Clinical research and the law

This book provides a comprehensive resource for medical professionals on the various legal aspects involved in conducting clinical research. It encompasses legal and ethical issues such as duty of care, research malpractice and negligence, standards of care, informed consent, liability issues for In...

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Bibliographic Details
Main Author: Tereskerz, Patricia M. (Author)
Format: Book
Language:English
Published: Chichester, West Sussex John Wiley & Sons 2012
Subjects:
Online Access:Click Here to View Status and Holdings.
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520 # # |a This book provides a comprehensive resource for medical professionals on the various legal aspects involved in conducting clinical research. It encompasses legal and ethical issues such as duty of care, research malpractice and negligence, standards of care, informed consent, liability issues for Institutional Review Boards (IRB), conflicts of interest, insider trading and the disclosure and withholding of clinical trial results. It will also provide legal guidance on research contracts, setting up clinical trials and common legal pitfalls encountered in medical research 
650 1 2 |a Biomedical Research  |x legislation & jurisprudence  |z United States 
650 2 2 |a Biomedical Research  |x standards  |z United States 
650 2 2 |a Clinical Trials as Topic  |x legislation & jurisprudence  |z United States 
650 2 2 |a Clinical Trials as Topic  |x standards  |z United States 
650 2 2 |a Human Experimentation  |x legislation & jurisprudence  |z United States 
650 2 2 |a Human Experimentation  |x standards  |z United States 
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