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Clinical Trials (London, England)|October 25, 2021
Design of placebo-controlled randomized trials of anticancer agents: Ethical considerations based on a review of published trialsAdélaïde Doussau, Isha Agarwal, Tito Fojo, 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.
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.
Applied Nursing Research : ANR|March 12, 2014
The impact of ethics and work-related factors on nurse practitioners' and physician assistants' views on quality of primary healthcare in the United StatesConnie M Ulrich, Qiuping Pearl Zhou, Alexandra Hanlon, et al.
The American Journal of Bioethics : AJOB|September 30, 2005
The limitations of "vulnerability" as a protection for human research participantsCarol Levine, Ruth Faden, Christine Grady, et al.
Neuron|August 15, 2023
Continuing trial responsibilities for implantable neural devicesSaskia Hendriks, Nina Hsu, Andrea C Beckel-Mitchener, et al.
Prehospital Emergency Care|July 12, 2023
"It's Pretty Sad If You Get Used to It": A Qualitative Study of First Responder Experiences with Opioid Overdose EmergenciesKyle Patch, Caroline Huang, Saskia Hendriks, et al.
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