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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 rebar... MORE | 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 |
| Table of Contents provided by Ingram. All Rights Reserved. |