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  1. Responding to the challenge of the children's health act: An introduction to children in research.Lainie Friedman Ross - 2003 - Theoretical Medicine and Bioethics 24 (2):101-106.
    This overview describes the breadth of topicscovered in this volume devoted to children inresearch. It summarizes how these articles areinterrelated and how they all respond to thechallenge proposed by the Children's Health Actof 2000: to consider what modifications, ifany, are necessary to current regulations ``toensure the adequate and appropriate protectionof children participating in research.''.
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  • Autonomie, don et partage dans la problématique de l'expérimentation humaine.Anne Fagot-Largeault - 1991 - Dialogue 30 (3):355-.
    Après avoir, en préambule, défini l'expérimentation humaine au sens qui est ici visé, j'identifierai le don qu'elle implique au sein d'une chaîne de solidarité, puis j'analyserai quelques difficultés auxquelles donne lieu l'intégration culturelle de cette démarche de partage, enfin je mettrai en évidence un conflit entre solidarité et autonomie.
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  • Justice, Fairness, and Membership in a Class: Conceptual Confusions and Moral Puzzles in the Regulation of Human Subjects Research.Ana S. Iltis - 2011 - Journal of Law, Medicine and Ethics 39 (3):488-501.
    Much of the human research conducted in the United States or by U.S. researchers is regulated by the Common Rule. The Common Rule reflects the decision of 17 federal agencies, including the Department of Health and Human Services, to require that investigators follow the same rules for conducting human research., though there is significant overlap with the Common Rule.) Many of the obligations delineated in the Common Rule can be traced back to the work of the National Commission for the (...)
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  • Should we presume moral turpitude in our children? – Small children and consent to medical research.John Harris & Søren Holm - 2003 - Theoretical Medicine and Bioethics 24 (2):121-129.
    When children are too young to make their ownautonomous decisions, decisions have to be madefor them. In certain contexts we allow parentsand others to make these decisions, and do notinterfere unless the decision clearly violatesthe best interest of the child. In othercontexts we put a priori limits on whatkind of decisions parents can make, and/or whatkinds of considerations they have to take intoaccount. Consent to medical research currentlyfalls into the second group mentioned here. Wewant to consider and ultimately reject one (...)
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  • In Defense of the Hopkins Lead Abatement Studies.Lainie Friedman Ross - 2002 - Journal of Law, Medicine and Ethics 30 (1):50-57.
    In August 2001, the Maryland Court of Appeals harshly criticized the Kennedy Krieger Institute of Johns Hopkins University for knowingly exposing poor children to lead-based paint. The court’s decision made national news, and is worth examining because it raises several very important issues for research ethics.The research conducted by the Institute was an attempt to understand how successful different lead abatement programs were in reducing continued lead exposure to children. Previously, Julian Chisolm and Mark Farfel, of John Hopkins University, had (...)
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