10 – 12 November, 2025

Agenda

Monday, 10 November
17:30 CET
Registration Opens

18:00 CET
Cocktails / Refreshments

18:45 — 21:00 CET
Welcome Reception Dinner

Tuesday, 11 November
7:30 — 8:30 CET
Networking Breakfast

8:10 — 8:30 CET
See how Veeva and Redica are teaming up to bring regulatory intelligence to the Veeva RIM Platform with a live demo.

8:45 — 9:45 CET
Opening Keynote

10:00 — 11:00 CET
Learn how a well-executed digital transformation accelerates clinical discovery, produces measurable results, and delivers significant business value by better conncecting sites, patients, and sponsors.
Hear insights into a regulatory transformation journey, including guiding principles for successful RIM implementation, step-by-step approach, and strategies to ensure effective system deployment and user adoption.
Top-down quality transformations often face a critical challenge: striking a balance between standardizing processes, systems, and people, while simultaneously preserving the unique operational needs of diverse divisions, sites, and geographies. Learn best practices from quality leaders who have successfully steered large-scale transformations within complex global organizations, revealing how they achieved consistency without compromising agility.
Whether you're in marketing or part of the medical, legal, regulatory (MLR) review, learn how intelligent agents streamline MLR workflows, lighten reviewer load, and enable faster, smarter content delivery.
CMOs share best practices and real-world case studies for positioning and integrating medical affairs across the organization to drive business impact and maximum influence.

11:00 — 11:45 CET
Connect Break / Refreshments

11:20 — 11:40 CET
Learn how large language models are driving MLR efficiency with upstream quality checks and seamless content review with MLR Bot.

11:45 — 12:30 CET
Learn how a unified clinical ecosystem seamlessly connects patients, sites, and sponsors. This end-to-end demo showcases how to simplify and standardize across clinical operations, EDC, CDB, eCOA and Image management.
Maintaining a product portfolio under the demands of MDR and IVDR requires continuous effort. By optimizing PMS data collection and analysis, companies can shorten core processes and product re-certification timelines. Learn how to transform PMS from a compliance activity into a strategic accelerator; including the role PMS can play in international reliance and speed to market.
Commercial and medical teams are essential touchpoints in the customer journey, but too often operate in silos. Explore how aligning communications across PromoMats and Veeva Medical Suite ensures one voice to the market, enables a 360° view of content, interactions, and insights across sales, marketing, and medical teams.
Learn how Medical Safety directly impacts patient outcomes and business success and how it integrates with other functions, including approaches for building a robust Medical Affairs strategy.
Strategic AI: Evaluating and Preparing Business for the Future
Tech & Transformation Session

12:45 — 13:30 CET
Explore best practices for digitalizing clinical data management, including change management strategies for successful implementation and user adoption.
Experts from notified bodies discuss the current state and the future of electronic regulatory submissions, including trends, potential challenges, and evolving compliance expectations.
Dive into the art of the possible for modernizing the entire quality organization with integrated QMS, smart data use, and emerging technologies to transform cumbersome processes into a dynamic, scalable operation. Explore practical pathways to agility, compliance, competitive advantage, and quality innovation.
Discover effective strategies for content localization that drive faster approvals, minimize errors, and deliver stronger market impact, while preserving compliance.
Uncover the critical role of Key Opinion Leader (KOL) partnerships in fueling innovation and rapid product adoption. Learn how to unify KOL management to streamline processes for more impactful relationships.
Learn how the Vault Platform is evolving to support medtech customers across all domains. We'll review recent highlights around user productivity and scalability along with cross-functional connections to maximize value.

13:30 — 14:45 CET
Networking Lunch

14:20 — 14:40 CET
Understand how to implement workflows to streamline approvals, reduce reviewer workload, and achieve faster time-to-market with a tier-based review model

14:45 — 15:30 CET
The Veeva Clinical team will cover recent releases and new features planned for the upcoming year. Learn about new features across the Veeva Clinical Platform.
Hear about the most recent and upcoming Veeva RIM features across Registrations, Submissions, Publishing, and Archive, as well as a detailed roadmap for optimizing the overall Veeva RIM experience.
Discover strategies for driving success with a holistic approach to the adoption of the Veeva Quality Cloud, including how partnership, communication, and prioritization contributes to ongoing success.
Commercial and medical teams are essential touchpoints in the customer journey, but too often operate in silos. Explore how aligning communications across PromoMats and Veeva Medical Suite ensures one voice to the market, enables a 360° view of content, interactions, and insights across sales, marketing, and medical teams.
Improve your organization's visibility into operational processes, application usage, and KPIs with Vault reports and dashboards. Learn about Vault reporting's core tools and how to use them to convert an idea for a metric into an actionable dashboard.

15:45 — 16:30 CET
Learn how to implement a compliant-by-design eTMF system, including the key drivers for change, strategies used to manage the transition while maintaining daily operations, and methods used to define, measure, and deliver tangible business value.
Elevate your organization by transforming claims from a compliance hurdle into a powerful competitive advantage. Discover how a shared claims foundation accelerates content delivery, strengthens compliance, and prepares your organization for AI and global expansion.
Hear about the most recent and upcoming Veeva Quality Cloud features across QualityDocs, QMS, and Training, as well as a detailed roadmap for optimizing the overall Veeva Quality experience.

16:30 — 17:15 CET
Connect Break / Refreshments

16:35 — 16:55 CET
See how medtechs can unify image management with Veeva EDC

18:30 — 22:30 CET
Evening Event (Off Property)

Wednesday, 12 November
8:00 — 9:00 CET
Networking Breakfast

8:30 — 8:50 CET
See how validation management streamlines commissioning, qualification, and validation across systems, equipment, and processes

9:00 — 9:45 CET
Hear the business drivers and best practices for moving from an outsourced model to running trials in-house including technology, people, and processes that need to change to ensure clinical success and strong CRO collaboration.
Learn how Cytiva approached system validation, user engagement, and change management for a global implementation of Veeva Submissions and Submissions Archive. They will offer guiding principles and actionable strategies to help others ensure effective system deployment and user adoption for future RIM projects.
Discover how real-world innovations and developing industry best practices around AI are driving quality improvements. Learn how strategic alignment, technology adoption, and practical applications deliver greater efficiency and innovation.
See the latest Vault PromoMats content innovations to simplify the user experience, increase speed, and enable reuse with modular content.
Learn about the Veeva Medical Suite, including Link Key People from the Veeva Medical team, as well as recent releases and new features planned for the upcoming year.
Hear how leading medtech companies are unlocking value through operational tactics like business case definition and ongoing value realization projects. We'll also review how to prioritize strategic business objectives within your technology transformation roadmap.

10:00 — 10:45 CET
Unifying E2E Clinical Evidence Strategy
Clinical/Medical Session
Generative AI and large language models have the power to revolutionize the medtech industry. Discover various AI applications from regulatory affairs to marketing, sharing insights from initial pilots, and leveraging lessons learned from broader industry journeys to inform future adoption.
In the highly regulated medtech industry, traditional silos between quality assurance and R&D can create compliance risks and hinder speed to market. Learn how leading medtechs are bridging this divide with strategies to integrate quality directly into the design and development lifecycle through the connection of PLM and QMS processes. This deep integration empowers quality operations with enhanced visibility and proactive control, while providing engineering with streamlined workflows and direct access to essential quality data.

10:45 — 11:30 CET
Connect Break / Refreshments

11:00 — 11:20 CET
Streamline processes and access deeper data to drive meaningful KOL engagement

11:30 — 12:15 CET
Closing Keynote

12:15 — 13:30 CET
Networking Lunch

13:00 — 13:20 CET
Learn how to speed approvals and ensure accuracy of scientific communications and inquiries.

13:30 — 15:30 CET
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.
Explore how regulatory intelligence programs streamline key information. Discover use cases for optimizing these programs and learn tips to drive greater business value. We'll also showcase Veeva RIM's regulatory intelligence offering, supported by strong evidence from pilot programs and external validation.
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.

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Madrid | Monday, 10 - Wednesday, 12 Nov, 2025

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