Trial participants' rights after authorisation of COVID-19 vaccines.
作者信息
Dal-Ré Rafael, Orenstein Walter, Caplan Arthur L
机构信息
Epidemiology Unit, Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid, E-28040 Madrid, Spain.
Division of Infectious Diseases, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA; Emory Vaccine Center, Emory University, Atlanta, GA, USA.
出版信息
Lancet Respir Med. 2021 Apr;9(4):e30-e31. doi: 10.1016/S2213-2600(21)00044-8. Epub 2021 Jan 18.
Abstract
摘要
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本文引用的文献
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Ethical and Scientific Considerations Regarding the Early Approval and Deployment of a COVID-19 Vaccine.关于 COVID-19 疫苗的早期批准和使用的伦理和科学考虑。
Ann Intern Med. 2021 Feb;174(2):258-260. doi: 10.7326/M20-7357. Epub 2020 Nov 20.
3
When should re-consent of subjects participating in a clinical trial be requested? A case-oriented algorithm to assist in the decision-making process.何时应要求参与临床试验的受试者重新签署知情同意书？一种以案例为导向的算法，以协助决策过程。
Clin Pharmacol Ther. 2008 May;83(5):788-93. doi: 10.1038/sj.clpt.6100357. Epub 2007 Sep 19.
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World Medical Association Declaration of Helsinki. Ethical principles for medical research involving human subjects.世界医学协会《赫尔辛基宣言》。涉及人类受试者的医学研究伦理原则。
Nurs Ethics. 2002 Jan;9(1):105-9. doi: 10.1191/0969733002ne486xx.
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