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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.
Pediatrics|June 3, 2004
Institutional review board practices regarding assent in pediatric researchAmy Whittle, Seema Shah, Benjamin Wilfond, et al.
The American Journal of Bioethics : AJOB|June 30, 2017
A Proposed Process for Reliably Updating the Common RuleBenjamin E Berkman, David Wendler, Haley K Sullivan, et al.
AJOB Empirical Bioethics|March 23, 2016
Adolescent Research Participants' Descriptions of Medical ResearchChristine Grady, Isabella Nogues, Lori Wiener, et al.
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