informed consent → συναίνεση μετά από ενημέρωση, συγκατάθεση μετά από ενημέρωση, εν επιγνώσει συναίνεση
Informed consent is a process for getting permission before conducting a healthcare intervention on a person, for conducting some form of research on a person, or for disclosing a person's information. A health care provider may ask a patient to consent to receive therapy before providing it, a clinical researcher may ask a research participant before enrolling that person into a clinical trial, and a researcher may ask a research participant before starting some form of controlled experiment. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics.
Informed consent - Wikipediaar: موافقة مستنيرة; ca: consentiment informat; cs: informovaný souhlas; da: informeret samtykke; de: informierte Einwilligung; en: informed consent; es: consentimiento informado; et: teadlik nõusolek; fi: tietoon perustuva suostumus; fr: consentement libre et éclairé; he: הסכמה מדעת; hr: informirani pristanak; it: consenso informato; ja: インフォームド・コンセント; ko: 사전동의; nl: geïnformeerde toestemming; no: informert samtykke; pl: świadoma zgoda na udział w badaniu; pt: consentimento informado; ru: информированное добровольное согласие; simple: informed consent; uk: інформована згода пацієнта; zh: 知情同意