Red Nucleus Training Institute

Providing on-demand training solutions

Global Regulatory Landscape: Key Differences

~0.50 hrs | GCP - Regulations, Guidance, & Submissions

This module provides an overview of the regulatory differences and requirements for conducting clinical trials for medicinal products in human participants in the United States, Europe, Canada, China, and Japan.

Module Details

After completing this module, you will be able to:
• Compare the key global regulatory differences for clinical trials
• Identify different roles and responsibilities within the global regulatory landscape

Features

• 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?