Course Content This compact two-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.
Target Audience The course is ideal for Investigators, study personnel and people involved and/or interested in clinical research and suited to beginners as well as experienced investigators in need of refresher training.
Certifications The course is accredited by Swissethics and TransCelerate listed. It fulfills the training requirements for investigators and sub-investigators. To receive a certificate of training, participants will need to pass a competency assessment.
