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Nicole Deming [4]Nicole M. Deming [1]
  1. Nicole Deming (forthcoming). Rebecca Dresser is Daniel Noyes. Hastings Center Report.
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  2. Aaron J. Goldenberg, Karen J. Maschke, Steven Joffe, Jeffrey R. Botkin, Erin Rothwell, Thomas H. Murray, Rebecca Anderson, Nicole Deming, Beth F. Rosenthal & Suzanne M. Rivera (2015). IRB Practices and Policies Regarding the Secondary Research Use of Biospecimens. BMC Medical Ethics 16 (1):32.
    As sharing and secondary research use of biospecimens increases, IRBs and researchers face the challenge of protecting and respecting donors without comprehensive regulations addressing the human subject protection issues posed by biobanking. Variation in IRB biobanking policies about these issues has not been well documented.
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  3. M. Aulisio, Nicole M. Deming, Donna L. Luebke, Miriam Weiss, Rachel Phetteplace & Stuart J. Youngner (2014). Ethics Without Borders? Why The United States Needs an International Dialogue on Living Organ Donation. In Akira Akabayashi (ed.), The Future of Bioethics: International Dialogues. Oup Oxford.
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  4. Anita L. Allen, Stephen Bates, Mark A. Bedau, Jessica Berg, Nicole Deming, Ryan Blum, Benjamin Boltin, Nancy Berlinger, Harold Braswell & Daniel Callahan (2011). Following is the Comprehensive Index for Volume 41 of the Hastings Center Report, Covering All Feature Material From 2011. Letters Have Not Been Included. Ffl Complete Issues Are Available for Volume 41 (2011) and May Be Purchased From Wiley-Blackwell; E-Mail: Cs-Journals@ Wiley. Com. [REVIEW] Hastings Center Report 41.
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  5. Jessica Berg & Nicole Deming (2011). New Rules for Research with Human Participants? Hastings Center Report 41 (6):10-11.
    In July, the Department of Health and Human Services and the Office of Science and Technology Policy published an advance notice of proposed rulemaking proposing sweeping changes to the rules governing oversight of research on human subjects—changes aimed at “better protect[ing] human subjects who are involved in research, while facilitating valuable research and reducing burden, delay, and ambiguity for investigators.”1 The process is likely to amend not only the core regulation on human-subjects research , but also regulations governing vulnerable subjects, (...)
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