Product Description

All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. Based on a course taught by the editors at NIH, Ethical and Regulatory Aspects of Clinical Research is the first book designed to help investigators meet this new requirement. The book begins with the history of human subjects research and guidelines instituted since World War II. It then covers various stages and components of the clinical trial process: designing the trial, recruiting participants, ensuring informed consent, studying special populations, and conducting international research. Concluding chapters address conflicts of interest, scientific misconduct, and challenges to the IRB system. The appendix provides sample informed consent forms.

This book will be used in undergraduate courses on research ethics and in schools of medicine and public health by students who are or will be carrying out clinical research. Professionals in need of such training and bioethicists also will be interested.

Product Details

• Amazon Sales Rank: #441137 in Books
• Published on: 2003-09-30
• Number of items: 1
• Binding: Paperback
• 528 pages

Review

"Provides excellent material on a broad variety of ethical topics in clinical research. The editors are commended for the wise and diverse selection of articles and the broad range of sources of literature included. A lot of information is made available at a very affordable price." -- Quality Assurance Journal

"Many of the chapters easily deserve to be required reading... Most of the readings that have been chosen for the book can lay claim to being classics. They represent sophisticated thinking on various topics." -- Leonardo D. de Castro, Bulletin of the World Health Organization

"One word will suffice to describe the book -- outstanding." -- Sanjay A. Pai, Current Science

About the Author

Ezekiel J. Emanuel, M.D., Ph.D., is Chair of the Department of Clinical Bioethics at the Warren G. Magnuson Clinical Center at the National Institutes of Health. Robert A. Crouch, M.A., is an Assistant Professor in the Biomedical Ethics Unit and the Department of Social Studies of Medicine at McGill University. John D. Arras, Ph.D., is Porterfield Professor of Biomedical Ethics and Professor of Philosophy at the University of Virginia. Jonathan D. Moreno, Ph.D., is Director of the Center for Biomedical Ethics at the University of Virginia. Christine Grady, R.N., Ph.D., is Head, Section on Human Subjects Research in the Department of Clinical Bioethics at the National Institutes of Health.

Customer Reviews

Excellent Reference
This book is a great resource and reference. It's a great collection of short articles useful for those interested in the ethical issues surrounding research. It has full copies of the Nuremberg and other ethical codes.

Very informative
This book is an excellent textbook for bioethics with wonderful framework, comprehensive approach, and many relevant articles.
You can get overall outline and detailed information & discussion on bioethics by this book, therefore this book is good for beginner as well as for expert on this field.