Retorno de la bioética en ensayos clínicos

Autores
Mainetti, José Alberto
Año de publicación
2003
Idioma
español castellano
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Biomedical research ethics is a hot topic in USA today as it used to be when it was born three decades ago. New procedures to preserve and protect the scientific integrity and the human subjects involved in clinical trials are the response to the increasing distrust in scientific protocols, which some times do not follow the orthodox ethical standards, and many a times have developed some harm to participants becoming a threat to national human research policies. The new scene of investigation associates both the academic knowledge and the private enterprise; though not a novelty it shows now an exceptional financial increment by the pharmaceutical and biotechnological industries. In this sense, the industry changes the financial support from the academic to the private medicine -of a profitable nature- grounded on intermediary organizations that manage clinical trials providing the access to hospitals, health professionals, and patients. The concern then lies on this approach to managing clinical trials as long as investigation quality and human subjects are involved, mainly as regards the conflict of economical interests that arise among professionals and "non institutional" revision committee members. The consequence is a proposal of new rules for the handling of those conflicts of interests and the encouragement of education in bioethics for clinical researchers and revision committee s members.
Facultad de Ciencias Médicas
Materia
Ciencias Médicas
bioética
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/10281

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spelling Retorno de la bioética en ensayos clínicosMainetti, José AlbertoCiencias MédicasbioéticaBiomedical research ethics is a hot topic in USA today as it used to be when it was born three decades ago. New procedures to preserve and protect the scientific integrity and the human subjects involved in clinical trials are the response to the increasing distrust in scientific protocols, which some times do not follow the orthodox ethical standards, and many a times have developed some harm to participants becoming a threat to national human research policies. The new scene of investigation associates both the academic knowledge and the private enterprise; though not a novelty it shows now an exceptional financial increment by the pharmaceutical and biotechnological industries. In this sense, the industry changes the financial support from the academic to the private medicine -of a profitable nature- grounded on intermediary organizations that manage clinical trials providing the access to hospitals, health professionals, and patients. The concern then lies on this approach to managing clinical trials as long as investigation quality and human subjects are involved, mainly as regards the conflict of economical interests that arise among professionals and "non institutional" revision committee members. The consequence is a proposal of new rules for the handling of those conflicts of interests and the encouragement of education in bioethics for clinical researchers and revision committee s members.Facultad de Ciencias Médicas2003-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf25-30http://sedici.unlp.edu.ar/handle/10915/10281spainfo:eu-repo/semantics/altIdentifier/url/http://revista.med.unlp.edu.ar/archivos/200309/articulo%20original%202.pdfinfo:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc/4.0/Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T10:50:59Zoai:sedici.unlp.edu.ar:10915/10281Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 10:50:59.478SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Retorno de la bioética en ensayos clínicos
title Retorno de la bioética en ensayos clínicos
spellingShingle Retorno de la bioética en ensayos clínicos
Mainetti, José Alberto
Ciencias Médicas
bioética
title_short Retorno de la bioética en ensayos clínicos
title_full Retorno de la bioética en ensayos clínicos
title_fullStr Retorno de la bioética en ensayos clínicos
title_full_unstemmed Retorno de la bioética en ensayos clínicos
title_sort Retorno de la bioética en ensayos clínicos
dc.creator.none.fl_str_mv Mainetti, José Alberto
author Mainetti, José Alberto
author_facet Mainetti, José Alberto
author_role author
dc.subject.none.fl_str_mv Ciencias Médicas
bioética
topic Ciencias Médicas
bioética
dc.description.none.fl_txt_mv Biomedical research ethics is a hot topic in USA today as it used to be when it was born three decades ago. New procedures to preserve and protect the scientific integrity and the human subjects involved in clinical trials are the response to the increasing distrust in scientific protocols, which some times do not follow the orthodox ethical standards, and many a times have developed some harm to participants becoming a threat to national human research policies. The new scene of investigation associates both the academic knowledge and the private enterprise; though not a novelty it shows now an exceptional financial increment by the pharmaceutical and biotechnological industries. In this sense, the industry changes the financial support from the academic to the private medicine -of a profitable nature- grounded on intermediary organizations that manage clinical trials providing the access to hospitals, health professionals, and patients. The concern then lies on this approach to managing clinical trials as long as investigation quality and human subjects are involved, mainly as regards the conflict of economical interests that arise among professionals and "non institutional" revision committee members. The consequence is a proposal of new rules for the handling of those conflicts of interests and the encouragement of education in bioethics for clinical researchers and revision committee s members.
Facultad de Ciencias Médicas
description Biomedical research ethics is a hot topic in USA today as it used to be when it was born three decades ago. New procedures to preserve and protect the scientific integrity and the human subjects involved in clinical trials are the response to the increasing distrust in scientific protocols, which some times do not follow the orthodox ethical standards, and many a times have developed some harm to participants becoming a threat to national human research policies. The new scene of investigation associates both the academic knowledge and the private enterprise; though not a novelty it shows now an exceptional financial increment by the pharmaceutical and biotechnological industries. In this sense, the industry changes the financial support from the academic to the private medicine -of a profitable nature- grounded on intermediary organizations that manage clinical trials providing the access to hospitals, health professionals, and patients. The concern then lies on this approach to managing clinical trials as long as investigation quality and human subjects are involved, mainly as regards the conflict of economical interests that arise among professionals and "non institutional" revision committee members. The consequence is a proposal of new rules for the handling of those conflicts of interests and the encouragement of education in bioethics for clinical researchers and revision committee s members.
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