Design and implementation of community consultation for research conducted under exception from informed consent regulations for the PreVent and the PreVent 2 trials: Changes over time and during the COVID-19 pandemic
Author:
Affiliation:
1. Yale University, New Haven, CT, USA
2. University of Washington, Seattle, WA, USA
3. Duke University, Durham, NC, USA
4. Department of Anesthesiology, Duke University Medical Center, Duke University, Durham, NC, USA
Abstract
Funder
National Institute of Health, National Heath, Lung, and Blood Institute
Publisher
SAGE Publications
Link
https://journals.sagepub.com/doi/pdf/10.1177/17407745241243045
Reference15 articles.
1. U.S. Food and Drug Administration. Title 21 CFR § 50.24 Protection of human subjects, https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=50.24 (1996, accessed 24 March 2023)
2. Does Community Consultation Matter?
3. U.S. Food and Drug Administration. Guidance for institutional review boards, clinical investigators, and sponsors; Exception from informed consent requirements for emergency research. Final guidance, http://www.fda.gov/downloads/RegulatoryInformation/Guidances/UCM249673.pdf (2013, accessed 24 March 2023).
4. Community attitudes towards emergency research and exception from informed consent
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
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