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The Hastings Center Report|June 28, 2022
Setting Risk Limits and Ensuring Fairness in Learning Health CareDavid Wendler, Connor SullivanThe Journal of Medicine and Philosophy|February 22, 2014
Treatment decision making for incapacitated patients: is development and use of a patient preference predictor feasible?Annette Rid, David WendlerJournal of Empirical Research on Human Research Ethics : JERHRE|May 9, 2012
Using data to improve surrogate consent for clinical research with incapacitated adultsEmily Abdoler, David WendlerTheoretical Medicine and Bioethics|May 19, 2016
When clinical care is like research: the need for review and consentDavid Wendler, Rebecca JohnsonThe Journal of Medicine and Philosophy|February 16, 2017
Why is Coerced Consent Worse Than No Consent and Deceived Consent?David Wendler, Alan WertheimerArchives of Internal Medicine|September 12, 2007
Medical decision making for patients without surrogatesSumeeta Varma, David WendlerBioethics|November 15, 2006
Protecting communities in health research from exploitationSegun Gbadegesin, David WendlerThe Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|June 29, 2010
Interpretation of the subjects' condition requirement: a legal perspectiveSeema Shah, David WendlerClinical Trials (London, England)|August 24, 2011
A proposal and prototype for a Research Risk Repository to improve the protection of research participantsAnnette Rid, David WendlerThe Journal of Medicine and Philosophy|July 31, 2015
Involving Communities in Deciding What Benefits They Receive in Multinational ResearchDavid Wendler, Seema ShahPageof 15