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Bioethics
Volume 19
Part 2
$32.99 (C)
Part of Social Philosophy and Policy
- Editors:
- Ellen Frankel Paul, Bowling Green State University, Ohio
- Fred D. Miller, Jr, Bowling Green State University, Ohio
- Jeffrey Paul, Bowling Green State University, Ohio
- Date Published: July 2002
- availability: Available
- format: Paperback
- isbn: 9780521525268
$
32.99
(C)
Paperback
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Fifteen philosophers, social scientists, and academic lawyers assess various aspects of bioethics. Some detail its development and challenge the field's basic assumptions. Others consider bioethics's role in contemporary society and examine it in policy administration as well as in its interaction with other branches of philosophical inquiry. Chapters also focus on specific issues, including the responsibilities of researchers to subjects in clinical trials; the proper criteria for determining when a living organism has died; the allocation of scarce, life-saving medical resources; and the subsidization of pharmaceutical products for those who may be deprived of the benefits of modern medicine.
Read more- Fifteen philosophers, social scientists, and academic lawyers assess various aspects of this field
- Bioethicists counsel healthcare practitioners, patients, and their families
- Bioethicists analyze and assess moral dilemmas raised by medical research and innovative treatments
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×Product details
- Date Published: July 2002
- format: Paperback
- isbn: 9780521525268
- length: 418 pages
- dimensions: 228 x 153 x 23 mm
- weight: 0.56kg
- availability: Available
Table of Contents
1. Bioethics and the problem of pluralism
2. Pragmatism in bioethics: been there, done that
3. The ordination of bioethicists as secular moral experts
4. Information(al) matters: bioethics and the boundaries of the public and the private
5. Bioethics as social philosophy
6. Social moral epistemology
7. Why health is not special: errors in evolved bioethics intuitions
8. Power, integrity, and trust in the managed practice of medicine: lessons from the history of medical ethics
9. The distribution of life-saving medical resources: equality, life expectancy, and choice behind the veil
10. Pharmacogenetic interventions, orphan drugs, and distributive justice: the role of cost-benefit analysis
11. The ubiquity and utility of the therapeutic misconception
12. Indifference of subjects: an alternative to equipoise in randomized clinical trials
13. The biophilosophical basis of whole-brain death
14. Freedom and responsibility in genetic testing
15. Genes, justice, and obligations to future people.Editors
Ellen Frankel Paul, Bowling Green State University, Ohio
Fred D. Miller, Jr, Bowling Green State University, Ohio
Jeffrey Paul, Bowling Green State University, Ohio
Contributors
Donald C. Ainslie, John D. Arras, H. Tristram Engelhardt, Jr., Lisa S. Parker, Kevin Wm. Wildes, Allen Buchanan, Robin Hanson, Laurence B. McCullough, Mark S. Stein, Arti K. Rai, Rebecca Dresser, Robert M. Veatch, James L. Bernat, Baruch A. Brody, F. M. Kamm
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