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Journal of General Internal Medicine|January 15, 2015
"Targeted" consent for pragmatic clinical trialsDavid WendlerArchives of Pediatrics & Adolescent Medicine|February 4, 2009
Minimal risk in pediatric research as a function of ageDavid WendlerJournal of Medical Ethics|February 6, 2010
Are physicians obligated always to act in the patient's best interests?David WendlerTheoretical Medicine and Bioethics|March 21, 2014
Should protections for research with humans who cannot consent apply to research with nonhuman primates?David WendlerBioethics|August 12, 2020
Informed consent for controlled human infection studies in low- and middle-income countries: Ethical challenges and proposed solutionsVina Vaswani, Abha Saxena, Seema K Shah, et al.Plos Medicine|August 8, 2018
Choices in vaccine trial design in epidemics of emerging infectionsRebecca Kahn, Annette Rid, Peter G Smith, et al.Clinical Trials (London, England)|December 10, 2025
Charting the content of data monitoring committee charters for clinical trialsLisa Eckstein, Akram Ibrahim, Olivia Orr, et al.Archives of Pediatrics & Adolescent Medicine|January 9, 2008
Children's and their parents' views on facing research risks for the benefit of othersDavid Wendler, Tammara JenkinsVaccine|February 27, 2025
Assessing the risks of current COVID-19 challenge trials systematicallyNir Eyal, David WendlerInternal Medicine Journal|December 23, 2020
Ethics of information-gathering interventions in innovative practiceJake Earl, David WendlerPageof 20