Clinical Study Data Flow Maps 

A practical guide for trial sponsors on navigating data integrity, traceability, and sponsor oversight in the ICH E6(R3) era.

This webinar explores how Clinical Study Data Flow Maps can help sponsors build a clear, defensible understanding of their data ecosystem. Participants will learn practical approaches for defining scope, identifying critical data pathways, establishing ownership, and developing data flow maps that support oversight, traceability, and inspection readiness.

What You'll Learn

• Why Clinical Study Data Flow Maps are receiving increased regulatory attention
• How to determine what should and should not be included in your map
• How to identify critical systems, vendors, and data transfer pathways across the study lifecycle
• What level of detail supports traceability without creating unnecessary complexity
• How to establish ownership, governance, and maintenance responsibilities
• How to use data flow maps to support sponsor oversight and inspection readiness

• Live participation in the 90-minute live webinar on Clinical Study Data Flow Maps
  • Includes expert presentation, moderated panel discussion, and live Q&A
• Insight from anonymized participant data showing how sponsors compare across confidence, experience, and approaches
• 30-day access to the on-demand recording (presentation and panel discussion; live Q&A excluded)
• Clinical Study Data Flow Mapping Starter Kit, a practical guidance, worksheets, and implementation tool for trial sponsors, sent post webinar
• Presentation Slides from the webinar, sent post webinar