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Research on human subjects : ethics, law, and social policy / edited by David N. Weisstub.

Contributor(s): Material type: TextTextPublication details: Kidlington, Oxford, UK : Pergamon, 1998.Edition: 1st edDescription: xxvi, 658 p. ; 25 cmISBN:
  • 0080434347 (hc.)
  • 9780080434346:
Subject(s): DDC classification:
  • 174.28
Contents:
Ch. 1. The ethical parameters of experimentation-- Ch. 2. Bringing ethics to human experimentation: the American experience-- Ch. 3. Beyond consent-- Ch. 4. Roles in clinical and research ethics-- Ch. 5. The concept of goodness in medical research: an action-theoretic approach-- Ch. 6. Drawing the distinction between therapeutic research and non-therapeutic experimentation: clearing a way through the definitional thicket
Ch. 7. The distinction between "clinical practice" and "research": the case of pituitary derived hormones and Creutzfeldt-Jakob disease-- Ch. 8. "Consensual" research with cognitively impaired adults: resolving legal shortcomings in adult guardianship-- Ch. 9. French law and biomedical research: a practical experiment-- Ch. 10. Consent to human experimentation in Quebec: the application of the civil law principle of personal inviolability to protect special populations
Ch. 11. The advance directive in research: prospects and pitfalls -- Ch. 12. The regulation of human experimentation: historical and contemporary perspectives-- Ch. 13. International trends in research regulation: science as negotiation-- Ch. 14. Models for regulating research: the council of Europe and international trends-- Ch. 15. Research ethics committees and the principle of justice: putting ethics and law to the test
Ch. 16. The institutional review board: Its origins, purpose, function, and future-- Ch. 17. The regulation of biomedical experimentation in Canada: developing an effective apparatus for the implementation of ethical principles in a scientific milieu-- Ch. 18. Establishing the boundaries of ethically permissible research with vulnerable populations-- Ch. 19. Biomedical experimentation with children: balancing the need for protective measures with the need to respect children's developing ability to make significant life decisions for themselves
Ch. 20. Biomedical experimentation involving elderly subjects: the need to balance limited, benevolent protection with recognition of a long history of autonomous decision-making-- Ch. 21. Ethical research with vulnerable populations: the mentally disordered-- Ch. 22. Ethics in psychiatric research with incompetent patients-- Ch. 23. The conditions of personhood as applied to incompetent persons-- Ch. 24. Ethical research with vulnerable populations: the developmentally disabled
Ch. 25. Ethics in research with detained individuals-- Ch. 26. Prisoners as subjects of biomedical experimentation: examining the arguments for and against a total ban-- Ch. 27. Ethical questions pertaining to the use of placebos-- Ch. 28. Resolving the inherent dissonance between the doctor's roles as healer and researcher: a proposal-- Ch. 29. Ethical issues in epidemiological research-- Ch. 30. Ethical guidelines for epidemiological research-- Ch. 31. Epidemiology and the ownership of health data: ethical, legal and social aspects.

Includes bibliographical references (p. 609-658).

Ch. 1. The ethical parameters of experimentation-- Ch. 2. Bringing ethics to human experimentation: the American experience-- Ch. 3. Beyond consent-- Ch. 4. Roles in clinical and research ethics-- Ch. 5. The concept of goodness in medical research: an action-theoretic approach-- Ch. 6. Drawing the distinction between therapeutic research and non-therapeutic experimentation: clearing a way through the definitional thicket

Ch. 7. The distinction between "clinical practice" and "research": the case of pituitary derived hormones and Creutzfeldt-Jakob disease-- Ch. 8. "Consensual" research with cognitively impaired adults: resolving legal shortcomings in adult guardianship-- Ch. 9. French law and biomedical research: a practical experiment-- Ch. 10. Consent to human experimentation in Quebec: the application of the civil law principle of personal inviolability to protect special populations

Ch. 11. The advance directive in research: prospects and pitfalls -- Ch. 12. The regulation of human experimentation: historical and contemporary perspectives-- Ch. 13. International trends in research regulation: science as negotiation-- Ch. 14. Models for regulating research: the council of Europe and international trends-- Ch. 15. Research ethics committees and the principle of justice: putting ethics and law to the test

Ch. 16. The institutional review board: Its origins, purpose, function, and future-- Ch. 17. The regulation of biomedical experimentation in Canada: developing an effective apparatus for the implementation of ethical principles in a scientific milieu-- Ch. 18. Establishing the boundaries of ethically permissible research with vulnerable populations-- Ch. 19. Biomedical experimentation with children: balancing the need for protective measures with the need to respect children's developing ability to make significant life decisions for themselves

Ch. 20. Biomedical experimentation involving elderly subjects: the need to balance limited, benevolent protection with recognition of a long history of autonomous decision-making-- Ch. 21. Ethical research with vulnerable populations: the mentally disordered-- Ch. 22. Ethics in psychiatric research with incompetent patients-- Ch. 23. The conditions of personhood as applied to incompetent persons-- Ch. 24. Ethical research with vulnerable populations: the developmentally disabled

Ch. 25. Ethics in research with detained individuals-- Ch. 26. Prisoners as subjects of biomedical experimentation: examining the arguments for and against a total ban-- Ch. 27. Ethical questions pertaining to the use of placebos-- Ch. 28. Resolving the inherent dissonance between the doctor's roles as healer and researcher: a proposal-- Ch. 29. Ethical issues in epidemiological research-- Ch. 30. Ethical guidelines for epidemiological research-- Ch. 31. Epidemiology and the ownership of health data: ethical, legal and social aspects.

25.01

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