Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary

Ethical and Regulatory Aspects of Clinical Research: Readings and Commentary
ISBN-10
0801878136
ISBN-13
9780801878138
Category
Medical ethics
Pages
490
Language
English
Published
2003
Publisher
Johns Hopkins University Press
Author
Ezekiel J. Emanuel

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.

Similar books

  • Ethical Conduct of Clinical Research Involving Children
    By Institute of Medicine, Board on Health Sciences Policy, Committee on Clinical Research Involving Children

    The book looks at the need for appropriate pediatric expertise at all stages of the design, review, and conduct of a research project to effectively implement policies to protect children.

  • Ethical Issues in Clinical Research: A Practical Guide
    By Bernard Lo

    This book teaches researchers how to resolve the ethical dilemmas that can arise at any stage in clinical research.

  • Reviewing Clinical Trials: A Guide for the Ethics Committee
    By Washington, Inc, Chinese University of Hong Kong

    The idea for this manual came from Pfizer in the US, which provided the Clinical Trials Centre at The University of Hong Kong, Hong Kong SAR, PR China with a nonbinding grant for its development.

  • Principles and Practice of Clinical Research
    By John I. Gallin, Frederick P Ognibene

    The second edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research.

  • Ethics and Regulation of Clinical Research
    By Robert J. Levine

    In this book, Dr. Robert J. Levine reviews federal regulations, ethical analysis, and case studies in an attempt to answer these questions.

  • Ethics and the Pharmaceutical Industry
    By Michael A. Santoro, Thomas M. Gorrie

    The contributions in this book by leading figures in industry, government, NGOs, the medical community, and academia discuss and propose solutions to the ethical dilemmas of drug industry behavior.

  • Safety, Ethics and Regulations
    By Phuc Van Pham, Achim Rosemann

    Saftey, Ethics, and Regulations and the other books in the Stem Cells in Clinical Applications series will be invaluable to scientists, researchers, advanced students and clinicians working in stem cells, regenerative medicine or tissue ...

  • Clinical Trials in Latin America: Where Ethics and Business Clash
    By Nuria Homedes, Antonio Ugalde

    Their findings are presented in this volume, the first in-depth analysis of clinical trials in the region. ​

  • Ethical Issues in International Biomedical Research: A Casebook
    By Ezekiel J. Emanuel, Christine Grady, James V. Lavery

    No other volume has this scope. Students in bioethics, public and international health, and ethics will find this book particularly useful.

  • Sharing Clinical Trial Data: Maximizing Benefits, Minimizing Risk
    By Institute of Medicine, Board on Health Sciences Policy, Committee on Strategies for Responsible Sharing of Clinical Trial Data

    This book will be of interest to stakeholders across the spectrum of research-from funders, to researchers, to journals, to physicians, and ultimately, to patients.