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dc.contributor.authorLysaght, T
dc.contributor.authorKerridge, I
dc.contributor.authorSipp, D
dc.contributor.authorPorter, G
dc.contributor.authorCapps, BJ
dc.date.accessioned2016-05-16
dc.date.available2016-05-16
dc.date.issued2013-01-01
dc.identifier.citationLysaght T, Kerridge I, Sipp D, Porter G, Capps BJ. Oversight for clinical use of autologous adult stem cells: lessons from international regulations. Cell Stem Cell. 2013;13(6):647-51.en_AU
dc.identifier.urihttp://hdl.handle.net/2123/14921
dc.description.abstractAutologous adult stem cells (ASCs) are being administered by physicians for indications that have not been demonstrated as safe and effective in formal clinical trials. Examination of regulatory frameworks across five countries suggests that balancing the demands of research with clinical freedom has created structural weaknesses that are being exploited.en_AU
dc.description.sponsorshipfunded by the Ministry of Education, Singapore, and the Humanities and Social Sciences (HSS) Division of the Office of the Deputy President (Research and Technology) at the National University of Singapore (NUS).en_AU
dc.language.isoenen_AU
dc.publisherElsevieren_AU
dc.subjectAutologous adult stem cells (ASCs)en_AU
dc.subjectstem cellsen_AU
dc.subjectregulatory frameworksen_AU
dc.subjectclinical freedomen_AU
dc.titleOversight for clinical uses of autologous adult stem cells: lessons from international regulationsen_AU
dc.typeArticleen_AU


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