Lecture
This lecture covers the general framework of regulations for biomedical research involving human beings and the reuse of their biological material, discussing why and how this field is regulated, the types of research projects involved, the authorization process, the ethical considerations, and the legal aspects in Switzerland and other countries. It also explores the different categories of research risks, the principles of consent, the role of ethics committees, and the evaluation of research protocols, emphasizing the protection of human dignity and health. The lecture delves into the complexities of research involving vulnerable populations, the authorization process, and the challenges related to obtaining consent and conducting research ethically.