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  1. Informed consent for MRI and fMRI research: Analysis of a sample of Canadian consent documents.Nicole Palmour, William Affleck, Emily Bell, Constance Deslauriers, Bruce Pike, Julien Doyon & Eric Racine - 2011 - BMC Medical Ethics 12 (1):1.
    BackgroundResearch ethics and the measures deployed to ensure ethical oversight of research (e.g., informed consent forms, ethics review) are vested with extremely important ethical and practical goals. Accordingly, these measures need to function effectively in real-world research and to follow high level standards.MethodsWe examined approved consent forms for Magnetic Resonance Imaging (MRI) and functional Magnetic Resonance Imaging (fMRI) studies approved by Canadian research ethics boards (REBs).ResultsWe found evidence of variability in consent forms in matters of physical and psychological risk reporting. (...)
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  • The Concept of Minimal Risk: The Need for Better Guidance on the Ethics Review Process.Kyoko Wada - 2011 - American Journal of Bioethics 11 (6):27 - 29.
    The American Journal of Bioethics, Volume 11, Issue 6, Page 27-29, June 2011.
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  • Regulating “Higher Risk, No Direct Benefit” Studies in Minors.Anna E. Westra, Jan M. Wit, Rám N. Sukhai & Inez D. de Beaufort - 2011 - American Journal of Bioethics 11 (6):29 - 31.
    The American Journal of Bioethics, Volume 11, Issue 6, Page 29-31, June 2011.
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