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  1. The historical foundations of the research-practice distinction in bioethics.Tom L. Beauchamp & Yashar Saghai - 2012 - Heoretical Medicine and Bioethics 33 (1):45-56.
    The distinction between clinical research and clinical practice directs how we partition medicine and biomedical science. Reasons for a sharp distinction date historically to the work of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research, especially to its analysis of the “boundaries” between research and practice in the Belmont Report (1978). Belmont presents a segregation model of the research-practice distinction, according to which research and practice form conceptually exclusive sets of activities and interventions. This (...)
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  • (1 other version)Reform within the common rule?Tom Puglisi - 2013 - In Mildred Z. Solomon & Ann Bonham (eds.), Ethical oversight of learning health care systems. [Malden, Mass.]: Wiley-Blackwell. pp. 40-42.
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  • (1 other version)Reform within the Common Rule?Tom Puglisi - 2013 - Hastings Center Report 43 (s1):40-42.
    In their papers in this supplement, Ruth Faden and colleagues conclude that research ethics and regulation must change to accommodate a changed and changing health care environment. The reality, however, is that the widely understood and accepted ethical framework embedded in the regulatory requirements known as the Common Rule, and recent proposals to modify the Common Rule have become stalled, at least for the foreseeable future, if not permanently. Meaningful systemic modernization of the Common Rule is not likely to occur (...)
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  • Comment on the Proposed Regulations from Higher Education and Professional Social Science Associations.J. W. Peltason - 1980 - IRB: Ethics & Human Research 2 (2):10.
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  • An Assessment of the Human Subjects Protection Review Process for Exempt Research.Jonathan D. Loe, D. Alex Winkelman & Christopher T. Robertson - 2016 - Journal of Law, Medicine and Ethics 44 (3):481-491.
    Medical and public health research includes surveys, interviews, and biospecimens — techniques that do not present substantial risks to subjects. Consequently, this research is exempt from regulation under the Federal Common Rule. Nevertheless, at many institutions, exempt research is frequently subject to the same regulatory process that is required for non-exempt research, requiring the consumption of time and resources for review by Institutional Review Board members or staff. The federal government has indicated an intention to reform and centralize this system, (...)
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  • Ethical Imperialism: Institutional Review Boards and the Social Sciences, 1965–2009.[author unknown] - 2010
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