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dc.date.accessioned2016-01-09T00:12:13Zen
dc.date.available2016-01-09T00:12:13Zen
dc.date.created2003-03en
dc.date.issued2003-03en
dc.identifier.bibliographicCitationLondon: Medicines and Healthcare Products Regulatory Agency 2003; 19p. [Online]. Available: http://www.mhra.gov.uk/inforesources/publications/mlx287/content. pdf [2004 December 8]en
dc.identifier.urihttp://www.worldcat.org/search?q=ti%3ADraft+guidance+on+consent+by+a+legal+representative+on+behalf+of+a+person+not+able+to+consent+under+the+Medicines+for+Human+Use+Regulations+2003&qt=advanceden
dc.identifier.urihttp://hdl.handle.net/10822/1001878en
dc.languageenen
dc.publisherGreat Britain. Department of Health; Medicines and Healthcare Products Regulatory Agency (Great Britain)en
dc.sourceeweb:258087en
dc.subjectClinical Trialsen
dc.subjectConsenten
dc.subject.classificationInformed Consent or Human Experimentationen
dc.subject.classificationResearch on Newborns and Minorsen
dc.subject.classificationResearch on Mentally Disabled Personsen
dc.titleDraft Guidance on Consent by a Legal Representative on Behalf of a Person Not Able to Consent Under the Medicines for Human Use (Clinical Trials) Regulations 2003en
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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