Biopharma brands rely on static websites and email to engage patients and HCPs, yet these channels often function as one-way communications that make it difficult for users to quickly find the information they need.
Join this session to learn how leading brands are transforming existing MLR-approved content into compliant, conversational AI experiences that deliver instant answers and generate commercial evidence to improve engagement and content strategy.
Topics include:
- Why static brand.com and one-way email playbooks fail patients and HCPs
- How conversational AI drives a 7x lift in high-value actions to advance treatment
- Best practices for MLR-approval and implementation
- Generating actionable commercial evidence to optimize your content strategy
Speakers:
- Ahmed Elsayyad, President, Veeva Ostro
- Gregory Le Cleir, Head of Uro Oncology Patient Marketing, Ferring Pharmaceuticals
Veeva AI for Regulatory is positioned to enable agentic regulatory. It includes purpose-built solutions that solve key regulatory challenges, increasing efficiency and speed, and giving you more time to focus on strategic work.
Join this session to learn how Veeva AI brings AI capabilities to Veeva RIM to automate and simplify work, while maintaining security and compliance for regulated environments.
Solutions featured in the session:
- Vault AI (Assistive AI): Delivers regulatory experiential insights and end user guidance in a new conversational way, helping users complete their work more efficiently.
- Veeva Falcon RIM (Agentic Labor): Standard agents that complete labor-intensive tasks, freeing time to focus on meaningful work like proactive submission planning and optimal dossier strategy.
- Veeva Falcon Writer (Agentic Authoring™): Generates submittable document drafts, working natively with Veeva RIM and Microsoft Word and dramatically reducing authoring cycle times.
Speakers:
- Pratyusha Pallavi, Executive Director, Falcon Regulatory
- Jordan Williams, Senior Product Manager, Falcon Regulatory
- Jonathan Gaynor, Senior Solution Consultant, Regulatory
- Cindy Ling, Senior Product Manager, Vault AI for Regulatory
Through scientific exchange, medical affairs teams gather critical voice-of-customer insights that uncover key opportunities to impact patient care. Veeva’s Agentic Insight Quality elevates this intelligence by coaching field teams to record rich, complete, and compliant entries directly within Medical CRM. The result is standardized, deep-context data that reduces discarded field notes by up to 70% and turns clinical insights into faster strategic action.
Join us for a live discussion and Q&A to learn how biopharma leaders elevate the quality and value of medical insights.
During the session, you will:
- See a live demo on how to provide real-time feedback to improve medical insight capture
- Discover how to configure guidelines tailored to organization-specific standards
- Learn how top biopharmas successfully bridge the gap between external clinical evidence and scientific strategy
Veeva Hosts:
Allie Reynolds, VP, Vault Medical StrategyTabby Miller, Senior Product Manager, Vault CRM
Annie Geraghty, Principal, Commercial Business Consulting
As AI adoption grows across the organization, monitoring agents and LLM token usage becomes important to scaling AI while maintaining control. Vault AI provides built-in monitoring and administrative tools to help organizations understand usage patterns, manage token consumption, and optimize AI operations—all within the Vault Platform.
Join experts to see:
- AI usage metrics, including AI actions, token consumption, execution time, and trends
- Live demonstration of built-in dashboards for usage monitoring and token alerts
- How to enable and disable users, agents and actions to ensure the right users have access to the right agents
- Q&A with Vault AI experts
Speakers:
Pat McQueen, CTO and SVP Solution Consulting
Andy Han, SVP, Vault AI and Vault Platform
Jared Katz, Senior Director, Development Cloud Strategy
Peter Delahaye, Senior Manager, Solution Consulting, Veeva AI
Clinical Research Associates (CRAs) manage site visits, documentation, issue follow-up, and study coordination. As administrative work grows, quickly finding information and prioritizing daily activities is increasingly critical.
In this session, we will demonstrate how Vault AI supports the full CRA workflow within Veeva CTMS. You’ll see how current AI capabilities—including the AI Tab, Record Chat, and Document Chat—help CRAs prepare for site visits, access study information faster, and accelerate visit reporting. We will also preview upcoming AI application agents and how they will further streamline clinical monitoring workflows.
In this session, you’ll learn how to:
- Prepare for site visits by quickly locating critical study and site information
- Prioritize non-visit work and reduce administrative effort throughout the monitoring process
- Use Vault AI capabilities to assist with reporting and targeted questions
- Explore the next generation of AI application agents planned for Veeva CTMS
Veeva Hosts:
Henry Galio, VP, CTMS StrategyKyle Stephenson, Director of Product Management, Clinical Operations
Kayla Mujkanovic, Senior Product Manager, Clinical Operations and MedTech
AI introduces additional validation considerations for GxP-regulated environments. Vault AI builds on the infrastructure qualification (IQ) and operational qualification (OQ) as part of the Vault platform, and is now complemented by agent evaluations and new monitoring tools.
Join experts for a live discussion and Q&A about:
- How Vault AI builds on the IQ/OQ-validated deterministic software foundation
- Veeva delivered Agent Scorecards to evaluate probabilistic outputs
- Ongoing Veeva agent monitoring to support continued performance and compliance
- Human-in-the-loop design principles
- Agent monitoring tools available natively in Vault Platform
Speakers:
Pat McQueen, CTO and SVP Solution Consulting
Andy Han, SVP, Vault AI and Vault Platform
Jared Katz, Senior Director, Development Cloud Strategy