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Ethics & Human Research|May 19, 2020
IRB Policies for Obtaining Informed Consent from Non-English-Speaking PeopleGianna McMillanEthics & Human Research|November 2, 2020
Loopholes in the Research Ethics System? Informed Consent Waivers in Cluster Randomized Trials with Individual-Level InterventionAlex John London, Monica Taljaard, Charles WeijerEthics & Human Research|January 23, 2020
When IRBs Say No to Participating in Research about Single IRBsRobert Klitzman, Paul S Appelbaum, Alexandra Murray, et al.Ethics & Human Research|February 13, 2019
Public Comments on the Proposed Common Rule Mandate for Single-IRB Review of Multisite ResearchHolly A Taylor, Stephan Ehrhardt, Ann-Margret ErvinEthics & Human Research|February 13, 2019
Reviving Human Research in Costa RicaMichael Householder, Ana Laura Solano-López, Derby Muñóz-Rojas, et al.Ethics & Human Research|July 1, 2021
An Argument for Reinterpreting the Benign Behavioral Intervention ExemptionIan TullyEthics & Human Research|September 16, 2020
Person-Oriented Research Ethics to Address the Needs of Participants on the Autism SpectrumM Ariel Cascio, Jonathan A Weiss, Eric RacineEthics & Human Research|January 19, 2021
What Factors Predict Willingness to Join Low-Risk Pragmatic Clinical Trials?Stephanie R Morain, Nancy E Kass, Ruth R FadenEthics & Human Research|January 19, 2021
Should the Regulation of Research Misconduct Be Integrated with the Ethics Framework Promulgated in The Belmont Report?Barbara K Redman, Arthur L CaplanEthics & Human Research|January 19, 2021
Should Participants in Clinical Trials Be Able to Withdraw from Passive Follow-Up?Warren H Capell, Matthew K Wynia, Elisa A Hurley, et al.Pageof 20