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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.Journal of Empirical Research on Human Research Ethics : JERHRE|March 6, 2015
Contrasting views of risk perception and influence of financial compensation between adolescent research participants and their parentsLori Wiener, Adrienne Viola, Benjamin S Wilfond, et al.The American Journal of Hospice & Palliative Care|October 17, 2023
The Ethics of Conscientious Objection to Teaching Physician-Assisted DeathNoah Berens, Margaret M Mahon, Katalin Roth, et al.Pageof 16