Why IRBs should protect bystanders in human research.
Many types of human research activities present risks and burdens to third parties (e.g., bystanders). Few human protection policies directly address the protection of research bystanders, though some address it in passing. In what follows, I re‐iterate reasons why bystanders are entitled to protect...
| Publicado en: | Bioethics Vol. 34; no. 9; pp. 933 - 937 |
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| Formato: | Artículo |
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Wiley-Blackwell
Nov2020
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| Acceso en línea: | Ver este registro en EBSCOhost |
| fields | @attributes: recordID: 1 pdfLink: plink: https://search.ebscohost.com/login.aspx?direct=true&db=ssf&AN=147132008&site=ehost-live header: @attributes: shortDbName: ssf uiTerm: 147132008 longDbName: Social Sciences Full Text (H.W. Wilson) uiTag: AN controlInfo: bkinfo: jinfo: jid: 02699702 6PJ jtl: Bioethics issn: 02699702 maglogo: Y pubinfo: dt: Nov2020 vid: 34 iid: 9 pid: 480 pub: Wiley-Blackwell artinfo: ui: 147132008 10.1111/bioe.12812 ppf: 933 ppct: 4 formats: tig: atl: Why IRBs should protect bystanders in human research. aug: au: Kimmelman, Jonathan affil: Studies of Translation, Ethics, and Medicine (STREAM), Department of Biomedical Ethics, McGill University, Montreal Quebec, , Canada su: Bioethics Medical research Research ethics Human research subjects Safety Institutional review boards sug: subj: Bioethics Medical research Research ethics Human research subjects Research and Development in the Physical, Engineering, and Life Sciences (except Biotechnology) Safety Institutional review boards keyword: bystanders ethics review IRB research ethics risk bystanders ethics review IRB research ethics risk ab: Many types of human research activities present risks and burdens to third parties (e.g., bystanders). Few human protection policies directly address the protection of research bystanders, though some address it in passing. In what follows, I re‐iterate reasons why bystanders are entitled to protections. I also argue that Institutional Review Boards (IRBs) are in the best position to signal to researchers and sponsors that bystanders should be protected in research. In some cases, IRB review would consist of evaluating bystander protection strategies directly; in other cases, this might entail merely certifying that another institutions, like a drug regulator, has taken adequate measures to protect the welfare of research bystanders. pubtype: Academic Journal doctype: Article src: R language: English refInfo: copyright: @attributes: flag: N holdings: @attributes: islocal: N |
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