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BMJ (Clinical Research Ed.)
|
March 4, 2006
One-time general consent for research on biological samples
David Wendler
Theoretical Medicine and Bioethics
|
March 15, 2011
What we worry about when we worry about the ethics of clinical research
David Wendler
Clinical Trials (London, England)
|
December 19, 2017
Innovative approaches to informed consent for randomized clinical trials: Identifying the ethical challenges
David Wendler
Journal of General Internal Medicine
|
January 27, 2021
The Ethics of Mandatory Retention of Clinical Biospecimens for Research
David 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 Requirement
David Wendler
The Hastings Center Report
|
January 12, 2017
The Theory and Practice of Surrogate Decision-Making
David Wendler
Kennedy Institute of Ethics Journal
|
November 7, 2022
Suffering in Animal Research: The Need for Limits and the Possibility of Compensation
David 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
Page
of 22
Search research articles
Search
Showing results (21-30 of 214) with videos related to
Sort By:
Page
of 22
BMJ (Clinical Research Ed.)
|
March 4, 2006
One-time general consent for research on biological samples
David Wendler
Theoretical Medicine and Bioethics
|
March 15, 2011
What we worry about when we worry about the ethics of clinical research
David Wendler
Clinical Trials (London, England)
|
December 19, 2017
Innovative approaches to informed consent for randomized clinical trials: Identifying the ethical challenges
David Wendler
Journal of General Internal Medicine
|
January 27, 2021
The Ethics of Mandatory Retention of Clinical Biospecimens for Research
David 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 Requirement
David Wendler
The Hastings Center Report
|
January 12, 2017
The Theory and Practice of Surrogate Decision-Making
David Wendler
Kennedy Institute of Ethics Journal
|
November 7, 2022
Suffering in Animal Research: The Need for Limits and the Possibility of Compensation
David 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
Page
of 22