
- English
- PDF
- Available on iOS & Android
Rethinking Informed Consent in Bioethics
About this book
Informed consent is a central topic in contemporary biomedical ethics. Yet attempts to set defensible and feasible standards for consenting have led to persistent difficulties. In Rethinking Informed Consent in Bioethics, first published in 2007, Neil Manson and Onora O'Neill set debates about informed consent in medicine and research in a fresh light. They show why informed consent cannot be fully specific or fully explicit, and why more specific consent is not always ethically better. They argue that consent needs distinctive communicative transactions, by which other obligations, prohibitions, and rights can be waived or set aside in controlled and specific ways. Their book offers a coherent, wide-ranging and practical account of the role of consent in biomedicine which will be valuable to readers working in a range of areas in bioethics, medicine and law.
Frequently asked questions
- Essential is ideal for learners and professionals who enjoy exploring a wide range of subjects. Access the Essential Library with 800,000+ trusted titles and best-sellers across business, personal growth, and the humanities. Includes unlimited reading time and Standard Read Aloud voice.
- Complete: Perfect for advanced learners and researchers needing full, unrestricted access. Unlock 1.4M+ books across hundreds of subjects, including academic and specialized titles. The Complete Plan also includes advanced features like Premium Read Aloud and Research Assistant.
Please note we cannot support devices running on iOS 13 and Android 7 or earlier. Learn more about using the app.
Information
Table of contents
- Cover
- Half-title
- Title
- Copyright
- Contents
- Preface
- Acknowledgements
- CHAPTER 1 Consent: Nuremberg, Helsinki and beyond
- CHAPTER 2 Information and communication: the drift from agency
- CHAPTER 3 Informing and communicating: back to agency
- CHAPTER 4 How to rethink informed consent
- CHAPTER 5 Informational privacy and data protection
- CHAPTER 6 Genetic information and genetic exceptionalism
- CHAPTER 7 Trust, accountability and transparency
- Some conclusions and proposals
- Bibliography
- Institutional sources and documents
- Index