[Webinar] Understanding the ISF Reference Model V1 Provisional and Its Impact on Sites

What if your ISF could be fully standardized, structured, and audit-ready?

As clinical trials become increasingly complex, maintaining clear, consistent, and compliant documentation is a growing challenge for clinical teams.

This on-demand webinar gives you the keys to better understand and adopt the ISF Reference Model, and to strengthen the quality and standardization of your study documentation.

What you’ll learn

In this session, our experts cover:

• The structure and objectives of the ISF Reference Model
• How to improve standardization and compliance of your study documentation
• Best practices to align your processes with emerging industry standards

Expert insights from CDISC

This webinar features contributions from CDISC experts, who share:

• The vision behind the ISF Reference Model
• Key considerations for its adoption across the industry
• What’s next for ISF standardization

See it in action with Agatha

The session also includes a live demonstration of Agatha’s ISF module, showing how to:

• Apply the ISF Reference Model in practice
• Structure and manage your documentation efficiently
• Ensure audit-readiness across your studies

Don’t miss this opportunity to gain practical insights and stay ahead of industry standards.