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O consentimento informado é documentado por meio de um termo de consentimento informado escrito, assinado e datado. [ 23] Na pesquisa médica [en], o Código de Nuremberg estabeleceu um padrão internacional básico em 1947, que continuou a se desenvolver, por exemplo, em resposta à violação ética no Holocausto.
9 de jul. de 2020 · Informed consent is the process in which a health care provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention. The patient must be competent to make a voluntary decision about whether to undergo the procedure or intervention.
- 2023/06/05
Informed consent is a principle in medical ethics, medical law and media studies, that a patient must have sufficient information and understanding before making decisions about their medical care.
2 de mar. de 2017 · Informed consent, which is ethically essential in most clinical research, respects persons’ rights to decide whether participation in the research is compatible with...
Abstract. Informed consent process is the cornerstone of ethics in clinical research. Obtaining informed consent from patients participating in clinical research is an important legal and ethical imperative for clinical trial researchers.
- Rashmi Ashish Kadam
- 10.4103/picr.PICR_147_16
- 2017
- Jul-Sep 2017
11 de out. de 2019 · Informed consent is a process that lets you decide which medical treatments you want or don't want. Learn what it is, when it's needed, what it should include, and why it's important for your health and well-being.
Informed Consent. Download PDF CME Course. Informed consent to medical treatment is fundamental in both ethics and law. Patients have the right to receive information and ask questions about recommended treatments so that they can make well-considered decisions about care.
