Clinical Trials: Good Clinical Practice
About this course
The series walks you through the International Council for Harmonisation’s Good Clinical Practice guidelines, covering how to protect trial participants, keep data trustworthy, and stay compliant with global regulations. It breaks down the core principles, documentation standards, and ethical considerations that underpin reliable clinical research. Material is presented as a sequence of modules that mix short video lectures with case examples and self‑check quizzes, letting you apply the concepts to real‑world scenarios.
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What you'll learn
- Explain the key components of ICH Good Clinical Practice
- Identify procedures for ensuring participant safety in trials
- Apply data management standards to maintain trial integrity
- Demonstrate compliance with international regulatory requirements
Course objectives
- Provide a foundational understanding of GCP for investigators and clinical researchers
- Equip learners with practical knowledge to conduct ethical and compliant clinical studies
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