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Xenotransplantation and Risk
Regulating a Developing Biotechnology

$99.00

Part of Cambridge Law, Medicine and Ethics

  • Date Published: December 2011
  • availability: In stock
  • format: Hardback
  • isbn: 9780521195768

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  • Some developing biotechnologies challenge accepted legal and ethical norms because of the risks they pose. Xenotransplantation (cross-species transplantation) may prolong life but may also harm the xeno-recipient and the public due to its potential to transmit infectious diseases. These trans-boundary diseases emphasise the global nature of advances in health care and highlight the difficulties of identifying, monitoring and regulating such risks and thereby protecting individual and public health. Xenotransplantation raises questions about how uncertainty and risk are understood and accepted, and exposes tensions between private benefit and public health. Where public health is at risk, a precautionary approach informed by the harm principle supports prioritising the latter, but the issues raised by genetically engineered solid organ xenotransplants have not, as yet, been sufficiently discussed. This must occur prior to their clinical introduction because of the necessary changes to accepted norms which are needed to appropriately safeguard individual and public health.

    • Explores whether xenotransplantation can be accommodated within existing legal and ethical norms and looks at the legal and ethical, practical implications of allowing clinical genetically engineered solid organ xenotransplants
    • Considers how risks are and can be regulated, particularly in situations of uncertainty and/or ignorance
    • International and comparative aspects of the analysis facilitate the learning of relevant lessons from selected jurisdictions
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    Product details

    • Date Published: December 2011
    • format: Hardback
    • isbn: 9780521195768
    • length: 306 pages
    • dimensions: 235 x 155 x 15 mm
    • weight: 0.6kg
    • availability: In stock
  • Table of Contents

    1. Introducing the issues
    2. Dealing with risk
    3. Regulating experimental procedures and medical research
    4. Regulatory responses to developing biotechnologies
    5. Challenges to legal and ethical norms: first party consent and third parties at risk
    6. Surveillance and monitoring: balancing public health and individual freedom
    7. Looking to the future.

  • Author

    Sara Fovargue, Lancaster University
    Sara Fovargue is a Senior Lecturer in Law at Lancaster University, where she specialises in health care law and ethics. Her main interests are clinical research involving human and non-human animals, risk and regulation with regards to developing biotechnologies and decision-making practices for vulnerable groups within health care law and practice.

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