Website Index


Home

Directory of 1,000 Healthcare Recruiters  physician recruiters

Health Administration Toolbox 

Calendar of Health Observance Dates

Recommended Reading Lists & Healthcare Bookstore New!

Job Search Resources  

Career & Interview Resources 

Glossary of Managed Care Terms 

Health Care Companies & Hospitals 

Health & Medical Associations 

Tools for Physician Executives 

Tools for Finance Directors 

Tools for Nursing Managers 

Tools for Personnel Managers 

Tools for Traveling Executives 

Search this Site


About Us

About Pam Pohly Associates

Info for Healthcare Employers 

Info for Job Hunters

Jobs to Apply for  

Our Hot Jobs 

Pam Pohly's Background

Contact Us





 

 

To search this site, click here

Copyright©, Pam Pohly, All Rights Reserved.  

Return Home

 



You are here > Home > Reading Lists > Compliance Resources > Ethical & Regulatory Aspects of Clinical Research

Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
edited by Ezekiel J. Emanuel, M.D., Ph.D., Robert A. Crouch, M.A., John D. Arras, Ph.D., Jonathan D. Moreno, Ph.D., and Christine Grady, R.N., Ph.D. 

Softcover, 528 pp
ISBN 0801878136
Johns Hopkins University Press
January 2004
(click below for the very best currently available price for this important resource)

All investigators funded by the National Institutes of Health are now required to receive training about the ethics of clinical research. 

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 is read by:

  • Professionals and investigators in need of training to meet NIH standards
  • Bioethicists in all medical settings
  • Professionals carrying out clinical research, and,
  • Students in research and medical ethics courses

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.

(information from the publisher)

You may also be interested in / The Directory of Healthcare Recruiters /

Jump to a List / Health Administration & Leadership / Physician Executive, Medical Staff & Practice Management / Finance, Accounting, Economics, Billing & Reimbursement / Coding for Hospital, Physician & Clinical Services / Law, Malpractice, Ethics, Accreditation & Compliance / Quality Improvement, Outcomes & Customer Service / Risk Management, Security, Error Reduction & Patient Safety / Information Systems, Technology & Medical Records / Clinical Management & Executive Nursing / Behavioral Health, Social Work & Psychiatry Management / Human Resources, Management & Supervision / Directories, Data, Trends & Benchmarks / Software & CD-ROMs / Gift Ideas & Recommended Gifts / Journals, Magazines & Newsletters / Search for Books / Books Index /

Go Back to Pages / Home Page / Toolbox for Health Administrators / Bookstore