The Cambridge handbook of health research regulation
著者
書誌事項
The Cambridge handbook of health research regulation
Cambridge University Press, c2021
- : hardback
- タイトル別名
-
Handbook of health research regulation
Health research regulation
大学図書館所蔵 全3件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Other editors: Edward Dove, Agomoni Ganguli-Mitra, Catriona McMillan, Emily Postan, Nayha Sethi, Annie Sorbie
Includes bibliographical references and index
内容説明・目次
内容説明
The first ever interdisciplinary handbook in the field, this vital resource offers wide-ranging analysis of health research regulation. The chapters confront gaps between documented law and research in practice, and draw on legal, ethical and social theories about what counts as robust research regulation to make recommendations for future directions. The Handbook provides an account and analysis of current regulatory tools - such as consent to participation in research and the anonymization of data to protection participants' privacy - as well as commentary on the roles of the actors and stakeholders who are involved in human health research and its regulation. Drawing on a range of international examples of research using patient data, tissue and other human materials, the collective contribution of the volume is to explore current challenges in delivering good medical research for the public good and to provide insights on how to design better regulatory approaches. This title is also available as Open Access on Cambridge Core.
目次
- Introduction
- Part I. Concepts, Tools, Processes
- Section A. Concepts
- Introduction
- 1. Vulnerability
- 2. Autonomy
- 3. Proportionality
- 4. Social Value
- 5. Solidarity
- 6. Public Interest
- 7. Privacy
- 8. Trust and Institutions: Global Health Research Collaborations
- 9. Vulnerabilities and Power: The Political Side of Health Research
- Section B. Tools and Processes
- Introduction
- 10. Consent
- 11. Forms of Engagement
- 12. Participatory Governance in Health Research: Patients and Publics as Stewards of Health Research Systems
- 13. Risk-Benefit Analysis
- 14. The Regulatory Role of Patents in Innovative Health Research and Its Translation from the Laboratory to the Clinic
- 15. Benefit Sharing - From Compensation to Collaboration
- 16. Taking Failure Seriously: Health Research Regulation for Medical Devices, Technological Risk and Preventing Future Harm
- 17. Rules, Principles and the Added Value of Best Practice in Health Research Regulation
- 18. Research Ethics Review
- 19. Data Access Governance
- 20. Is the Red Queen Sitting on the Throne? Current Trends and Future Developments in Human Health Research Regulation
- 21. Regulatory Authorities and Decision-Making in Health Research: The Institutional Dimension
- 22. The Once and Future Role of Policy Advice for Health Regulation by Experts and Advisory Committees
- Part II: Reimagining Health Research Regulation
- Section A: Private and Public Dimensions of Health Research Regulation
- Introduction
- 23. Changing Identities in Disclosure of Research Findings
- 24. Health Research and Privacy through the Lens of Public Interest: A Monocle for the Myopic?
- 25. Mobilising Public Expertise in Health Research Regulation
- 26. Towards Adaptive Governance in Big Data Health Research: Implementing Regulatory Principles
- 27. Regulating Automated Healthcare and Research Technologies: First Do No Harm (to the Commons)
- Section B: Widening the Lens
- Introduction
- 28.When Learning is Continuous: Bridging the Research-Therapy Divide in the Regulatory Governance of Artificial Intelligence as Medical Devices
- 29. The Oversight of Clinical Innovation in a Medical Marketplace
- 30. The Challenge of 'Evidence': Research and Regulation of Traditional and Non-Conventional Medicines
- 31. Experiences of Ethics, Governance, and Scientific Practice in Neuroscience Research
- 32. Humanitarian Research: Ethical Considerations in Conducting Research during Global Health Emergencies
- 33. Governance Framework for Advanced Therapies in Argentina
- Section C: Towards Responsive Regulation
- Introduction
- 34. Human Gene Editing: Traversing Normative Systems
- 35. Towards a Global Germline Ethics? Human Heritable Genetic Modification and the Future of Health Research Regulation
- 36. Human Organs and Animal Bodies: Regulating Interspecies Research
- 37. When is Human? Rethinking the 14-day Rule
- 38. A Perfect Storm: Non-Evidence-Based Medicine in the Fertility Clinic
- 39. Margins or Mainstream? Enhancement and the Need for a New Regulatory Perspective
- Afterword: What Could a Learning Health Research Regulation System Look Like?
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