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Clinical Trials (London, England)|February 25, 2016
Research involving pediatric stem cell donors: A way forwardDavid Wendler, Nirali N Shah, Michael A Pulsipher, et al.Annals of Internal Medicine|July 29, 2015
Pragmatic Randomized Trials Without Standard Informed Consent?: A National SurveyRahul K Nayak, David Wendler, Franklin G Miller, et al.Journal of Child and Adolescent Psychopharmacology|September 12, 2014
Evaluating the risks of clinical research: direct comparative analysisAnnette Rid, Emily Abdoler, Roxann Roberson-Nay, et al.Clinical Trials (London, England)|September 17, 2015
Considerations in the evaluation and determination of minimal risk in pragmatic clinical trialsJohn D Lantos, David Wendler, Edward Septimus, et al.Journal of Empirical Research on Human Research Ethics : JERHRE|September 17, 2009
Benefits and burdens of participation in a longitudinal clinical trialJaime Lazovski, Marcelo Losso, Benjamin Krohmal, et al.Critical Care Medicine|August 11, 2016
Targeted Consent for Research on Standard of Care Interventions in the Emergency SettingDavid Wendler, Neal W Dickert, Robert Silbergleit, et al.Prenatal Diagnosis|May 4, 2022
A new ethical framework to determine acceptable risks in fetal therapy trialsSaskia Hendriks, Christine Grady, David Wasserman, et al.Asian Bioethics Review|February 3, 2025
Review Mechanisms for Advanced Medical Therapies in Japan and Thailand: A Proposal for the Use of Expert Clinical Benefit Assessments at Designated InstitutionsKenji Matsui, Nipan Israsena, Jaranit Kaewkungwal, et al.Healthcare Policy = Politiques De Sante|March 30, 2018
Research on Human Embryos and Reproductive Materials: Revisiting Canadian Law and PolicyUbaka Ogbogu, Amy Zarzeczny, Jay Baltz, et al.BMJ (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.Pageof 24