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Medical/Healthcare law and ethics
Medical/Healthcare law and ethics

... – increased frequency & difficulty due to: • increased technology – life-saving/life-sustaining procedures/treatments • changing doctor-patient relationship – beneficence+paternalism → autonomy+justice+rights • changing doctor-healthcare professional relationship – professional roles; specialisation ...
research_ethics_2011 - ethicsandcriticalreasoning
research_ethics_2011 - ethicsandcriticalreasoning

... Why did the injections continue after adverse effects became evident? ...
What is medical ethics? A-Ethics (Gr) ethikos , adjuctive, noun, ethos
What is medical ethics? A-Ethics (Gr) ethikos , adjuctive, noun, ethos

... a- It is the patient who is being treated not simply the disease “First we must consider the nature of man in general and each of individual and the charecteristics of each disease” (Hippocrates epidemic) ...
MCRTP Responsible Conduct of Research
MCRTP Responsible Conduct of Research

... Constitutional dimension – substantive due process (privacy as “the right to be let alone”) Underlying moral principle more aptly captured by term “authenticity” when patient lacks decisional capacity Balanced in so-called “right to die” litigation by “countervailing interests of the state” ...
論文寫作的心理社會與倫理議題
論文寫作的心理社會與倫理議題

...  Patient’s control over touching, manipulation, ...
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Informed consent

Informed consent is a process for getting permission before conducting a healthcare intervention on a person. A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial. Informed consent is collected according to guidelines from the fields of medical ethics and research ethics.An informed consent can be said to have been given based upon a clear appreciation and understanding of the facts, implications, and consequences of an action. To give informed consent, the individual concerned must have adequate reasoning faculties and be in possession of all relevant facts. Impairments to reasoning and judgment that may prevent informed consent include basic intellectual or emotional immaturity, high levels of stress such as PTSD or a severe intellectual disability, severe mental illness, intoxication, severe sleep deprivation, Alzheimer's disease, or being in a coma.Some acts can take place because of a lack of informed consent. In cases where an individual is considered unable to give informed consent, another person is generally authorized to give consent on his behalf, e.g., parents or legal guardians of a child (though in this circumstance the child may be required to provide informed assent) and conservators for the mentally ill.In cases where an individual is provided insufficient information to form a reasoned decision, serious ethical issues arise. Such cases in a clinical trial in medical research are anticipated and prevented by an ethics committee or Institutional Review Board.Informed Consent Form Templates can be found on the World Health Organization Website for practical use.
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