Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities? After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries.
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This book explores the ethical and policy challenges of benefit sharing in relation to human biological resources. It presents possible ways forward to achieve justice in low- and middle-income countries, where biomedical research is increasingly carried out.
Les informations fournies dans la section « A propos du livre » peuvent faire référence à une autre édition de ce titre.
Vendeur : killarneybooks, Inagh, CLARE, Irlande
Hardcover. Etat : Very Good. Hardcover, xxvii + 234 pages, NOT ex-library. Printed in the Netherlands. Book is clean with unmarked text, free of inscriptions and stamps, firmly bound. Boards show gentle handling wear, a few scratches. Published without a dust jacket. -- Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities? After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries. -- Contents: 1 Benefit Sharing: From Biodiversity to Human Genetics: An Introduction; 2 Exploring Central Philosophical Concepts in Benefit Sharing: Vulnerability, Exploitation and Undue Inducement; 3 Legal Frameworks for Benefit Sharing: From Biodiversity to Human Genomics; 4 Sharing Traditional Knowledge: Who benefits? Cases from India, Nigeria, Mexico and South Africa; 5 Donating Human Samples: Who Benefits? Cases from Iceland, Kenya and Indonesia; 6 Fair for Women? A Gender Analysis of Benefit Sharing; 7 Promoting an Inclusive Approach to Benefit Sharing: Expanding the Scope of the CBD?; 8 Realizing Benefit Sharing: Is there a Role for Ethics Review?; 9 Beyond Benefit Sharing: Steps Towards Realizing the Human Right to Health; 10 Towards Best Practice for Benefit Sharing Involving Access to Human Biological Resources: Conclusions and Recommendations; Index. N° de réf. du vendeur 007856
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Vendeur : StainesBookhub, Weybridge, SURRE, Royaume-Uni
Etat : New. A brand new book in pristine condition. Showing zero signs of shelf wear, creases, or damage. N° de réf. du vendeur SPRLISTINGBYSHB16238
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Vendeur : Brook Bookstore On Demand, Napoli, NA, Italie
Etat : new. Questo è un articolo print on demand. N° de réf. du vendeur PVHPHOQ1CF
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Vendeur : BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Allemagne
Buch. Etat : Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries. 264 pp. Englisch. N° de réf. du vendeur 9789400762046
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Vendeur : Ria Christie Collections, Uxbridge, Royaume-Uni
Etat : New. In. N° de réf. du vendeur ria9789400762046_new
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Vendeur : moluna, Greven, Allemagne
Etat : New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. First comprehensive analysis of benefit sharing in relation to human biological resources The result of global collaboration between academics, policy advisors and policy makers from developed and developing countries Provides urgently need. N° de réf. du vendeur 5827615
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Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
Buch. Etat : Neu. Druck auf Anfrage Neuware - Printed after ordering - Biomedical research is increasingly carried out in low- and middle-income countries. International consensus has largely been achieved around the importance of valid consent and protecting research participants from harm. But what are the responsibilities of researchers and funders to share the benefits of their research with research participants and their communities After setting out the legal, ethical and conceptual frameworks for benefit sharing, this collection analyses seven historical cases to identify the ethical and policy challenges that arise in relation to benefit sharing. A series of recommendations address possible ways forward to achieve justice for research participants in low- and middle-income countries. N° de réf. du vendeur 9789400762046
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Vendeur : Books Puddle, New York, NY, Etats-Unis
Etat : New. pp. 264. N° de réf. du vendeur 2697184228
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Vendeur : Majestic Books, Hounslow, Royaume-Uni
Etat : New. Print on Demand pp. 264 Illus. N° de réf. du vendeur 96294459
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Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
Etat : New. PRINT ON DEMAND pp. 264. N° de réf. du vendeur 1897184238
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