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Red Nucleus Training Institute

Providing on-demand training solutions

Clinical Trials: Adverse Events

Clinical Trials: Adverse Events

Clinical Trials: Adverse Events

~0.50 hrs | GCP - Clinical Operations & Process

In this module, you will receive an overview of the types of Adverse Events (AE), how to report them, where to report them, and how to establish an AE reporting system.

Module Details

After completing this module, you will be able to:
• Define and explain adverse events, SUSAR, and SAEs
• Identify the new formats for reporting clinical trial results and adverse events
• Recognize the current timeframes for registering and updating and other global repositories


• Audio narration with on-demand full-text transcript
• Module-level interactive learning exercises and
self-check questions
• Fully cited and sourced from a blend of Red Nucleus
best practices and global health authority regulations
and guidance
• Updated annually
• SCORM compliant

Interested in learning more about this course?

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