This compact two-day Good Clinical Practice course is designed in accordance with the requirements of Swissethics and covers the Good Clinical Practice knowledge essential for investigators of clinical trials and their teams. The course consists of a comprehensive overview of ICH-GCP with a focus on the GCP principles, participant protection, informed consent and safety reporting, as well as topics such as study design, data management and submission to ethics committees in Switzerland. The course is ideal for investigators, study personnel and people involved in and/or interested in clinical research. The course is suitable for beginners as well as experienced investigators who need a refresher or need to acquire a certificate.

The course has been accredited by Swissethics since 2016 and listed with TransCelerate since 2017.

Participants benefit from the extensive experience of our teachers. All teachers have many years of hands-on clinical operations, both in Switzerland and in resource-limited countries.

The course is designed for medical, nursing and scientific staff involved in clinical trials, students as well as individuals who support clinical research activities, such as laboratory personnel, IT and finance professionals.