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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/70336
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dc.contributor.authorSaad Hossne, William-
dc.contributor.authorVieira, Sonia-
dc.contributor.authorBontempo Duca de Freitas, Corina-
dc.date.accessioned2014-05-27T11:22:49Z-
dc.date.accessioned2016-10-25T18:25:19Z-
dc.date.available2014-05-27T11:22:49Z-
dc.date.available2016-10-25T18:25:19Z-
dc.date.issued2008-03-01-
dc.identifierhttp://europepmc.org/abstract/MED/18664006-
dc.identifier.citationJournal International de Bioethique, v. 19, n. 1-2, p. 131-141, 2008.-
dc.identifier.issn1145-0762-
dc.identifier.urihttp://hdl.handle.net/11449/70336-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/70336-
dc.description.abstractIn Brazil since October 1996 there have been guidelines for research involving human subjects. Now human subjects know when their treatment is part of research. Deceit is no longer tolerated. But is not enough to say we offer an explanation to the potential subject and we offer a choice before he or she is confronted with an informed consent form. As in all professional activity, scientific investigation needs social controls. In Brazil, the ultimate responsibility of an investigation lies on the investigator, but in every institution where research is carried out there is a Committee for Ethics in Research. All Committees are subordinated to the National Commission of Ethics in Research, which is submitted to the Brazilian Institute of Health. During 2005 around 17,000 protocols involving 700,000 human subjects were revised by 475 Committees distributed all over the country. Approximately 7,000 people are now working in these Committees.en
dc.format.extent131-141-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBrazil-
dc.subjectClinical trial-
dc.subjectPractice guidelines-
dc.subjectResearch ethics committes-
dc.subjectResearch subjects-
dc.subjectbioethics-
dc.subjectclinical trial-
dc.subjectdoctor patient relation-
dc.subjectdrug industry-
dc.subjectethics-
dc.subjecthuman-
dc.subjecthuman experiment-
dc.subjecthuman relation-
dc.subjectinformed consent-
dc.subjectorganization and management-
dc.subjectpatient right-
dc.subjectpatient selection-
dc.subjectpractice guideline-
dc.subjectprofessional standard-
dc.subjectpublic health-
dc.subjectresearch ethics-
dc.subjectBioethical Issues-
dc.subjectClinical Trials as Topic-
dc.subjectDrug Industry-
dc.subjectEthics Committees, Research-
dc.subjectEthics, Research-
dc.subjectGuidelines as Topic-
dc.subjectHuman Experimentation-
dc.subjectHumans-
dc.subjectInformed Consent-
dc.subjectNational Health Programs-
dc.subjectPatient Rights-
dc.subjectPatient Selection-
dc.subjectPhysician-Patient Relations-
dc.subjectResearcher-Subject Relations-
dc.titleCommittees for ethics in research involving human subjectsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversity of São Camilo-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionGraduate School of Health Sciences-
dc.description.affiliationEmeritus Botucatu Medical School UNESP Sao Paulo State University, São Paulo-
dc.description.affiliationUniversity of São Camilo, Sã Paulo-
dc.description.affiliationState University of Campinas, São Paulo-
dc.description.affiliationGraduate School of Health Sciences-
dc.description.affiliationUnespEmeritus Botucatu Medical School UNESP Sao Paulo State University, São Paulo-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal International de Bioethique-
dc.identifier.scopus2-s2.0-48849110963-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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