dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversity of São Camilo
dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.contributorGraduate School of Health Sciences
dc.date.accessioned2014-05-27T11:22:49Z
dc.date.available2014-05-27T11:22:49Z
dc.date.created2014-05-27T11:22:49Z
dc.date.issued2008-03-01
dc.identifierJournal International de Bioethique, v. 19, n. 1-2, p. 131-141, 2008.
dc.identifier1145-0762
dc.identifierhttp://hdl.handle.net/11449/70336
dc.identifier2-s2.0-48849110963
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.
dc.languageeng
dc.relationJournal International de Bioethique
dc.rightsAcesso restrito
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 subjects
dc.typeArtículos de revistas


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