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Contemporary Clinical Trials|May 15, 2012
Commonly performed procedures in clinical research: a benchmark for paymentDinora Dominguez, Mandy Jawara, Nicole Martino, et al.Journal of Medical Ethics|February 9, 2012
The quality of informed consent: mapping the landscape. A review of empirical data from developing and developed countriesAmulya Mandava, Christine Pace, Benjamin Campbell, et al.Nature Reviews. Immunology|March 27, 2002
Ethics of clinical research in the developing worldJack Killen, Christine Grady, Gregory K Folkers, 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.The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|May 28, 2026
Replacing Surrogate Decision-Making with Supported Decision-Making for Minimal Risk ResearchJennifer Hawkins, Aaron Eli Segal, David Wendler, et al.The Journal of Law, Medicine & Ethics : a Journal of the American Society of Law, Medicine & Ethics|December 6, 2006
The limits of disclosure: what research subjects want to know about investigator financial interestsChristine Grady, Elizabeth Horstmann, Jeffrey S Sussman, et al.Contemporary Clinical Trials|May 25, 2005
An analysis of U.S. practices of paying research participantsChristine Grady, Neal Dickert, Tom Jawetz, et al.Journal of Public Health Policy|March 31, 2022
The ethics of encouraging employees to get the COVID-19 vaccinationBenjamin E Berkman, Skye A Miner, David S Wendler, et al.JAMA|August 18, 2005
Quantifying the federal minimal risk standard: implications for pediatric research without a prospect of direct benefitDavid Wendler, Leah Belsky, Kimberly M Thompson, et al.Pageof 26