Informed Consent™: A Guide to the Risks and Benefits of Volunteering for Clinical Trials

Please note this publication is being discontinued: 40% off remaining stock

Informed Consent™ is a 300-page book designed to assist patients, their family and advocates in making more informed decisions before giving their consent to volunteer for a clinical trial and during their participation. This first-of-its-kind consumer guidebook provides comprehensive facts and objective, expert commentary to assist patients and their advocates in understanding their rights and recourse as study volunteers, what to expect when participating in a clinical trial and how research professionals conduct studies on new drug therapies.

Written by Ken Getz and Deborah Borfitz, the book has been reviewed extensively by regulatory and research professionals, patient advocates and consumers. Specific topics covered in the guide include:

  • Your rights as a volunteer, and how to protect them
  • A detailed review of the clinical trial process
  • How to determine if a clinical trial is right for you
  • How to find and evaluate clinical trials
  • Special considerations for vulnerable populations including children, prisoners and the elderly
  • What to do when things go wrong
  • A useful and practical appendix of reference information

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Customer Reviews:

"My personal experience in losing a son in a gene therapy trial exposed many very serious flaws in the informed consent process. This book informs the average human being about what to expect and ask when participating in clinical research. It is a book long overdue." Paul Gelsinger, From his 'Foreword' in Informed Consent?/i>

"…A comprehensive and balanced treatment of this important subject, providing the research participant with the information and tools to make an informed decision. A must read for research participants and professionals alike." Carol Saunders, Executive Director, New England Institutional Review Board

Media Reviews:

"If you’re wondering how medical research really works or whether or not you or a family member should participate in a clinical trial, this is the book for you. Under the auspices of the same publishing house that issues the reputable Physician’s Desk Reference (PDR), the authors have provided a comprehensive guide to the world of clinical trials from the prospective participant’s point of view." Quest magazine, 2002

"This book is designed to provide the necessary information for patients, their advocates and consumers to determine if they want to participate and then identify and carefully evaluate clinical trials. The book includes chapters on the clinical trial process and finding clinical trials, asking the right questions, and what participants can do when things go wrong." IRB Advisor, July 2002

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Perfect for:

  • Consumers and patients interested in identifying and participating in clinical trials
  • Clinical research and healthcare professionals interested in educating their patients about clinical trials

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Prices: International

   

Discounted Price: $11.99

 

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