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Subjects (1-8 of 8)
Human experimentation in medicine -- Law and legislation -- United States
1
1998
Clinical trial subjects : adequate FDA protections? : hearing before the Committee on Government Reform and Oversight, House of Representatives, One Hundred Fifth Congress, second session, April 22, 1
United States. Congress. House. Committee on Government Reform and Oversight.
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Electronic Resources
2
2002
Compact Regs Parts 50, 54, 56, And 312 : CFR 21 Parts 50, 56, and 312 Good Clinical Practices (10 Pack)
United States. Food and Drug Administration.
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Electronic Resources
3
2003
Compact regs parts 50, 54, 56 and 312 : Code of federal regulations 21, parts 50, 54, 56 and 312, good clinical practices
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Electronic Resources
4
2009
Experimenting with the consumer : the mass testing of risky products on the American public
Shapo, Marshall S., 1936-
Westport, Conn. : Praeger, 2009
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KN 39.P6 Sha/Ewt
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5
2009
Experimenting with the consumer : the mass testing of risky products on the American public
Shapo, Marshall S., 1936-
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Electronic Resources
6
2013
Proposed revisions to the common rule : perspectives of social and behavioral scientists
Workshop on Proposed Revisions to the Common Rule in Relation to the Behavioral and Social Sciences (2013 : Washington, D.C.), issuing body.
Washington, District of Columbia : The National Academies Press, [2013]
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7
2020
Regulating human research : IRBs from peer review to compliance bureaucracy
Babb, Sarah L., author
Stanford, California : Stanford University Press, [2020]
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8
2020
What it means to be human : the case for the body in public bioethics
Snead, O. Carter, author.
Cambridge, Massachusetts ; London, England : Harvard University Press, 2020
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