Analysis of the Nature of IRB Contingencies Required for Informed Consent Document Approval-Reference-Cited by-同舟云学术

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Analysis of the Nature of IRB Contingencies Required for Informed Consent Document Approval

Published:2015-04-21 Issue:4 Volume:22 Page:237-245
ISSN:0898-9621
Container-title:Accountability in Research
language:en
Short-container-title:Accountability in Research

Author:

Blackwood R. Alexander,Maio Ronald F.,Mrdjenovich Adam J.,VandenBosch Terry M.,Gordon Patricia S.,Shipman Emily L.,Hamilton Ted A.

Publisher

Informa UK Limited

Subject

Library and Information Sciences,Education,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.1080/08989621.2014.956866

Reference12 articles.

1. A Systematic Review of the Empirical Literature Evaluating IRBs: What We Know and What We Still Need to Learn

2. Online Survey Tools: Ethical and Methodological Concerns of Human Research Ethics Committees

3. Working with the institutional review board

4. How Many Protocols Are Deferred? One IRB's Experience

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2. Ethical Considerations in Clinical Trials for Disorders of Consciousness;Brain Sciences;2022-02-02

3. Measuring IRB Regulatory Compliance: Development, Testing, and Use of the National Cancer Institute StART Tool;Journal of Empirical Research on Human Research Ethics;2019-03-13

4. Research Ethics Committees’ Oversight of Biomedical Research in South Africa: A Thematic Analysis of Ethical Issues Raised During Ethics Review of Non-Expedited Protocols;Journal of Empirical Research on Human Research Ethics;2019-01-24

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