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David Wendler

Showing results (11-20 of 214) with videos related to

Pageof 22
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JAMA|April 21, 2011
How to enroll participants in research ethicallyDavid Wendler
Clinical Trials (London, England)|August 19, 2020
When and how to include vulnerable subjects in clinical trialsDavid Wendler
The Hastings Center Report|December 27, 2018
Locating the Source(s) of the Social Value Requirement(s)David Wendler
Kennedy Institute of Ethics Journal|July 30, 2004
Risk standards for pediatric research: rethinking the Grimes rulingDavid Wendler
The American Journal of Bioethics : AJOB|August 16, 2014
Justice and nontherapeutic pediatric researchDavid Wendler
Bioethics|August 9, 2017
A pragmatic analysis of vulnerability in clinical researchDavid Wendler
Perspectives in Biology and Medicine|January 8, 2021
Minimizing Risks Is Not Enough: The Relevance of Benefits to Protecting Research ParticipantsDavid Wendler
JAMA|June 23, 2022
Promoting the Values for Surrogate Decision-makingDavid Wendler
Annals of Internal Medicine|April 18, 2012
Consent for research with biological samples: one-time general consent versus a gift modelDavid Wendler
Archives of Internal Medicine|November 10, 2004
Can we ensure that all research subjects give valid consent?David Wendler
Pageof 22

Showing results (11-20 of 214) with videos related to

Sort By:
Pageof 22
JAMA|April 21, 2011
How to enroll participants in research ethicallyDavid Wendler
Clinical Trials (London, England)|August 19, 2020
When and how to include vulnerable subjects in clinical trialsDavid Wendler
The Hastings Center Report|December 27, 2018
Locating the Source(s) of the Social Value Requirement(s)David Wendler
Kennedy Institute of Ethics Journal|July 30, 2004
Risk standards for pediatric research: rethinking the Grimes rulingDavid Wendler
The American Journal of Bioethics : AJOB|August 16, 2014
Justice and nontherapeutic pediatric researchDavid Wendler
Bioethics|August 9, 2017
A pragmatic analysis of vulnerability in clinical researchDavid Wendler
Perspectives in Biology and Medicine|January 8, 2021
Minimizing Risks Is Not Enough: The Relevance of Benefits to Protecting Research ParticipantsDavid Wendler
JAMA|June 23, 2022
Promoting the Values for Surrogate Decision-makingDavid Wendler
Annals of Internal Medicine|April 18, 2012
Consent for research with biological samples: one-time general consent versus a gift modelDavid Wendler
Archives of Internal Medicine|November 10, 2004
Can we ensure that all research subjects give valid consent?David Wendler
Pageof 22