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  1.  29
    Consent forms and the therapeutic misconception.Nancy M. P. King, Gail E. Henderson, Larry R. Churchill, Arlene M. Davis, Sara Chandros Hull, Daniel K. Nelson, P. Christy Parham-Vetter, Barbra Bluestone Rothschild, Michele M. Easter & Benjamin S. Wilfond - 2005 - IRB: Ethics & Human Research 27 (1):1-7.
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  2.  28
    Assessing Benefits in Clinical Research: Why Diversity in Benefit Assessment Can Be Risky.Larry R. Churchill, Daniel K. Nelson, Gail E. Henderson, Nancy M. P. King, Arlene M. Davis, Erin Leahey & Benjamin S. Wilfond - 2003 - IRB: Ethics & Human Research 25 (3):1.
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  3.  24
    The Irregular Terrain of Human Subjects Research Regulations.David Forster, Daniel K. Nelson, David Borasky & Jeffrey R. Botkin - 2014 - Hastings Center Report 44 (s3):29-30.
    The overlap and differences between the parallel regulatory systems for research create ample room for confusion and missteps, as discussed by Barbara Bierer and Mark Barnes in their report in this supplement. In practice, beyond the inherent differences in the two systems of regulations themselves, there are many issues that further complicate the application of these regulations. These include the variation in size of the institutions receiving PHS funding, the increased prevalence of multisite research, the allocation of research conduct and (...)
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  4.  31
    Dollars and Deadlines: Rule Reforms in Short Time Frames.Toby Schonfeld, Melinda Gormley & Daniel K. Nelson - 2017 - American Journal of Bioethics 17 (7):62-64.
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  5.  21
    Reflections From Fellow Feds: Addressing Delays in Oversight of Federally Funded Research.Toby Schonfeld & Daniel K. Nelson - 2016 - American Journal of Bioethics 16 (8):50-52.
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