Abstract
What is the role of the physician? What is the role of the researcher? Are these roles inherently in conflict with each other? If so, are they so much in conflict that when one professional attempts to play both roles simultaneously we should impose special procedural protections for the rights and welfare of the patient—subjects? Or is the conflict so threatening and so incorrigible that we should forbid any professional to play both roles simultaneously?
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References
R. J. Levine, Ethics and Regulation of Clinical Research Baltimore: (Urban & Schwarzenberg, 1981), p. 2.
lbid, pp. 5–6.
Ibid, pp. 55–56.
lbid, p. 92.
H. M. Spiro, “Constraint and consent: On being a patient and a subject,” New England Journal Medicine 293, 1975, 1134–1135.
H. K. Beecher, Research and the Individual: Human Studies Boston: (Little, Brown and Co., 1970), pp. 79–94.
Ibid, pp. 289–290.
Levine, pp. 103–106.
Levine, p. 95ff.
C. Fried, Medical Experimentation: Personal Integrity and Social Policy New York: (American Elsevier Co., 1974), p. 67.
Levine, p. 130.
Levine, p. 104.
Levine, pp. 26–27.
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© 1985 The Humana Press, Inc.
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Levine, R.J. (1985). The Physician—Researcher. In: Melnick, V.L., Dubler, N.N. (eds) Alzheimer’s Dementia. Contemporary Issues in Biomedicine, Ethics, and Society. Humana Press. https://doi.org/10.1007/978-1-4612-5174-3_4
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DOI: https://doi.org/10.1007/978-1-4612-5174-3_4
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