Informed consent stems from the legal and ethical right an individual has to decide what is done to his or her body, and from the physician's ethical duty to make sure that individuals are involved in decisions about their own health care.
The Nuremberg Code was based on the principle of informed consent rather than beneficence. It established guidelines regarding voluntary participation and the importance of informed and voluntary consent in human experimentation, emphasizing the rights and well-being of individuals involved in research.
Informed consent or free consent is permission granted to another person to perform services such as treatment for medical care. Both verbal and nonverbal communication counts as informed or free consent.
The result of informed consent is greater safety and protection for patients, physicians, and society.
Informed non-consent is the refusing of a procedure while being fully informed of the risks to health and the possible outcome of the patients decision.
it is called informed consent
informed consent form
James E. Ludlam has written: 'Informed consent' -- subject(s): Informed consent (Medical law)
Investigators must obtain informed consent if the study involves interactions with research participants.Investigators must obtain informed consent if the study involves interventions with research participants.Investigators must obtain informed consent if the study involves collection of private information from or about research participants.All of the aboveD: All of the above
should informed consent be a process rather than a one time event
[if the questioner is actually asking about "Informed CONSENT - see discussion page]
You know ramifications of your decision
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