Investigación biomédica, tratamiento de muestras genéticas humanas y biobancos

Autor:	Navarro Caballero, Teresa M.
Jazyk:	angličtina
Rok vydání:	2014
Předmět:	Ethics Law in general. Comparative and uniform law. Jurisprudence Investigación Derechos humanos K1-7720 Genética humana 340 - Cuestiones generales de derecho. Métodos y ciencias auxiliares del derecho BJ1-1725 Bioética biobanks genetic data medical research autonomy consent
Zdroj:	Bioderecho.es, Iss 1 (2014) DIGITUM. Depósito Digital Institucional de la Universidad de Murcia instname
ISSN:	2386-6594
Popis:	Biomedical research is fundamental to improving the quality and life expectancy of citizens and increase their welfare. The science´s progress results in the appearance of new analytical tools that creates hope for the treatment of untreatable pathology. However, the scientific-technological advances generate ethical and legal uncertainties that need to be regulated with prudence because affect human identity. It´s necessary to have a regulatory framework to defend the rights of the persons that participate in a biomedicine research. In Spain, the Law 14/2007, de Investigación Biomédica, proclaims the free autonomy to take part in a biomedicine research. This paper is a reflection on the indispensable consent to participate in that research, devoting special attention to treatment of the biological samples in biobanks. BioLaw Journal - Rivista di BioDiritto, N° 1 (2014)
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65c5b2e879a84b27c82c9201e83c26e1 https://revistas.um.es/bioderecho/article/view/209371 Zobrazit plný text záznamu