Häftad, Engelska, 2019
502 kr
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Emily Jackson – författare
Visar alla böcker från författaren Emily Jackson. Handla med fri frakt och snabb leverans.
36 produkter
36 produkter
- Nyhet
Häftad, Engelska, 2026662 kr
Skickas inom 5-8 vardagar
Medical Law: Text, Cases, and Materials provides a comprehensive discussion of the law and its ethical context using extracts from a wide range of cases and materials to encourage thoughtful debate.Medical Law offers students a thorough and accessible exploration of this complex topic. Key case extracts provide the legal context and background; extracts from materials supply differing ethical perspectives and outline current debates; and the authors' insightful commentary guide readers to help them form their own understanding of medical law.Key features:· Extracts from a wide variety of academic materials ensure students acquire an overview of a range of different perspectives · Insightful author commentary and detailed analysis ensures that students gain a thorough understanding of the ethical context in which the law operates · Central Issues sections at the start of each chapter outline the key concepts covered, and further reading sections at the end provide guidance on further sources for research · Also available as an e-book with functionality, navigation features, and links that offer extra learning supportNew to this edition:· Discussion of NHS organizational reforms under the Health and Care Act 2022. · Coverage of significant new negligence cases, including Paul v Wolverhampton NHS Trust (secondary victims/psychiatric injury) and McCulloch v Forth Valley Health Board (informed consent).· A new section on Public Inquiries as a response to systemic healthcare failings.· Coverage of the changes to be implemented by the Mental Health Act 2025.· A new section in the confidentiality and data chapter on the tort of Misuse of Private Information.· A significantly revised chapter on emerging technologies, including coverage of organoids/embryo models, as well as new material on the implications of AI for healthcare.· Coverage of developments in relation to abortion, including decriminalization for women and new 'buffer zone' legislation.· An explanation of the implications of the Terminally Ill Adults (End of Life) Bill.Digital formats and resources The 7th edition is available for students and institutions to purchase in a variety of formats: the e-book and Law Trove offer a mobile experience and convenient functionality tools, navigation features and links that offer extra learning support.For more information about e-books, please visit www.oxfordtextbooks.co.uk/ebooks- Häftad, Engelska, 2020
194 kr
Skickas inom 3-6 vardagar
Find out what Lena does on her busy day!Follow Lena as she goes to school, plays with her friends, and spends time with her family. She learns important lessons about being responsible, honest, and respectful. - Häftad, Engelska, 2002
898 kr
Skickas inom 7-10 vardagar
This book provides an accessible introduction to jurisprudence and legal theory. It sets out a course of study that offers a highly effective series of introductions into a wide variety of theories and theoretical perspectives, from traditional approaches such as Natural Law to modern ones such as Feminist Theory, Economic Analysis of Law and Foucault and Law, _ The book is designed for students of jurisprudence and legal theory, but it will also assist those studying law and legal systems within courses on Political Science, Philosophy and Sociology. - Inbunden, Engelska, 2022
402 kr
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- Häftad, Engelska, 2022
273 kr
Skickas inom 5-8 vardagar
- Inbunden, Engelska, 2022
388 kr
Skickas inom 5-8 vardagar
- Häftad, Engelska, 2022
244 kr
Skickas inom 5-8 vardagar
- Inbunden, Engelska, 2022
441 kr
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- Häftad, Engelska, 2022
316 kr
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- Häftad, Engelska, 2025
214 kr
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- Inbunden, Engelska, 2025
370 kr
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- Häftad, Engelska, 2024
596 kr
Skickas inom 10-15 vardagar
This assessment of Britain’s influential 14 day rule governing embryo research explores how and why it became the de facto global standard for research into human fertilisation and embryology, arguing that its influence and stability offers valuable lessons for successful biological translation.One of the most important features of the 14 day rule, the authors claim, is its reliance on sociological as well as ethical, legislative, regulatory and scientific principles. The careful integration of social expectations and perceptions, as well as sociological definitions of the law and morality, into the development of a robust legislative infrastructure of ‘human fertilisation and embryology’, enabled what has come to be known as the Warnock Consensus – a solid and enduring public acceptance that has enabled successive parliamentary approval for controversial areas of scientific research in the UK, such as stem cell research and mitochondrial donation, for over 30 years. These important sociological insights are increasingly relevant to new biotranslational challenges such as human germline gene editing and the use of AI assisted technologies in human reproduction. As the legislation around the 14 day rule begins to be reviewed worldwide, the important lessons we can learn from its global and enduring significance will apply not only to future legislation governing embryo research, but to the future of biological translation more widely.An important volume for those interested in reproductive studies, biogovernance and biological translation, it is suitable for researchers, clinicians and students in medicine, biosciences, sociology, and science and technology studies. - Inbunden, Engelska, 2024
2 539 kr
Skickas inom 10-15 vardagar
This assessment of Britain’s influential 14 day rule governing embryo research explores how and why it became the de facto global standard for research into human fertilisation and embryology, arguing that its influence and stability offers valuable lessons for successful biological translation.One of the most important features of the 14 day rule, the authors claim, is its reliance on sociological as well as ethical, legislative, regulatory and scientific principles. The careful integration of social expectations and perceptions, as well as sociological definitions of the law and morality, into the development of a robust legislative infrastructure of ‘human fertilisation and embryology’, enabled what has come to be known as the Warnock Consensus – a solid and enduring public acceptance that has enabled successive parliamentary approval for controversial areas of scientific research in the UK, such as stem cell research and mitochondrial donation, for over 30 years. These important sociological insights are increasingly relevant to new biotranslational challenges such as human germline gene editing and the use of AI assisted technologies in human reproduction. As the legislation around the 14 day rule begins to be reviewed worldwide, the important lessons we can learn from its global and enduring significance will apply not only to future legislation governing embryo research, but to the future of biological translation more widely.An important volume for those interested in reproductive studies, biogovernance and biological translation, it is suitable for researchers, clinicians and students in medicine, biosciences, sociology, and science and technology studies. - E-bokPDF, Engelska, 2024
628 kr
Läs direkt efter köp
This assessment of Britain’s influential 14 day rule governing embryo research explores how and why it became the de facto global standard for research into human fertilisation and embryology, arguing that its influence and stability offers valuable lessons for successful biological translation.
One of the most important features of the 14 day rule, the authors claim, is its reliance on sociological as well as ethical, legislative, regulatory and scientific principles. The careful integration of social expectations and perceptions, as well as sociological definitions of the law and morality, into the development of a robust legislative infrastructure of ‘human fertilisation and embryology’, enabled what has come to be known as the Warnock Consensus – a solid and enduring public acceptance that has enabled successive parliamentary approval for controversial areas of scientific research in the UK, such as stem cell research and mitochondrial donation, for over 30 years. These important sociological insights are increasingly relevant to new biotranslational challenges such as human germline gene editing and the use of AI assisted technologies in human reproduction. As the legislation around the 14 day rule begins to be reviewed worldwide, the important lessons we can learn from its global and enduring significance will apply not only to future legislation governing embryo research, but to the future of biological translation more widely.
An important volume for those interested in reproductive studies, biogovernance and biological translation, it is suitable for researchers, clinicians and students in medicine, biosciences, sociology, and science and technology studies.
- E-bokEngelska, 2024
628 kr
Läs direkt efter köp
This assessment of Britain’s influential 14 day rule governing embryo research explores how and why it became the de facto global standard for research into human fertilisation and embryology, arguing that its influence and stability offers valuable lessons for successful biological translation.
One of the most important features of the 14 day rule, the authors claim, is its reliance on sociological as well as ethical, legislative, regulatory and scientific principles. The careful integration of social expectations and perceptions, as well as sociological definitions of the law and morality, into the development of a robust legislative infrastructure of ‘human fertilisation and embryology’, enabled what has come to be known as the Warnock Consensus – a solid and enduring public acceptance that has enabled successive parliamentary approval for controversial areas of scientific research in the UK, such as stem cell research and mitochondrial donation, for over 30 years. These important sociological insights are increasingly relevant to new biotranslational challenges such as human germline gene editing and the use of AI assisted technologies in human reproduction. As the legislation around the 14 day rule begins to be reviewed worldwide, the important lessons we can learn from its global and enduring significance will apply not only to future legislation governing embryo research, but to the future of biological translation more widely.
An important volume for those interested in reproductive studies, biogovernance and biological translation, it is suitable for researchers, clinicians and students in medicine, biosciences, sociology, and science and technology studies.
162 kr
Skickas inom 3-6 vardagar
- Inbunden, Engelska, 2023
1 791 kr
Skickas inom 3-6 vardagar
- Inbunden, Engelska, 2020
224 kr
Skickas inom 5-8 vardagar
- Häftad, Engelska, 2020
151 kr
Skickas inom 5-8 vardagar
- Häftad, Engelska, 2020
151 kr
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- Häftad, Engelska, 2021
137 kr
Skickas inom 5-8 vardagar
- Häftad, Engelska, 2023
245 kr
Skickas inom 5-8 vardagar
- Inbunden, Engelska, 2001
840 kr
Skickas inom 10-15 vardagar
This new book provides a clear and accessible analysis of the various ways in which human reproduction is regulated. A comprehensive exposition of the law relating to birth control,abortion, pregnancy, childbirth, surrogacy and assisted conception is accompanied by an exploration of some of the complex ethical dilemmas that emerge when one of the most intimate areas of human life is subjected to regulatory control. Throughout the book, two principal themes recur. First, particular emphasis is placed upon the special difficulties that arise in regulating new technological intervention in all aspects of the reproductive process. Second, the concept of reproductive autonomy is both interrogated and defended. This book offers a readable and engaging account of the complex relationships between law, technology and reproduction. It will be useful for lecturers and students taking medical law or ethics courses. It should also be of interest to anyone with a more general interest in women's bodies and the law, or with the profound regulatory consequences of new technologies. - Häftad, Engelska, 2009
1 032 kr
Skickas inom 10-15 vardagar
These essays explore the nature and limits of individual autonomy in law, policy and the work of regulatory agencies. Authors ask searching questions about the nature and scope of the regulation of 'private' lives, from intimacies, personal relationships and domestic lives to reproduction. They question the extent to which the law does, or should, protect individual autonomy. Recent rapid advances in the development of new technologies - particularly those concerned with human genetics and assisted reproduction - have generated new questions (practical, social, legal and ethical) about how far the state should intervene in individual decision making. Is there an inevitable tension between individual liberty and the common good? How might a workable balance between the public and the private be struck? How, indeed, should we think about 'autonomy'? The essays explore the arguments used to create and maintain the boundaries of autonomy - for example, the protection of the vulnerable, public goods of various kinds, and the maintenance of tradition and respect for cultural practices. Contributors address how those boundaries should be drawn and interventions justified.How are contemporary ethical debates about autonomy constructed, and what principles do they embody? What happens when those principles become manifest in law? - E-bokPDF, Engelska, 2001
912 kr
Läs direkt efter köp
This new book provides a clear and accessible analysis of the various ways in which human reproduction is regulated. A comprehensive exposition of the law relating to birth control,abortion, pregnancy, childbirth, surrogacy and assisted conception is accompanied by an exploration of some of the complex ethical dilemmas that emerge when one of the most intimate areas of human life is subjected to regulatory control. Throughout the book, two principal themes recur. First, particular emphasis is placed upon the special difficulties that arise in regulating new technological intervention in all aspects of the reproductive process. Second, the concept of reproductive autonomy is both interrogated and defended. This book offers a readable and engaging account of the complex relationships between law, technology and reproduction. It will be useful for lecturers and students taking medical law or ethics courses. It should also be of interest to anyone with a more general interest in women''s bodies and the law, or with the profound regulatory consequences of new technologies. - E-bokPDF, Engelska, 2009
1 123 kr
Läs direkt efter köp
These essays explore the nature and limits of individual autonomy in law, policy and the work of regulatory agencies. Authors ask searching questions about the nature and scope of the regulation of ''private'' lives, from intimacies, personal relationships and domestic lives to reproduction. They question the extent to which the law does, or should, protect individual autonomy. Recent rapid advances in the development of new technologies - particularly those concerned with human genetics and assisted reproduction - have generated new questions (practical, social, legal and ethical) about how far the state should intervene in individual decision making. Is there an inevitable tension between individual liberty and the common good? How might a workable balance between the public and the private be struck? How, indeed, should we think about ''autonomy''?The essays explore the arguments used to create and maintain the boundaries of autonomy - for example, the protection of the vulnerable, public goods of various kinds, and the maintenance of tradition and respect for cultural practices. Contributors address how those boundaries should be drawn and interventions justified. How are contemporary ethical debates about autonomy constructed, and what principles do they embody? What happens when those principles become manifest in law? - E-bokEngelska, 2011
393 kr
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In this new addition to the ''Debating Law'' series, Emily Jackson and John Keown re-examine the legal and ethical aspects of the euthanasia debate.Emily Jackson argues that we owe it to everyone in society to do all that we can to ensure that they experience a ''good death''. For a small minority of patients who experience intolerable and unrelievable suffering, this may mean helping them to have an assisted death. In a liberal society, where people''s moral views differ, we should not force individuals to experience deaths they find intolerable. This is not an argument in favour of dying. On the contrary, Jackson argues that legalisation could extend and enhance the lives of people whose present fear of the dying process causes them overwhelming distress. John Keown argues that voluntary euthanasia and physician-assisted suicide are gravely unethical and he defends their continued prohibition by law. He analyses the main arguments for relaxation of the law - including those which invoke the experience of jurisdictions which permit these practices - and finds them wanting. Relaxing the law would, he concludes, be both wrong in principle and dangerous in practice, not least for the dying, the disabled and the disadvantaged. - E-bokPDF, Engelska, 2012
631 kr
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The principal purpose of this book is to tell the story of a medicine''s journey through the regulatory system in the UK, from defining what counts as a medicine, through clinical trials, licensing, pharmacovigilance, marketing and funding. The question of global access to medicines is addressed because of its political importance, and because it offers a particularly stark illustration of the consequences of classifying medicines as a private rather than a public good.Two further specific challenges to the future of medicine''s regulation are examined separately: first, pharmacogenetics, or the genetic targeting of medicines to subgroups of patients, and second, the possibility of using medicines to enhance well-being or performance, rather than treat disease.Throughout, the emphasis is on the role of regulation in shaping and influencing the operation of the medicines industry, an issue that is of central importance to the promotion of public health and the fair and equitable distribution of healthcare resources. - E-bokEngelska, 2012
631 kr
Läs direkt efter köp
The principal purpose of this book is to tell the story of a medicine''s journey through the regulatory system in the UK, from defining what counts as a medicine, through clinical trials, licensing, pharmacovigilance, marketing and funding. The question of global access to medicines is addressed because of its political importance, and because it offers a particularly stark illustration of the consequences of classifying medicines as a private rather than a public good.Two further specific challenges to the future of medicine''s regulation are examined separately: first, pharmacogenetics, or the genetic targeting of medicines to subgroups of patients, and second, the possibility of using medicines to enhance well-being or performance, rather than treat disease.Throughout, the emphasis is on the role of regulation in shaping and influencing the operation of the medicines industry, an issue that is of central importance to the promotion of public health and the fair and equitable distribution of healthcare resources.
