Population genomics research drawing on genetic databases has expanded rapidly, with some of this information being combined in 'biobanks'. Managing this information in an appropriate way is a highly complex ethical issue in the health policy arena. This book combines theoretical and empirical research to analyze the areas of conflict and consensus in the regulatory and ethical frameworks that have been developed to govern biobanks.
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Bernice Elger is Professor, Institut Universitaire Romand de Medecine Legale Universite de Geneve, and Internist at the University Hospital of Geneva. Nikola Biller-Andorno is Professor of Biomedical Ethics, University of Zurich. She is an advisor to the World Health Organization and Associate Editor of the Journal of Medical Ethics. Alex Mauron is Professor of Bioethics, Faculty of Medicine, University of Geneva. He is a member of the Swiss Academy of Medical Sciences, the Swiss National Advisory Commission on Biomedical Ethics, and the Swiss Science and Technology Council. Alex Capron is a University Professor at the University of Southern California, where he holds the Scott H. Bice Chair in Healthcare Law, Policy and Ethics. A member of the Institute of Medicine (National Academy of Sciences) and the American Law Institute, he was the first Director of Ethics, Trade, Human Rights and Health Law at the World Health Organization.
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Buch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Population genomics research drawing on genetic databases has expanded rapidly, with some of this information being combined in 'biobanks'. Managing this information in an appropriate way is a highly complex ethical issue in the health policy arena. This book combines theoretical and empirical research to analyze the areas of conflict and consensus in the regulatory and ethical frameworks that have been developed to govern biobanks. Ethicists from the Department of Ethics, Trade, Human Rights and Health Law (ETH) of the World Health Organization, the Institute of Biomedical Ethics of Geneva University and the Institute of Biomedical Ethics of the University of Zurich, with the support of the Geneva International Academic Network (GIAN), examine the conditions under which genetic databases can be established, kept, and made use of in an ethically acceptable way. In addition to a comprehensive review of the scientific literature and a comparative analysis of existing normative frameworks, they present the results of in-depth interviews with experts around the world concerning the most unresolved and controversial issues. The results of that study, combined with their normative analysis, leads to recommendations for a better international framework. 270 pp. Englisch. N° de réf. du vendeur 9780754672555
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Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Bernice Elger is Professor, Institut Universitaire Romand de Medecine Legale Universite de Geneve, and Internist at the University Hospital of Geneva. Nikola Biller-Andorno is Professor of Biomedical Ethics, University of Zurich. She is an advisor to the . N° de réf. du vendeur 594955344
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