IRB Information Sheet
Author | : United States. Food and Drug Administration |
Publisher | : |
Total Pages | : 84 |
Release | : 1984 |
Genre | : |
ISBN | : |
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Author | : United States. Food and Drug Administration |
Publisher | : |
Total Pages | : 84 |
Release | : 1984 |
Genre | : |
ISBN | : |
Author | : United States. Food and Drug Administration |
Publisher | : |
Total Pages | : 0 |
Release | : 1984 |
Genre | : |
ISBN | : |
Author | : Robert J. Amdur |
Publisher | : Jones & Bartlett Publishers |
Total Pages | : 224 |
Release | : 2010-10-22 |
Genre | : Medical |
ISBN | : 1449609929 |
The Essential Resource for All IRB Members! Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. NEW CHAPTERS in this Edition Include: * Definition of Human Subject Research, Exempt & Expedited Review Categories * IRB Member Conflict of Interest All chapters are completely updated for 2010 practice! This handbook is an excellent accompaniment to Institutional Review Board: Management and Function, Second Edition and the Study Guide that IRB members can access and refer to quickly and easily.
Author | : United States. National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research |
Publisher | : |
Total Pages | : 614 |
Release | : 1978 |
Genre | : Ethics, Medical |
ISBN | : |
Author | : Laura Stark |
Publisher | : University of Chicago Press |
Total Pages | : 242 |
Release | : 2012-02 |
Genre | : History |
ISBN | : 0226770869 |
Drwaing on extensive archival sources, Laura Stark reconstructs the daily lives of scientists, lawyers, administrators, and research subjects working - and 'warring' - on the campus of the National Institutes of Health, where they first wrote the rules for the treatment of human subjects.
Author | : Robert J. Amdur |
Publisher | : Jones & Bartlett Learning |
Total Pages | : 130 |
Release | : 2021-01-15 |
Genre | : Medical |
ISBN | : 1284233634 |
Designed to give Institutional Review Board (IRB) members the information they need to protect the rights and welfare of research subjects in a way that is both effective and efficient, the chapters of the Institutional Review Board Member Handbook are short and to the point. Topic-specific chapters list the criteria IRB members should use to determine how to vote on specific kinds of studies and offer practical advice on what IRB members should do before and during full-committee meetings. This handbook is an excellent accompaniment to Institutional Review Board: Management and Function, Third Edition (ISBN: 978-1-284-18115-9) and the Study Guide that IRB members can access and refer to quickly and easily. The book has three sections: -Part 1: Background Information, containing background information on human subject research -Part 2: The Full Committee IRB Meeting, comprised of eight chapters focused on the research proposal review process.
Author | : Robert Klitzman |
Publisher | : Oxford University Press, USA |
Total Pages | : 433 |
Release | : 2015 |
Genre | : Medical |
ISBN | : 0199364605 |
Studies on humans have saved countless lives, but sometimes harm participants. Research ethics committees currently monitor scientists, but have been increasingly criticized for blocking important research. How these committees work, however, is largely unknown. This book uniquely illuminates this hidden world that ultimately affects us all.
Author | : Elizabeth A. Bankert |
Publisher | : Jones & Bartlett Learning |
Total Pages | : 568 |
Release | : 2006 |
Genre | : Institutional review boards (Medicine) |
ISBN | : 9780763730499 |
This comprehensive reference covers three separate areas related to IRBs: administration, daily management; and ethical issues. This instructional manual provides IRB members and administrators with the information they need to run an efficient and effective system of protecting human research subjects, while remaining in compliance with federal research regulations. The text includes case studies, sample forms, and sample policy documents. The updated Second Edition includes seven new chapters: IRB Closure of Study Files, Internet Research, Research in Public Schools, Phase I Clinical Trials in Healthy Volunteers, Vulnerability in Research, Balancing the Risks and Potential Benefits,and HIPAA.