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.
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
There are many basic elements of informed consent. Some of them are discomforts to the subject, study that involve research, a statement with participatory voluntary.
[if the questioner is actually asking about "Informed CONSENT - see discussion page]
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You know ramifications of your decision
state law
The Mississippi - 1982 Informed Consent 2-15 was released on: USA: 24 January 1984