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Is the doctrine of informed consent law?
Informed consent is an ethical principle in healthcare that requires healthcare providers to disclose information to patients so they can make voluntary and informed decisions about their care. While not technically a law in the sense of being a statute, informed consent is supported by legal precedents and regulations in many jurisdictions to protect patients' rights and autonomy.
What is the doctrine of informed choice?
[if the questioner is actually asking about "Informed CONSENT - see discussion page]
What protects patients from being coerced into treatment?
Doctrine of informed consent
What are three exceptions to the informed consent doctrine?
Study smartly and healthy
What counts as informed consent or free consent?
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.
What is the outcome of using informed consent?
The result of informed consent is greater safety and protection for patients, physicians, and society.
What is informed non-consent?
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.
What is focus interview?
informed consent form
What has the author James E Ludlam written?
James E. Ludlam has written: 'Informed consent' -- subject(s): Informed consent (Medical law)
When might human subject research require investigators to obtain informed consent?
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
What are the basic elements of informed consent?
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.
Informed consent should be a process rather than a one-time event?
should informed consent be a process rather than a one time event
