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Toward a Legal-Ethical Framework for Regulating Human Genetic Information in Vulnerable Populations: An Issue of Justice

  • Maria Graciela de Ortúzar
Published/Copyright: February 13, 2009
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Journal of international biotechnology law
From the journal Volume 6 Issue 1

Abstract

The main purpose of this work is to discuss the legal, psycho-social and ethical issues posed when handling genetic information in genomic research within developing countries. Following the method of “reflective equilibrium”(Rawls-Daniels) and from an interdisciplinary approach, I shall go through: (1) current normative laws concerning its regulation, advantages and limitations; (2) the psychosocial impact of genetics on health issues; and (3) the ethical grounds that should be taken into account in establishing the normative framework for the regulation of genetic information. In general terms, my opinion is that the ethical grounds of the normative framework regarding research with human beings cannot be formal or based exclusively on the law (e. g. “bureaucratisation of informed consent”). My suggestions is that a critical notion of real autonomy and material wellbeing of the moral person (following Doyal- Sen-Van Parijs) should be applied to justify the distributive principles implied in any research on human beings, in particular in genomic research (benefit sharing.)

Published Online: 2009-02-13
Published in Print: 2009-February
Downloaded on 20.9.2025 from https://www.degruyterbrill.com/document/doi/10.1515/JIBL.2009.3/html
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