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dc.creatorMerrill, Richard A.en
dc.date.accessioned2016-01-08T21:18:04Zen
dc.date.available2016-01-08T21:18:04Zen
dc.date.created1996-11en
dc.date.issued1996-11en
dc.identifierdoi:10.2307/1073689en
dc.identifier.bibliographicCitationVirginia Law Review 1996 November; 82(8): 1753-1866en
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=The+architecture+of+government+regulation+of+medical+products&title=Virginia+Law+Review+&volume=82&issue=8&spage=1753-1866&date=1996-11&au=Merrill,+Richard+A.en
dc.identifier.urihttp://dx.doi.org/10.2307/1073689en
dc.identifier.urihttp://hdl.handle.net/10822/897575en
dc.formatArticleen
dc.languageenen
dc.sourceeweb:169222en
dc.subjectGovernmenten
dc.subjectGovernment Regulationen
dc.subjectRegulationen
dc.subject.classificationDrugs and Drug Industryen
dc.subject.classificationHuman Experimentation Policy Guidelines / Institutional Review Boardsen
dc.titleThe Architecture of Government Regulation of Medical Productsen
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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