#RBQMLive

RBQMLive 2025 On-Demand

Keynote—Measuring the Impact: Quantifying the ROI of RBQM

Speakers: Ken Getz, Executive Director & Professor, Tufts CSDD; Abby Dirks, Data Scientist, Tufts CSDD
  • Evaluate ROI using NPV analysis to quantify financial and operational impact
  • Review the latest data modeling research with real-world data and case studies
  • Explore how RBQM aligns with ICH E6(R3) guidelines to improve clinical trials
  • Discover measurable benefits of RBQM, making a strong case for adoption
  • Get actionable strategies for integrating RBQM into clinical trial operations

Panel—Decoding ICH E6(R3): From Principles to Practice

Participants: Cris McDavid, Senior Director, Global Clinical Operations, Parexel; Dawn Anderson, Managing Director, Life Sciences Clinical Transformation Leader, Deloitte; Leonie Christianson, Business Consultant, Syneos Health
  • Understand updated ICH E6(R3) guidelines and their impact on trial oversight
  • Hear how Sponsors and CROs are adapting quality systems to the guidelines
  • See how RBQM and integrated data review improve data quality and reduce risk
  • Discover practical approaches with change management and digital tools
  • Learn how Sponsors, CROs, and regulators are collaborating to meet evolving expectations

Harnessing AI for Risk Based EVERYTHING: Current Innovations & Future Directions

Speaker: Drew Garty, Chief Technology Officer, Veeva
  • Explore how AI improves protocol design, risk identification, and trial efficiency
  • Learn from case studies showcasing AI-driven RBQM in practice
  • Manage the shift to AI-powered RBQM with engagement and training
  • Gain a forward-looking view of how to prepare for upcoming innovations and methodologies
That’s a Wrap!
All three sessions are available on demand and ready to watch, revisit, save, or share.