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British Journal of Clinical Pharmacology|January 9, 2016
The potential exploitation of research participants in high income countries who lack access to health careRafael Dal-Ré, Annette Rid, Ezekiel Emanuel, et al.
Clinical Trials (London, England)|September 10, 2015
Risks of phase I research with healthy participants: A systematic reviewRebecca A Johnson, Annette Rid, Ezekiel Emanuel, et al.
Archives of Internal Medicine|June 25, 2008
Why patients continue to participate in clinical researchDavid Wendler, Benjamin Krohmal, Ezekiel J Emanuel, et al.
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|May 28, 2026
Replacing Surrogate Decision-Making with Supported Decision-Making for Minimal Risk ResearchJennifer Hawkins, Aaron Eli Segal, David Wendler, et al.
JAMA|August 18, 2005
Quantifying the federal minimal risk standard: implications for pediatric research without a prospect of direct benefitDavid Wendler, Leah Belsky, Kimberly M Thompson, et al.
JAMA|January 30, 2004
How do institutional review boards apply the federal risk and benefit standards for pediatric research?Seema Shah, Amy Whittle, Benjamin Wilfond, et al.
Archives of Internal Medicine|April 28, 2010
Is emergency research without initial consent justified?: the consent substitute modelEmily A Largent, David Wendler, Ezekiel Emanuel, et al.
British Journal of Clinical Pharmacology|April 19, 2017
Public preferences on written informed consent for low-risk pragmatic clinical trials in SpainRafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
AIDS (London, England)|November 16, 2010
Empirical evaluation of the need for 'on-going consent' in clinical researchWilliam Smith, Christine Grady, Benjamin Krohmal, et al.
BMC Medical Research Methodology|September 20, 2017
Patients' beliefs regarding informed consent for low-risk pragmatic trialsRafael Dal-Ré, Antonio J Carcas, Xavier Carné, et al.
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