for end-to-end clinical processes, such as monitoring, SDV, payments, and protocol deviations. See what it means to have a single source of truth across clinical operations and clinical data. Plus, give feedback on early ideas to optimize the CRA experience and improve ways of working across the study team.
Senior Director, Strategy
Hear CROs and sponsors speak to their best practices for change management to own their own data. See how they access data and govern activities on their terms. Learn about process standardization, CRF efficiency, technology considerations, and the ideal operating model for streamlined study delivery.
Learn how Veeva Validation Management improves the efficiency and traceability of equipment qualification activities.
Director, Veeva Validation Management Europe
Senior Solution Consultant, Validation Management
Join this session to share best practices, hear from product experts, and discuss latest and upcoming capabilities. Open to Veeva Safety customers only.
Sr. Director Veeva Safety – Europe
Get the latest updates on EMA’s PMS activities and roadmaps, including insights from a customer’s current PMS Pilot preparations. Learn how an IDMP Ontology project at Pistoia Alliance is advancing semantic interoperability, based on FAIR principles, to enhance existing IDMP standards
Vice President Regulatory, Europe
Master Data Manager
Senior Consultant, Veeva RIM
eCTD 4.0 roll out is starting. Join us to learn about the enhancements and benefits eCTD4.0 brings and how to prepare.
Director Regulatory Strategy
Senior Product Manager, Submissions Publishing
Discover open-source tools, built using Vault API, that increase administrator and developer productivity with an intuitive user interface.
Senior Product Expect, Vault Platform
Director of Product Management, Developer Experience
Discover change management best practices and recommendations for multi-Vault implementations and landscapes to sustain user adoption and satisfaction. See how change management enables key cross-functional processes.
Engagement Manager, R&D Business Consulting
Get a preview of Veeva AI and Agent use cases in the Development Cloud and Quality Cloud applications. Understand how AI in the platform and embedded into applications will enable broad adoption to help users analyze data, draft documents, and extract information out of unstructured content.
SVP, Veeva AI Solutions
See how TMF Transfer and CTMS Transfer automate information and document exchange between sponsors and CROs, driving improved oversight, visibility, and compliance.
Senior Solution Consultant
Learn how to access the raw text extracted from your documents after they are uploaded to Vault. This unformatted text can be sent to LLM’s and Gen AI services with the need to export source files from Vault.
Director of Product
Clinical trials offer patients vital access to new therapies, with research sites serving as the primary point of contact for treatment and data collection. This keynote will discuss strategies to reduce the burden on site staff, improving efficiency and study quality for the benefit of sites, sponsors, and ultimately, patients.