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Informed Consent In Surgery

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... approve the IND, and annual progress reports must be sent to the FDA. The next phase is clinical trials. Volunteers in all three phases of the clinical trials must give informed consent * Reproductive issues, rights and informed consent. * Ways in which genetic information could affect the minorities. greater good. In these cases, cost versus benefits must be weighed, all actions must be humane, and informed consent of these experiments--which have the potential to harm people--to ethically continue, informed consent from the test such access legal. Informed consent is associated with extension of a written account of why personal information is ...



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Sources list for INFORMED CONSENT IN SURGERY:

Ogloff, J. R. (1991). Are research participants truly informed? Readability of informed consent forms used in research. Ethics & Behavior, 1(4), 239-252.
Ethical Failures

Wear, S. (1998). Informed consent: Patient autonomy and clinician beneficence within health care. Washington, DC: Georgetown University Press.
Informed Consent and the Vulnerable Therapist

Fisher, C. B. (2002). A goodness-of-fit ethic for informed consent. Fordham Urban Law, 30(1), 159.
Informed Consent and the Vulnerable Therapist

Sulmasy, D. P. (2002). Informed consent without autonomy. Fordham Urban Law Journal, 30(1), 207.
Informed Consent and the Vulnerable Therapist

Karlawish JHT; Fox E; Pearlman R; How Changes in Health Care Practices, Systems, and Research Challenge the Practice of Informed Consent.. Medical Care 2002; 40(9 Suppl): V 12-20.
Thrombolysis for Myocardial Infarction in Accident and Emergency

 

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