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Human Subjects Research Regulation: Perspectives on the Future

✍ Scribed by I. Glenn Cohen and Holly Fernandez Lynch (eds.)


Publisher
MIT Press
Year
2014
Tongue
English
Leaves
392
Series
Basic Bioethics
Category
Library

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✦ Synopsis


Experts from different disciplines offer novel ideas for improving research oversight and protection of human subjects.

The current framework for the regulation of human subjects research emerged largely in reaction to the horrors of Nazi human experimentation, revealed at the Nuremburg trials, and the Tuskegee 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 remained fundamentally unchanged for decades. Yet, as this book documents, it has significant flawsβ€”including its potential to burden important research, overprotect some subjects and inadequately protect others, generate inconsistent results, and lag behind developments in how research is conducted. 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 this field from ethics, law, medicine, and public policy to discuss how to make the system better. The result is a collection of novel ideasβ€”some incremental, some radicalβ€”for the future of research oversight and human subject protection.

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

Contributors Adam Braddock, Alexander Morgan Capron, Ellen Wright Clayton, I. Glenn Cohen, Susan Cox, Amy L. Davis, Hilary Eckert, Barbara J. Evans, Nir Eyal, Heidi Li Feldman, Benjamin Fombonne, Elisa A. Hurley, Ana S. Iltis, Gail H. Javitt, Greg Koski, 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

✦ Table of Contents


Setting the stage : the past and present of human subjects research regulations / Amy L. Davis and Elisa A. Hurley --
De minimis risk : a suggestion for a new category of research risk / Rosamond Rhodes --
Risk level, research oversight, and decrements in participant protections / Ana S. Iltis --
Classifying military personnel as a vulnerable population / Efthimios Parasidis --
Children as research partners in community pediatrics / Adam Braddock --
Back to the future? : examining the Institute of Medicine's recommendations to loosen restrictions on using prisoners as human subjects / Osagie K. Obasogie --
Toward human research protection that is evidence based and participant centered / Michael McDonald, Susan Cox, and Anne Townsend --
Outsourcing ethical obligations : should the revised common rule address the responsibilities of investigators and sponsors? / Seema K. Shah --
Subjects, participants, and partners : what are the implications for research as the role of informed consent evolves? / Alexander Morgan Capron --
Democratic deliberation and the ethical review of human subjects research / Govind Persad --
IRBs and the problem of "local precedents" / Laura Stark --
Biospecimen exceptionalism in the ANPRM / Ellen Wright Clayton --
Biobanking, consent, and certificates of confidentiality : does the ANPRM muddy the water? / Brett A. Williams and Leslie E. Wolf --
Mandating consent for future research with biospecimens : a call for enhanced community engagement / Carol Weil, Hilary Shutak, Benjamin Fombonne, and Nicole Lockhart --
Take another little piece of my heart : regulating the research use of human biospecimens / Gail H. Javitt --
Reconsidering privacy protections for human research / Suzanne M. Rivera --
In search of sound policy on nonconsensual uses of identifiable health data / Barbara J. Evans --
What is this thing called research? / Zachary M. Schrag --
What's right about the "medical model" in human subjects research regulation / Heidi Li Feldman --
Three challenges for risk-based (research) regulation : heterogeneity among regulated activities, regulator bias, and stakeholder heterogeneity / Michelle N. Meyer --
Protecting human research subjects as human research workers / holly Fernandez Lynch --
Getting past protectionism : is it time to take off the training wheels? / Greg Koski --
Appendix. Regulatory changes in the ANPRM : comparison of existing rules with some of the changes being considered.


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