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Contributors | p. xi |
Introduction | p. 1 |
Informed consent in medical research - a procedure stretched beyond breaking point? | p. 11 |
Trust and exploitation in clinical research | p. 25 |
Consent and private liability in clinical research | p. 39 |
The decision to decline to enrol in a clinical trial: a blind spot in the literature on decision-making for research participation | p. 57 |
Beyond a rebarbative commitment to consent | p. 79 |
The normative status of the requirement to gain an informed consent in clinical trials: comprehension, obligations, and empirical evidence | p. 99 |
Is there an obligation to participate in medical research? | p. 115 |
Consenting older adults: research as a virtuous relationship | p. 133 |
Towards supported decision-making in biomedical research with cognitively vulnerable adults | p. 151 |
Is consent sufficient? A case study of qualitative research with men with intellectual disabilities | p. 171 |
Consent to genetic testing: a family affair? | p. 185 |
Cultural authority of informed consent: indigenous participation in biobanking and salmon genomics focus groups | p. 199 |
Consent and beyond: some conclusions | p. 213 |
Index | p. 229 |
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