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Full Product Details

Author:   Linda F. Hogle
Publisher:   Springer-Verlag New York Inc.
Imprint:   Springer-Verlag New York Inc.
Edition:   Softcover reprint of the original 1st ed. 2014
Dimensions:   Width: 15.50cm , Height: 1.30cm , Length: 23.50cm
Weight:   3.635kg
ISBN:  

9781493943456

ISBN 10:   1493943456
Pages:   227
Publication Date:   23 August 2016
Audience:   Professional and scholarly ,  Professional & Vocational
Format:   Paperback
Publisher's Status:   Active
Availability:   Manufactured on demand  
We will order this item for you from a manufactured on demand supplier.

Table of Contents

Part I: Foresight, hindsight and peripheral vision: Navigating contemporary legal, ethical and Policy issues in Regenerative Medicine.- Contemporary dilemmas facing regenerative medicine researchers: an overview.- Characterizing International Stem Cell Research Niches.- Policies and practices to enhance multi-sectorial collaborations and commercialization of regenerative medicine.- The Patenting Landscape for Human Embryonic Stem Cells.- Repositories for Sharing Human Data in Stem Cell Research.- PART II: Research Integrity: Updates for Regenerative Medicine Researchers.- Beyond the Checkboxes: Research Integrity for Regenerative Medicine Researchers.- Protecting Human Participants in the Procurement of Materials in Regenerative Medicine Research.- Early-Stage Research: Issues in Design and Ethics.

Reviews

From the book reviews: The book will appeal to ethicists and college professors who are interested in research ethics and/or ethical, legal, and social implications (ELSI) projects. The book also will be useful to a variety of students interested in law and bioethics, or who are planning to conduct RMR. ... this book provides many interesting insights into RMR, and those in the intended audience likely will find it to be useful, relevant, and thought provoking. (Joseph T. Norris, Doody's Book Reviews, September, 2014)

Author Information

Linda F. Hogle is Professor of Medical Social Sciences in the School of Medicine & Public Health at the University of Wisconsin-Madison and Fellow at the Wisconsin Institutes for Discovery.  Her research includes analyses of social, ethical, and legal issues in emerging cell-based and biomedical engineering technologies, as well as concepts of risk in innovative science as understood by governance bodies. She has served as an advisor to several international research consortia focusing on stem cell and regenerative medicine. Contributors include: Sean P. Palecek, University of Wisconsin-Madison, Department of Chemical and Biological Engineering, WI David Schaffer, University of California-Berkeley, Department of Chemical and Biomolecular Engineering, CA Peter W. Zandstra, University of Toronto, Institute of Biomaterials and Biomedical Engineering, ON, Canada David B. Resnik, National Institute of Environmental Health Sciences, NC Tania Bubela, University of Alberta, Department of Public Health Sciences, AB, Canada Amrita Mishra, University of Alberta, Department of Public Health Sciences, AB, Canada Debra J. H. Mathews, The Johns Hopkins University, Berman Institute of Bioethics, MD Kevin E. Noonan, McDonnell Boehnen Hulbert & Berghoff LLP, IL Pilar N. Ossorio, University of Wisconsin-Madison Law School, WI Jessica von Reyn, University of Wisconsin-Madison Law School, WI Nancy M. P. King, Wake Forest University School of Medicine, Department of Social Sciences and Health Policy, NC Amritava Das, University of Wisconsin-Madison, Department of Chemical and Biological Engineering, WI

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