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> Search Results: subjectheading:[Human experimentation in medicine -- Law and legislation -- United States.]
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University of Southern Indiana
7
records found
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1.
Regulating human research : IRBs from peer review to compliance bureaucracy / Sarah Babb.
Babb, Sarah L., author.
Stanford, California : Stanford University Press, [2020]
2020
R852.5 .B333 2020
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2.
Experimenting with the consumer [electronic resource] : the mass testing of risky products on the American public / Marshall S. Shapo.
Shapo, Marshall S., 1936-
Westport, Conn. : Praeger, 2009.
KF1296 .S428 2009
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3.
Regulating human research : IRBs from peer review to compliance bureaucracy / Sarah Babb.
Babb, Sarah L., author.
;
ProQuest (Firm)
Stanford, California : Stanford University Press, [2020]
R852.5 .B33 2020
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4.
Proposed revisions to the common rule [electronic resource] : perspectives of social and behavioral scientists / Robert Pool, rapporteur ; Commit[...]
Workshop on Proposed Revisions to the Common Rule in Relation to the Behavioral [...]
Washington, District of Columbia : The National Academies Press, [2013]
©2013
H62 .W67 2013eb
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5.
Clinical research and the law [electronic resource] / Patricia M. Tereskerz ; consulting clinical editors, Robert Edelman, Ross McKinney, Jr.
Tereskerz, Patricia M.
Chichester, West Sussex : John Wiley & Sons, 2012.
QH319.A1 T47 2012eb
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6.
Experimenting with the consumer : the mass testing of risky products on the American public / Marshall S. Shapo.
Shapo, Marshall S., 1936-
Westport, Conn. : Praeger, 2009.
KF1296 .S428 2009
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7.
Clinical trial subjects : adequate FDA protections? : hearing before the Committee on Government Reform and Oversight, House of Representatives, [...]
United States. Congress. House. Committee on Government Reform and Oversight.
Washington : U.S. G.P.O. : For sale by the U.S. G.P.O., Supt. of Docs., Congressional Sales Office, 1998.
KF27 .G6 1998e
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