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dc.contributor.authorDoshi, Peter
dc.contributor.authorGodlee, Fiona
dc.date.accessioned2017-05-25T01:11:16Z
dc.date.available2017-05-25T01:11:16Z
dc.date.issued2017-04-27
dc.identifier.citationDoshi, P. & Godlee, F. (2017). The wider role of regulatory scientists. BMJ, 357. DOI: 10.1136/bmj.j1991
dc.identifier.urihttp://hdl.handle.net/10713/6593
dc.descriptionSubtitle: Why they must help us improve the evidence base; Editorial in which the authors discuss drug clinical trial data submitted to the US Food and Drug Administration and call for regulators to correct misleading information published in the medical literature.
dc.description.urihttp://bmj.com/cgi/content/full/bmj.j1991?ijkey=BpVIzvF15k4WHLc&keytype=ref
dc.language.isoen_USen_US
dc.publisherBMJ Publishing Groupen_US
dc.subjectethical responsibility of regulatory scientistsen_US
dc.subject.meshAccess to Informationen_US
dc.subject.meshClinical Trials as Topicen_US
dc.subject.meshDisclosureen_US
dc.subject.meshSocial Responsibilityen_US
dc.subject.meshUnited States. Food and Drug Administration--ethicsen_US
dc.titleThe wider role of regulatory scientistsen_US
dc.typeArticleen_US
dc.identifier.doi10.1136/bmj.j1991
dc.identifier.pmid28450290
dc.identifier.ispublishedNoen_US
dc.description.urinameClick here for the free full-text article on publisher’s websiteen_US
refterms.dateFOA2019-02-19T18:15:40Z


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