Medical risk and the right to an informed consent in clinical care and clinical research |
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Contents
TABI E OF CONTENTS | |
Medical Risk and Informed Consent in Clinical | |
The Reasonable Person Standard 1972Present 41 | |
Copyright | |
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adverse outcome alternatives asked Beecher cancer Canterbury court chance cian clinical research study cognitive committee communication competent concept conflict of interest consent in clinical court argued court decision Declaration of Helsinki disclosed discuss drug and product drug or product ethical experience Faden and Beauchamp Federal Regulations focused hospital Ibid information disclosure information patients informed consent informed consent form institutional review board Involving Human Subjects judicial Lord Diplock Lord Scarman low probability medical decision medical intervention medical risk numbers Nuremberg Code occur operation opinion participation patient decision patient informedness patient preferences patient-physician decision patient-physician relationship patients and physicians patients understand percent perspective physi placebo potential principal investigator problems procedure professional standard prostate prostate cancer questions rational reasonable person standard regarding Research Involving Human responsible risk disclosure scientific South Western Reporter Stevens Johnson Syndrome surgeon surgery survival tardive dyskinesia Texas Supreme Court therapeutic therapy tion treatment Vanderpool Veatch versus