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This 30 - 40 minute course is an interactive primer to the International Conference on Harmonization’s Good Clinical Practice (ICH/GCP). It introduces you to the key roles and responsibilities of the Sponsor, Investigator and IRB/IEC. In three compact lessons, you will learn the principles around ICH/GCP—before, during and after a clinical trial. Included are reality-based clinical trial scenarios, which provide a solid better foundation to apply ICH/GCP principles.