Agenda Overview
Monday, 2 November
Tuesday, 3 November
Transform clinical evidence form a regulatory requirement to a strategic tool by integrating real-world evidence data across the product lifecycle to accelerate market access.
Transform the complex EU MDR/IVDR overhaul into a strategic advantage. Industry experts share how syncing cross-functional data turns periodic re-certifications into a streamlined model of agile, continuous compliance.
Learn how embedding Veeva AI into PromoMats workflows accelerates content velocity, improves asset quality, and supports compliant review and approval processes. Discover practical strategies for driving adoption and scaling AI across the content lifecycle.
Chief Medical Officers share strategies for transforming the medical function into a core business driver. Discover how to break down legacy silos and leverage data-driven strategies to drive growth and enterprise-level objectives.
Breakdown geographic silos and drive continuous improvement by leveraging the Vault Clinical Platform and harmonizing processes.
Get a blueprint for successful RIM implementation including goal and metric definition, multi-year roadmap planning, and change management; regardless of company size.
Transform post-market surveillance by breaking down the walls between complaint handling, CAPAs, and downstream processes to accelerate root-cause analysis, drive traceability, and ensure audit readiness.
Discover how leading medtechs are preparing for the future of commercial excellence. Hear how they are thinking about AI, evolving business models, and strategic priorities to position their organizations for long-term success in a rapidly changing market.
Learn from medical affairs innovators as they share their playbooks and industry benchmarks for building a digital infrastructure that measures organizational impact and gains leadership credibility.
Get a practical framework to modernize your clinical operations with key benchmarks for efficiency, compliance, and realized value.
Get up to speed on the latest EUDAMED timelines and regulatory requirements, including insights to comply with new UDI regulations.
Rethink quality and product innovaton with risk-based decisioning to streamline systems and processes, maintain continuous compliance, and deliver greater value to patients.
Building a scalable foundation for claims management by creating a single source of truth for claims and standardized MLR processes to accelerate time-to-market and mitigate compliance risk.
Scaling modern medtech Medical Affairs requires breaking down critical operational roadblocks. Explore how to solve these friction points by blending agile cross-functional processes with targeted technology.
Create the foundation for effective site relationships that enables digital collaboration, higher efficiency, improved compliance and oversight .
See the latest and upcoming Veeva RIM innovations across Registrations, Submissions, Publishing, and Veeva AI.
Transform daily operations with a flexible, fit-for-purpose quality landscape that eliminates data silos and drives lasting competitive advantage.
Learn how robust program governance aligns clinical, regulatory, and commercial priorities to ensure your tech transformation drives maximum value across the product lifecycle.
Transform routine medical inquiry data into a powerhouse of actionable scientific intelligence with purpose-built digital infrastructure. Learn how deep field insights build strategic credibility that can influence future R&D, clinical development, and commercial strategies.
Transitioin from a fragmented, CRO-led clinical approach to a unified in-house operating model to drive trial speed, data contral, and real-time oversight.
Discover how AI agents are redefining regulatory operations by automating heavy workloads and supporting critical decisions, including how Vault AI for promotional reviews and regulatory submissions strengthens compliance, accelerate time-to-market, and maximizes productivity.
Hear about the most recent and upcoming Veeva Quality Cloud features across QualityDocs, QMS, and Training, alongside new AI and platform innovations optimizing the user experience.
See the latest PromoMats innovations to simplify the user experience, increase efficiency, and improve traceability through the lifecycle of promotional content.
Break down how the rise of AI tools changes how clinicians find and consume scientific data. Learn how these shifting user habits can impact omnichannel stakeholder engagement, information dissemination, and the future of medical communications.
Wednesday, 4 November
Insights into how clinical evidence requirements are shaping digital transformations, long-term clinical strategies, organizational structures and business objectives.
Regulators and industry experts share current and future of electronic regulatory submissions, including trends, pitfalls, and evolving compliance expectations.
Move from a compliance-driven operations to an innovation engine led by a culture of quality. Learn how cross-functional collaboration and standardization ensure a patient-centric focus.
Modern medtech purchasing decisions involve multiple stakeholders, requiring precise and compliant commercial alignment. See how a leading medtech masters the end-to-end buyer journey to deliver impactful, tailored customer experiences.
Compliantly bypass local entry barriers by leveraging precision expert mapping and cross-border institutional alliances. Get actionable frameworks to align global scientific leaders and accelerate international commercial adoption.
Hear the newly released and planned capabilities across Veeva Vault Clinical Platform.
Customization an perpetuate broken workflows, but standardization helps maintain clean data architeccture, faster launch
Eliminate bottlenecks, improve data integrity, and reduce cycle times with digital validation management.
Disconnected commercial tools lead to wasted marketing investments and missed insights. Explore how to bridge the gap between content creation and field execution to deliver seamless, compliant interactions and fuel a continuous data feedback loop.
See how the Veeva Medical Suite advances each step of the Medical Affairs lifecycle, including key medical responsibilities across stakeholder identification, scientific exchange, and inquiry management to show how a unified digital ecosystem drives efficiency and deep clinical insights.
Collaborate with your peers and Veeva experts during an open discussion on clinical best practices and how to leverage Veeva Clinical applications to drive efficiency. We'll also dive into the latest features.
Collaborate with your peers and Veeva experts during an open discussion on regulatory intelligence, efficiency, and compliance. We'll also dive into the latest features of Veeva RIM.
Collaborate with your peers and Veeva experts during an open discussion on quality best practices and how to leverage Quality applications to drive efficiency and safety. We'll also dive into the latest features of the Quality Platform.
Collaborate with your peers and Veeva experts during an open discussion on commercial and claims management best practices and how to leverage Commercial Content applications to drive efficiency, compliance, and speed to market. We'll also dive into the latest features.
Collaborate with your peers and Veeva experts during an open discussion on medical affairs best practices and how to leverage Medical applications to drive efficiency. We'll also dive into the latest features.