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  1. Fostering IRB Collaboration for Review of International Research.Francis Barchi, Megan Kasimatis Singleton & Jon F. Merz - 2014 - American Journal of Bioethics 14 (5):3-8.
    This article presents a review of the literature, summarizes current initiatives, and provides a heuristic for assessing the effectiveness of a range of institutional review board collaborative strategies that can reduce the regulatory burden of ethics review while ensuring protection of human subjects, with a particular focus on international research. Broad adoption of IRB collaborative strategies will reduce regulatory burdens posed by overlapping oversight mechanisms and has the potential to enhance human subjects protections.
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  • Moral conflict in clinical trials.Maria Merritt - 2005 - Ethics 115 (2):306-330.
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  • Seven vulnerabilities in the pediatric research subject.Kenneth Kipnis - 2003 - Theoretical Medicine and Bioethics 24 (2):107-120.
    Most recent thinking about thevulnerability of research subjects uses a``subpopulation'' focus. So conceived, theproblem is to work out special standards forprisoners, pregnant women, the mentally ill,children, and similar groups. In contrast, an``analytical'' approach would identifycharacteristics that are criteria forvulnerability. Using these criteria, one couldsupport a judgment that certain individuals arevulnerable and identify needed accommodationsif they are to serve as research subjects.Seven such characteristics can be evident inchildren: they commonly lack the capacity tomake mature decisions; they are subject to theauthority of (...)
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