Protection of human subjects in research trials.
Horrors of medical experiments done on prisoners in concentration camps during World War II led to the Nuremberg Code, the basis of the present day informed consent process. Informed consent requires that subjects in research projects be fully informed of the risks and benefits of the trial, that th...
| Publicado en: | American Journal of Electroneurodiagnostic Technology Vol. 43; no. 2; pp. 54 - 63 |
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| Autor principal: | |
| Formato: | CEU exam questions Journal Article |
| Publicado: |
Taylor & Francis Ltd
Jun2003
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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=ccm&AN=106785049&site=ehost-live header: @attributes: shortDbName: ccm uiTerm: 106785049 longDbName: CINAHL Complete uiTag: AN controlInfo: bkinfo: dissinfo: jinfo: jid: 1086508X GJ9 jtl: American Journal of Electroneurodiagnostic Technology issn: 1086508X maglogo: N pubinfo: dt: Jun2003 vid: 43 iid: 2 pid: 377 pub: Taylor & Francis Ltd place: Philadelphia, Pennsylvania artinfo: ui: 106785049 106785049 2003160929 10.1080/1086508x.2003.11079420 106785049 ppf: 54 ppct: 9 formats: fmt: @attributes: type: P tig: atl: Protection of human subjects in research trials. aug: au: York DH affil: Director of Neuroscience, St. John's Mercy Medical Center, 615 S. New Ballas Road, St. Louis, MO 63141 sug: subj: Consent Research Ethics Education, Continuing (Credit) Risk Assessment Vulnerability World Wide Web ab: Horrors of medical experiments done on prisoners in concentration camps during World War II led to the Nuremberg Code, the basis of the present day informed consent process. Informed consent requires that subjects in research projects be fully informed of the risks and benefits of the trial, that they participate freely, and that their well-being be safeguarded throughout the course of the experiment. Experimental treatment must be clearly defined as research. All research in the U.S. must be approved by an Institutional Review Board (IRB) before it starts, and all investigators receiving federal support must receive training in the regulations and ethics of human experimentation. The regulations and opportunities for training are available on the World Wide Web. pubtype: Academic Journal doctype: CEU exam questions Journal Article ougenre: Article language: English refInfo: holdings: @attributes: islocal: N |
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