A Central Institutional Review Board for Multi-Institutional Trials

These are difficult times for the nation's system of protection for human subjects in research. 1 – 10 On the basis of a series of reports, the Office of the Inspector General of the Department of Health and Human Services concluded that institutional review boards (IRBs) are now forced to “rev...

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Veröffentlicht in:The New England journal of medicine 2002-05, Vol.346 (18), p.1405-1408
Hauptverfasser: Killen, Jack, Christian, Michaele C, Abrams, Jeffrey S, McCabe, Mary S, Goldberg, Jacquelyn L, Mauer, Joan K, Wittes, Robert E
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container_end_page 1408
container_issue 18
container_start_page 1405
container_title The New England journal of medicine
container_volume 346
creator Killen, Jack
Christian, Michaele C
Abrams, Jeffrey S
McCabe, Mary S
Goldberg, Jacquelyn L
Mauer, Joan K
Wittes, Robert E
description These are difficult times for the nation's system of protection for human subjects in research. 1 – 10 On the basis of a series of reports, the Office of the Inspector General of the Department of Health and Human Services concluded that institutional review boards (IRBs) are now forced to “review too much, too quickly, with too little expertise,” and with inadequate resources. 6 One consequence is that there is minimal, often perfunctory, review of ongoing research. In addition, IRB members have become disillusioned as a result of both public criticism concerning the perceived failures of the boards and the increasing amount of . . .
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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; New England Journal of Medicine
subjects Bioethics
Biological and medical sciences
Clinical trials
Clinical Trials as Topic
Ethics
Ethics Committees, Research - organization & administration
Humans
Medical research
Medical sciences
Multicenter Studies as Topic
National Institutes of Health (U.S.)
Pilot Projects
Review boards
United States
title A Central Institutional Review Board for Multi-Institutional Trials
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