Informed consent is one of the most crucial processes in the clinical trials. It is also one of the most complicated processes if we consider all special cases like consenting of minors or incapacitated subjects or emergency trials. Inspections and audits findings show that there is a need of constant re-training of investigators but also study teams including CRAs. CRAs play important role ensuring the consent process is properly performed and documented. This course provides information on consenting of subjects who cannot give the consent independently. The main part is dedicated to verification of consent process and issues reporting. There are also sections covering Informed Consent From adaptation to local requirements and translation. During the course, participant will be provided with real examples of informed consent forms and source documents to better understand how to work with this document and how to verify the consent process. Course is followed by bank of questions and case study exercise so the participant can verify the knowledge.