Explores European regulations for medical devices, covering classification, manufacturer's role, post-market follow-up, and essential requirements compliance.
Explores the legal framework for biomedical research with human beings, covering regulations, authorization, ethical considerations, and challenges in research involving vulnerable populations.
Delves into catastrophes, from the Lisbon earthquake to the Anthropocene, exploring shifts from providentialist to scientific paradigms and the collapse of industrial civilization.
Explores ethical considerations in research participation, including compensation for biological material and the balance between utilitarian and deontological ethics.