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El. knyga: Human Subjects Research Regulation: Perspectives on the Future

Edited by (Harvard Law School), Edited by (Harvard Law School)
  • Formatas: 392 pages
  • Serija: Basic Bioethics
  • Išleidimo metai: 25-Jul-2014
  • Leidėjas: MIT Press
  • Kalba: eng
  • ISBN-13: 9780262320825
  • Formatas: 392 pages
  • Serija: Basic Bioethics
  • Išleidimo metai: 25-Jul-2014
  • Leidėjas: MIT Press
  • Kalba: eng
  • ISBN-13: 9780262320825

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The current framework for the regulation of human subjects research emerged largelyin reaction to the horrors of Nazi human experimentation, revealed at the Nuremburg trials, and theTuskegee syphilis study, conducted by U.S. government researchers from 1932 to 1972. This framework,combining elements of paternalism with efforts to preserve individual autonomy, has remainedfundamentally unchanged for decades. Yet, as this book documents, it has significant flaws --including its potential to burden important research, overprotect some subjects and inadequatelyprotect others, generate inconsistent results, and lag behind developments in how research isconducted. Invigorated by the U.S. government's first steps toward change in over twenty years, Human Subjects Research Regulation brings together the leading thinkers in thisfield from ethics, law, medicine, and public policy to discuss how to make the system better. Theresult is a collection of novel ideas -- some incremental, some radical -- for the future ofresearch oversight and human subject protection.

After reviewing the history ofU.S. research regulations, the contributors consider such topics as risk-based regulation; researchinvolving vulnerable populations (including military personnel, children, and prisoners); therelationships among subjects, investigators, sponsors, and institutional review boards; privacy,especially regarding biospecimens and tissue banking; and the possibility of fundamental paradigmshifts.

ContributorsAdam Braddock, Alexander Morgan Capron,Ellen Wright Clayton, I. Glenn Cohen, Susan Cox, Amy L. Davis, Hilary Eckert, Barbara J. Evans, NirEyal, Heidi Li Feldman, Benjamin Fombonne, Elisa A. Hurley, Ana S. Iltis, Gail H. Javitt, GregKoski, Nicole Lockhart, Holly Fernandez Lynch, Michael McDonald, Michelle N. Meyer, Osagie K.Obasogie, Efthimios Parasidis, Govind Persad, Rosamond Rhodes, Suzanne M. Rivera, Zachary M. Schrag,Seema K. Shah, Jeffrey Skopek, Laura Stark, Patrick Taylor, Anne Townsend, Carol Weil, Brett A.Williams, Leslie E. Wolf

Series Foreword xi
Acknowledgments xiii
Introduction 1(8)
I. Glenn Cohen
Holly Fernandez Lynch
1 Setting the Stage: The Past and Present of Human Subjects Research Regulations
9(18)
Amy L. Davis
Elisa A. Hurley
I Regulation of Risk
Introduction
27(4)
Nir Eyal
2 De minimis Risk: A Suggestion for a New Category of Research Risk
31(14)
Rosamond Rhodes
3 Risk Level, Research Oversight, and Decrements in Participant Protections
45(16)
Ana S. Iltis
II Protection of Vulnerable Populations
Introduction
61(4)
Patrick Taylor
4 Classifying Military Personnel as a Vulnerable Population
65(14)
Efthimios Parasidis
5 Children as Research Partners in Community Pediatrics
79(14)
Adam Braddock
6 Back to the Future? Examining the Institute of Medicine's Recommendations to Loosen Restrictions on Using Prisoners as Human Subjects
93(16)
Osagie K. Obasogie
III Redefining the Participant--Researcher Relationship and the Role of IRBs
Introduction
109(4)
I. Glenn Cohen
7 Toward Human Research Protection That Is Evidence Based and Participant Centered
113(14)
Michael McDonald
Susan Cox
Anne Townsend
8 Outsourcing Ethical Obligations: Should the Revised Common Rule Address the Responsibilities of Investigators and Sponsors?
127(16)
Seema K. Shah
9 Subjects, Participants, and Partners: What Are the Implications for Research as the Role of Informed Consent Evolves?
143(14)
Alexander Morgan Capron
10 Democratic Deliberation and the Ethical Review of Human Subjects Research
157(16)
Govind Persad
11 IRBs and the Problem of "Local Precedents"
173(16)
Laura Stark
IV Specimens, Data, and Privacy
Introduction
189(4)
Jeffrey Skopek
12 Biospecimen Exceptionalism in the ANPRM
193(14)
Ellen Wright Clayton
13 Biobanking, Consent, and Certificates of Confidentiality: Does the ANPRM Muddy the Water?
207(14)
Brett A. Williams
Leslie E. Wolf
14 Mandating Consent for Future Research with Biospecimens: A Call for Enhanced Community Engagement
221(16)
Carol Weil
Hilary Shutak
Benjamin Fombonne
Nicole Lockhart
15 Take Another Little Piece of My Heart: Regulating the Research Use of Human Biospecimens
237(14)
Gail H. Javitt
16 Reconsidering Privacy Protections for Human Research
251(14)
Suzanne M. Rivera
17 In Search of Sound Policy on Nonconsensual Uses of Identifiable Health Data
265(16)
Barbara J. Evans
V Paradigm Shifts in Research Ethics
Introduction
281(4)
I. Glenn Cohen
18 What Is This Thing Called Research?
285(14)
Zachary M. Schrag
19 What's Right about the "Medical Model" in Human Subjects Research Regulation
299(14)
Heidi Li Feldman
20 Three Challenges for Risk-Based (Research) Regulation: Heterogeneity among Regulated Activities, Regulator Bias, and Stakeholder Heterogeneity
313(14)
Michelle N. Meyer
21 Protecting Human Research Subjects as Human Research Workers
327(14)
Holly Fernandez Lynch
22 Getting Past Protectionism: Is It Time to Take off the Training Wheels?
341(8)
Greg Koski
Appendix: Regulatory Changes in the ANPRM: Comparison of Existing Rules with Some of the Changes Being Considered 349(10)
Contributors 359(4)
Index 363