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Swiss Medical Weekly
|
June 7, 2013
Note of clarification concerning our article: controversies in the determination of death: perspectives from Switzerland
Annette Rid, Settimio Monteverde
Social Justice Research
|
July 9, 2019
Innovation as a value in healthcare priority-setting: the UK experience
Victoria Charlton, Annette Rid
Bioethics
|
January 7, 2017
In Defense of a Social Value Requirement for Clinical Research
David Wendler, Annette Rid
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
May 8, 2010
The 2008 Declaration of Helsinki - first among equals in research ethics?
Annette Rid, Harald Schmidt
Clinical Trials (London, England)
|
August 24, 2011
A proposal and prototype for a Research Risk Repository to improve the protection of research participants
Annette Rid, David Wendler
The Hastings Center Report
|
October 23, 2010
Can we improve treatment decision-making for incapacitated patients?
Annette Rid, David Wendler
Annals of Internal Medicine
|
March 2, 2011
Systematic review: the effect on surrogates of making treatment decisions for others
David Wendler, Annette Rid
Journal of Medical Ethics
|
October 30, 2014
Can informed consent to research be adapted to risk?
Danielle Bromwich, Annette Rid
Bioethics
|
August 27, 2020
Judging the social value of controlled human infection studies
Annette Rid, Meta Roestenberg
The 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 Wendler
Page
of 10
Search research articles
Search
Showing results (11-20 of 94) with videos related to
Sort By:
Page
of 10
Swiss Medical Weekly
|
June 7, 2013
Note of clarification concerning our article: controversies in the determination of death: perspectives from Switzerland
Annette Rid, Settimio Monteverde
Social Justice Research
|
July 9, 2019
Innovation as a value in healthcare priority-setting: the UK experience
Victoria Charlton, Annette Rid
Bioethics
|
January 7, 2017
In Defense of a Social Value Requirement for Clinical Research
David Wendler, Annette Rid
The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics
|
May 8, 2010
The 2008 Declaration of Helsinki - first among equals in research ethics?
Annette Rid, Harald Schmidt
Clinical Trials (London, England)
|
August 24, 2011
A proposal and prototype for a Research Risk Repository to improve the protection of research participants
Annette Rid, David Wendler
The Hastings Center Report
|
October 23, 2010
Can we improve treatment decision-making for incapacitated patients?
Annette Rid, David Wendler
Annals of Internal Medicine
|
March 2, 2011
Systematic review: the effect on surrogates of making treatment decisions for others
David Wendler, Annette Rid
Journal of Medical Ethics
|
October 30, 2014
Can informed consent to research be adapted to risk?
Danielle Bromwich, Annette Rid
Bioethics
|
August 27, 2020
Judging the social value of controlled human infection studies
Annette Rid, Meta Roestenberg
The 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 Wendler
Page
of 10