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Internal Medicine Journal|December 23, 2020
Ethics of information-gathering interventions in innovative practiceJake Earl, David WendlerAccountability in Research|January 28, 2025
Reflections on the 2024 Final Rule on Public Health Service Policies on Research MisconductTrisha Phillips, Jake EarlAJOB Empirical Bioethics|September 26, 2017
Do Patients Want their Families or their Doctors to Make Treatment Decisions in the Event of Incapacity, and Why?David Wendler, Robert Wesley, Mark Pavlick, et al.Journal of Medical Ethics|January 31, 2016
A new method for making treatment decisions for incapacitated patients: what do patients think about the use of a patient preference predictor?David Wendler, Bob Wesley, Mark Pavlick, et al.Journal of Medical Ethics|June 25, 2014
Prisoners as research participants: current practice and attitudes in the UKAnna Charles, Annette Rid, Hugh Davies, et al.British Journal of Clinical Pharmacology|January 9, 2016
The potential exploitation of research participants in high income countries who lack access to health careRafael Dal-Ré, Annette Rid, Ezekiel Emanuel, et al.Clinical Trials (London, England)|September 10, 2015
Risks of phase I research with healthy participants: A systematic reviewRebecca A Johnson, Annette Rid, Ezekiel Emanuel, et al.Journal of Medical Ethics|January 11, 2025
Ethical considerations for referral partnerships in clinical researchIsabella Li, Aisha T Langford, Christine Grady, et al.Bioethics|September 18, 2014
Clinical Trial Design for HIV Prevention Research: Determining Standards of PreventionLiza Dawson, Sheryl ZwerskiClinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|March 24, 2021
The Essential Role of Data and Safety Monitoring Boards (DSMBs) in Ensuring the Ethics of Global Vaccine Trials to Address Coronavirus Disease 2019 (COVID-19O)Lisa Eckstein, Annette Rid, Dorcas Kamuya, et al.Pageof 10