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Archives of Internal Medicine|November 10, 2004
Can we ensure that all research subjects give valid consent?David WendlerTheoretical Medicine and Bioethics|March 15, 2011
What we worry about when we worry about the ethics of clinical researchDavid WendlerClinical Trials (London, England)|August 19, 2020
When and how to include vulnerable subjects in clinical trialsDavid WendlerThe Hastings Center Report|December 27, 2018
Locating the Source(s) of the Social Value Requirement(s)David WendlerKennedy Institute of Ethics Journal|July 30, 2004
Risk standards for pediatric research: rethinking the Grimes rulingDavid WendlerPerspectives in Biology and Medicine|January 8, 2021
Minimizing Risks Is Not Enough: The Relevance of Benefits to Protecting Research ParticipantsDavid WendlerThe Journal of Medicine and Philosophy|November 5, 2022
Deceiving Research Participants: Is It Inconsistent With Valid Consent?David WendlerThe Hastings Center Report|January 12, 2017
The Theory and Practice of Surrogate Decision-MakingDavid WendlerKennedy Institute of Ethics Journal|November 7, 2022
Suffering in Animal Research: The Need for Limits and the Possibility of CompensationDavid WendlerPageof 24