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Plos Medicine|May 25, 2006
Does random treatment assignment cause harm to research participants?Cary P Gross, Harlan M Krumholz, Gretchen Van Wye, et al.BMC Medical Ethics|June 21, 2017
Comparative effectiveness research: what to do when experts disagree about risksReidar K Lie, Francis K L Chan, Christine Grady, et al.The Lancet. Infectious Diseases|June 9, 2023
A partner protection package for HIV cure-related trials involving analytical treatment interruptionsKarine Dubé, Tia Morton, Lawrence Fox, et al.Vaccine|September 28, 2020
Integrating public health programs and research after the malaria vaccine implementation program (MVIP): Recommendations for next stepsRieke van der Graaf, Ruth Macklin, Annette Rid, et al.Journal of the American Geriatrics Society|July 10, 2021
Resources, methods, and data infrastructure to promote research in dementia care, caregiving, and servicesK Joanne Pike, Sam Fazio, Julie P W Bynum, et al.Journal of Medical Ethics|April 1, 2015
Research led by participants: a new social contract for a new kind of researchEffy Vayena, Roger Brownsword, Sarah Jane Edwards, et al.AJOB Empirical Bioethics|March 8, 2022
Surrogate Perspectives on Patient Preference Predictors: Good Idea, but I Should Decide How They Are UsedDana Howard, Allan Rivlin, Philip Candilis, et al.Journal of Health Organization and Management|July 30, 2016
Public participation in decision-making on the coverage of new antivirals for hepatitis CKatharina Kieslich, Jeonghoon Ahn, Gabriele Badano, et al.BMC Medical Ethics|July 11, 2018
Standards of practice in empirical bioethics research: towards a consensusJonathan Ives, Michael Dunn, Bert Molewijk, et al.The Journal of Adolescent Health : Official Publication of the Society for Adolescent Medicine|March 18, 2014
Assent in research: the voices of adolescentsChristine Grady, Lori Wiener, Emily Abdoler, et al.Pageof 20