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Bemærk: Kan ikke leveres før jul.
This book presents an investigation into the need for an EU-level framework to regulate genetic information. It is ideal for legal and... Læs mere
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This book provides the tools for understanding the concerns, fears and biases people with disabilities and bioethicists have that the health care setting is a dangerous place and that disability activists have nothing to offer bioethics.
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Alasdair Maclean examines the ethical basis for consent to medical treatment, arguing that consent should be approached in the context of... Læs mere
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This volume maps the areas of ethical concern in the debate regarding the governance of genetic information, and suggests alternative ethical frameworks and models of regulation in order to inform its restructuring.
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This book is for legal, development, policy and health scholars who are interested in global health law.... Læs mere
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Written for academics and policymakers working in health and social care, this timely book takes the debate on healthcare access beyond the usual... Læs mere
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Human genetic databases raise many ethical, legal and social questions. In this book, first published in 2007, bioethics... Læs mere
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This book provides an overview of developments in personalized medicine patenting, which develops medical treatments tailored to... Læs mere
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This book explores science, psychology and the law. Drawing on sources from science fiction films to the Congressional Record, it unmasks the... Læs mere
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Offers approaches to social and political issues that have become polarized and resistant to compromise. The cross-disciplined authorship... Læs mere
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New technologies and increased data sharing have a great potential to advance health research, but our current safeguards for privacy, confidentiality and... Læs mere
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Written for academics, policymakers, and the public, this important work explains how our justice system handles widespread harms over... Læs mere