This compact one and a half-day Good Clinical Practice course is designed in accordance with the requirements of Swissethics and covers the Good Clinical Practice knowledge indispensable for Investigators of clinical trials. The course consists of a comprehensive overview of ICH-GCP with a focus on participant protection, informed consent and safety reporting as well as topics such as study design and data management. It is ideal for Investigators, study personnel and people involved and/or interested in clinical research. The course is suited to beginners as well as experienced investigators in need of refresher training.