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David Wendler

Showing results (21-30 of 214) with videos related to

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BMJ (Clinical Research Ed.)|March 4, 2006
One-time general consent for research on biological samplesDavid Wendler
Theoretical Medicine and Bioethics|March 15, 2011
What we worry about when we worry about the ethics of clinical researchDavid Wendler
Clinical Trials (London, England)|December 19, 2017
Innovative approaches to informed consent for randomized clinical trials: Identifying the ethical challengesDavid Wendler
Journal of General Internal Medicine|January 27, 2021
The Ethics of Mandatory Retention of Clinical Biospecimens for ResearchDavid Wendler
IRB|January 21, 2014
Do U.S. regulations allow more than minor increase over minimal risk pediatric research? Should they?David Wendler
The Journal of Medicine and Philosophy|November 5, 2022
Deceiving Research Participants: Is It Inconsistent With Valid Consent?David Wendler
The American Journal of Bioethics : AJOB|May 25, 2016
The Potential for Infrastructure Benefits and the Responsiveness RequirementDavid Wendler
The Hastings Center Report|January 12, 2017
The Theory and Practice of Surrogate Decision-MakingDavid Wendler
Kennedy Institute of Ethics Journal|November 7, 2022
Suffering in Animal Research: The Need for Limits and the Possibility of CompensationDavid Wendler
Archives of Internal Medicine|July 26, 2006
One-time general consent for research on biological samples: is it compatible with the health insurance portability and accountability act?David Wendler
Pageof 22

Showing results (21-30 of 214) with videos related to

Sort By:
Pageof 22
BMJ (Clinical Research Ed.)|March 4, 2006
One-time general consent for research on biological samplesDavid Wendler
Theoretical Medicine and Bioethics|March 15, 2011
What we worry about when we worry about the ethics of clinical researchDavid Wendler
Clinical Trials (London, England)|December 19, 2017
Innovative approaches to informed consent for randomized clinical trials: Identifying the ethical challengesDavid Wendler
Journal of General Internal Medicine|January 27, 2021
The Ethics of Mandatory Retention of Clinical Biospecimens for ResearchDavid Wendler
IRB|January 21, 2014
Do U.S. regulations allow more than minor increase over minimal risk pediatric research? Should they?David Wendler
The Journal of Medicine and Philosophy|November 5, 2022
Deceiving Research Participants: Is It Inconsistent With Valid Consent?David Wendler
The American Journal of Bioethics : AJOB|May 25, 2016
The Potential for Infrastructure Benefits and the Responsiveness RequirementDavid Wendler
The Hastings Center Report|January 12, 2017
The Theory and Practice of Surrogate Decision-MakingDavid Wendler
Kennedy Institute of Ethics Journal|November 7, 2022
Suffering in Animal Research: The Need for Limits and the Possibility of CompensationDavid Wendler
Archives of Internal Medicine|July 26, 2006
One-time general consent for research on biological samples: is it compatible with the health insurance portability and accountability act?David Wendler
Pageof 22