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JAMA|October 7, 2010
Evaluating the risks of clinical researchAnnette Rid, Ezekiel J Emanuel, David WendlerBMJ (Clinical Research Ed.)|June 28, 2015
Quantifying the risks of non-oncology phase I research in healthy volunteers: meta-analysis of phase I studiesEzekiel J Emanuel, Gabriella Bedarida, Kristy Macci, et al.Kennedy Institute of Ethics Journal|June 24, 2011
A framework for risk-benefit evaluations in biomedical researchAnnette Rid, David WendlerThe Journal of Medicine and Philosophy|February 15, 2014
Use of a patient preference predictor to help make medical decisions for incapacitated patientsAnnette Rid, David WendlerBioethics|January 7, 2017
In Defense of a Social Value Requirement for Clinical ResearchDavid Wendler, Annette RidClinical Trials (London, England)|August 24, 2011
A proposal and prototype for a Research Risk Repository to improve the protection of research participantsAnnette Rid, David WendlerThe Hastings Center Report|October 23, 2010
Can we improve treatment decision-making for incapacitated patients?Annette Rid, David WendlerAnnals of Internal Medicine|March 2, 2011
Systematic review: the effect on surrogates of making treatment decisions for othersDavid Wendler, Annette RidThe 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 WendlerJournal of the American Geriatrics Society|April 4, 2012
Systematic review: Individuals' goals for surrogate decision-makingBrenna Kelly, Annette Rid, David WendlerPageof 30