Institutional review board : management and function / [edited by] Elizabeth A. Bankert, Bruce G. Gordon, Elisa A. Hurley, Sharon P. Shriver, Public Responsibility in Medicine & Research (PRIM&R)
"The National Institutes of Health (NIH) invests over $37 billion per year in support of research to improve human health. All research funded by NIH that involves human subjects is subject to regulatory oversight, requiring institutions to staff and manage Institutional Review Boards (IRBs). I...
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| Online Access: |
Full Text (via ProQuest) |
|---|---|
| Other Authors: | , , , |
| Other title: | Institutional review board (Amdur) |
| Format: | eBook |
| Language: | English |
| Published: |
Burlington, Massachusetts :
Jones & Bartlett Learning,
[2021]
|
| Edition: | Third edition. |
MARC
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| 130 | 0 | |a Institutional review board (Amdur) | |
| 245 | 1 | 0 | |a Institutional review board : |b management and function / |c [edited by] Elizabeth A. Bankert, Bruce G. Gordon, Elisa A. Hurley, Sharon P. Shriver, Public Responsibility in Medicine & Research (PRIM&R) |
| 250 | |a Third edition. | ||
| 264 | 1 | |a Burlington, Massachusetts : |b Jones & Bartlett Learning, |c [2021] | |
| 300 | |a 1 online resource. | ||
| 336 | |a text |b txt |2 rdacontent. | ||
| 337 | |a computer |b c |2 rdamedia. | ||
| 338 | |a online resource |b cr |2 rdacarrier. | ||
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 0 | |a Ethical and Historical Background -- Organizing the IRB Office -- Organizing the IRB Committee -- Single/Central IRBs -- Review of Research -- Informed Consent -- IRB Review of Approved Protocols -- Administration, Education, and Regulatory Issues -- Considerations Based on Study Population -- Issues Based on Study Design or Category -- Research Regulated by FDA and Other Agencies -- Special Topics -- Reference Material. | |
| 520 | |a "The National Institutes of Health (NIH) invests over $37 billion per year in support of research to improve human health. All research funded by NIH that involves human subjects is subject to regulatory oversight, requiring institutions to staff and manage Institutional Review Boards (IRBs). IRB members, chairs, and the many associated human subjects protections oversight professionals who support the work of the IRB must navigate complex federal regulations issued by multiple agencies. This book is the industry standard reference work for the research oversight community, providing comprehensive, understandable interpretations of the regulations, clear descriptions of the ethical principles on which the regulations are based, and practical best-practices guidelines for effectively implementing regulatory oversight"-- |c Provided by publisher. | ||
| 700 | 1 | |a Bankert, Elizabeth A., |e editor. | |
| 700 | 1 | |a Gordon, Bruce G., |e editor. | |
| 700 | 1 | |a Hurley, Elisa A., |e editor. | |
| 700 | 1 | |a Shriver, Sharon P., |e editor. | |
| 710 | 2 | |a Public Responsibility in Medicine and Research (Association), |e issuing body. | |
| 776 | 0 | 8 | |i Print version: |z 9781284181159 |w (DLC) 2020044754 |w (OCoLC)1198988816. |
| 856 | 4 | 0 | |u http://ebookcentral.proquest.com/lib/ucb/detail.action?docID=6485074 |z Full Text (via ProQuest) |
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| 948 | |a May 2024 ebook central cleanup, msw. | ||
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