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dc.creatorKuehn, Bridget Men
dc.date.accessioned2016-01-09T00:40:46Zen
dc.date.available2016-01-09T00:40:46Zen
dc.date.created2010-08-11en
dc.date.issued2010-08-11en
dc.identifierdoi:10.1001/jama.2010.1080en
dc.identifier.bibliographicCitationJAMA : the journal of the American Medical Association 2010 Aug 11; 304(6): 627en
dc.identifier.urihttp://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=IOM+advises+FDA+on+ethics+in+postmarket+safety+trials.&title=JAMA+:+the+journal+of+the+American+Medical+Association+&volume=304&issue=6&date=2010-08&au=Kuehn,+Bridget+Men
dc.identifier.urihttp://dx.doi.org/10.1001/jama.2010.1080en
dc.identifier.urihttp://hdl.handle.net/10822/1021793en
dc.formatArticleen
dc.languageenen
dc.sourceeweb:333974en
dc.subjectEthicsen
dc.subject.classificationHuman Experimentation Policy Guidelines / Institutional Review Boardsen
dc.subject.classificationInformed Consent or Human Experimentationen
dc.titleIOM Advises FDA on Ethics in Postmarket Safety Trialsen
dc.provenanceCitation prepared by the Library and Information Services group of the Kennedy Institute of Ethics, Georgetown University for the ETHXWeb database.en
dc.provenanceCitation migrated from OpenText LiveLink Discovery Server database named EWEB hosted by the Bioethics Research Library to the DSpace collection EthxWeb hosted by DigitalGeorgetown.en


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