Abstract
Introduction 1. Informed consent in medical research - a procedure stretched beyond breaking point? 2. Beyond consent: the trust-based obligations of physicians to patients in clinical research 3. Consent and private liability in clinical research 4. The decision to refuse consent to participation in a clinical trial: does a double standard exist? 5. Beyond a rebarbative commitment to consent 6. The normative status of the requirement to gain an informed consent in clinical trials: comprehension, obligations and empirical evidence 7. Is there an obligation to participate in medical research? 8. Consent with older people: research as a virtuous relationship 9. Towards supported decision-making in biomedical research with cognitively vulnerable adults 10. Is consent sufficient? - a case study of qualitative research with men with intellectual disabilities 11. Consent to genetic testing: a family affair? 12. Cultural authority of informed consent: indigenous participation in biobanking and salmon genomics focus groups Conclusion
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