Law and Ethics in Biomedical Research : : Regulation, Conflict of Interest and Liability / / ed. by Trudo Lemmens, Duff Waring.
When a young man named Jesse Gelsinger died in 1999 as a result of his participation in a gene transfer research study, regulatory agencies in the United States began to take a closer look at what was happening in medical research. The resulting temporary shutdown of some of the most prestigious aca...
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Superior document: | Title is part of eBook package: De Gruyter University of Toronto Press eBook-Package Backlist 2000-2013 |
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MitwirkendeR: | |
HerausgeberIn: | |
Place / Publishing House: | Toronto : : University of Toronto Press, , [2017] ©2006 |
Year of Publication: | 2017 |
Language: | English |
Online Access: | |
Physical Description: | 1 online resource (384 p.) |
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Table of Contents:
- Frontmatter
- Contents
- Acknowledgments
- Introduction
- 1. Uninformed Consent: The Case of Jesse Gelsinger
- Part One: Regulation
- 2. Questions and Challenges in the Governance of Research Involving Humans: A Canadian Perspective
- 3. Swinging on the Pendulum: Shifting Views of Justice in Human Subjects Research
- Part Two: Conflict of Interest
- 4. The Ethical and Legal Foundations of Scientific 'Conflict of Interest'
- 5. Self-Censorship
- 6. Promoting Integrity in Industry- Sponsored Clinical Drug Trials: Conflict of Interest Issues for Canadian Health Sciences Centres
- 7. The Human Subjects Trade: Ethical, Legal, and Regulatory Remedies to Deal with Recruitment Incentives and to Protect Scientific Integrity
- Part Three: Liability
- 8. Bringing Research into Therapy: Liability Anyone?
- 9. Legal Liability for Harm to Research Participants: The Case of Placebo-Controlled Trials
- 10. Her Majesty's Research Subjects: Liability of the Crown in Research Involving Humans
- Contributors
- Index