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dc.contributorDepartament de Salut
dc.contributor.authorComitè de Bioètica de Catalunya
dc.date.accessioned2016-07-14T09:00:23Z
dc.date.available2016-07-14T09:00:23Z
dc.date.issued2003-03
dc.identifier.citationComitè de Bioètica de Catalunya. Guia de recomanacions sobre el consentiment informat. Barcelona: Direcció General de Recursos Sanitaris; 2003.
dc.identifier.urihttps://hdl.handle.net/11351/2207
dc.descriptionPatient rights; Clinical Communication; Patient autonomy
dc.description.abstractThe recommendations guide of informed consent pretends to record that the degree of participation of people is based on the preliminary information which is required to help to reflect and assess the suitability of undergo healthcare interventions proposed. Consent must be done properly, not to mention that the ultimate goal is to involve patients in decisions that affect them and assume responsibilities. The aim is that the legal character of consent does not replace the possibility of communication, dialogue, understanding and shared decision-making that are the cornerstone of care.
dc.language.isocat
dc.publisherDirecció General de Recursos Sanitaris
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.sourceScientia
dc.subjectConsentiment informat (Dret mèdic)
dc.subjectBioètica - Dret i legislació
dc.subjectMetge i pacient
dc.subject.lccKKT3119.I54 G85 1997
dc.subject.meshInformed Consent
dc.subject.meshBioethics
dc.subject.meshPhysician-Patient Relations
dc.titleGuia de recomanacions sobre el consentiment informat
dc.typeinfo:eu-repo/semantics/report
dc.identifier.dlB. 15.860-2003
dc.subject.decsconsentimiento informado
dc.subject.decsbioética
dc.subject.decsrelaciones médico-paciente
dc.type.versioninfo:eu-repo/semantics/publishedVersion
dc.audienceProfessionals
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess


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