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Study guide for institutional review board : management and function
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ISBN: 9780763738662 0763738662 Year: 2006 Publisher: Boston, MA: Jones and Bartlett,

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Institutional review board : member handbook
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ISBN: 0763741221 9780763741228 Year: 2007 Publisher: Sudbury, Mass.: Jones and Bartlett,

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Guidance for institutional review boards (IRBs) : frequently asked questions, IRB registration.
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Year: 2009 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner,

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Guidance for industry : IRB review of stand-alone HIPAA authorizations under FDA regulations.
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Year: 2003 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner,

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Ethical imperialism : institutional review boards and the social sciences, 1965-2009
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ISBN: 0801894905 9780801894909 Year: 2010 Publisher: Baltimore (Md.): Johns Hopkins University press,

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Working effectively with and within IRBs : a practical guide for investigators, sponsors and IRB members.
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ISBN: 1555720838 Year: 2005 Publisher: Hagerstown University publishing group

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Clinical research professionals need a direct, practical guide to working together to protect human research subjects. This book is a reference for research sponsors, investigators, and IRB members, with documents created by the Biomedical Research Alliance of New York: - Sample More...pediatric subject assent form - Sample HIPAA authorization form - Sample assent form for genetic testing and/or tissue banking - Sample evaluation/feedback tool for educational programs - Glossary of lay terms for preparing informed-consent documents. - Nuremberg Code, Declaration of Helsinki, Belmont Report, the Common Rule are included.


Book
Guidance for institutional review boards (IRBs) : frequently asked questions, IRB registration.
Author:
Year: 2009 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner,

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Book
Guidance for industry : IRB review of stand-alone HIPAA authorizations under FDA regulations.
Author:
Year: 2003 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Office of the Commissioner,

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Final report on low-volume institutional review boards.
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Year: 1998 Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General,

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Information sheet : guidance for institutional review boards and clinical investigators (cooperative research)
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Year: 1998 Publisher: [Rockville, MD] : [U.S. Dept. of Health and Human Services, Food and Drug Administration],

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