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Library Catalog
Summary
The National Institutes of Health (NIH) invests over {dollar}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.
Call Number
R 852.5 .A46 2021
Edition
3rd ed.
Publication
Burlington, Massachusetts : Jones & Bartlett Learning, 2021
Description
pages cm.
Subjects
Ethics Committees, Research - Organization & Administration
Contents and Notes
Ethical and Historical Background -- Organizing the IRB Office -- Organizing the IRB Committee -- SingleCentral 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.
Authors and Contributors
Bankert, Elizabeth A Gordon, Bruce G Hurley, Elisa A Shriver, Sharon P Public Responsibility in Medicine and Research Association
System ID
785c938ab1
ISBN
9781284181159
Authors and Contributors
Bankert, Elizabeth A
Gordon, Bruce G
Hurley, Elisa A
Public Responsibility in Medicine and Research Association
Shriver, Sharon P
Forms and Genres
Book
Non-Fiction
Subjects
Ethics Committees, Research
Organization & Administration
