Clinical Research - ICH GCP E6(R3)

This foundational course provides a comprehensive overview of the International Council for Harmonization Good Clinical Practice (ICH GCP E6 R3) guidelines, which form the global ethical and scientific standard for designing, conducting, recording, and reporting clinical trials involving human subjects. Participants will gain an in-depth understanding of the core principles, including the protection of human rights, the assurance of safety and well-being for trial participants, and the integrity of clinical trial data. Through practical scenarios, you will learn to apply these critical regulations to ensure compliance, maintain rigorous ethical standards, and contribute to the generation of reliable and defensible clinical research outcomes.