Clinical research coordinator handbook /

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Bibliographic Details
Main Author: Norris, Deborrah
Format: Book
Language:English
Published: Medford, NJ : Plexus Pub., c2009.
Edition:4th ed.
Subjects:
Online Access:Visit NHRC Library
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100 1 |a Norris, Deborrah.  |9 3723 
245 1 0 |a Clinical research coordinator handbook /  |c Deborrah Norris. 
250 |a 4th ed. 
260 |a Medford, NJ :  |b Plexus Pub.,  |c c2009. 
300 |a x, 157 p.  |b ill. ;  |c 28 cm. 
500 |a SEN.: 272/47 No.:01 FY: 2072/73 
504 |a Includes bibliographical references. 
505 0 |a Federal regulations governing the obligations of clinical investigators of regulated articles -- The clinical research organization -- Investigator responsibilities -- Duties of the clinical research coordinator -- The creation of study source documents -- Obtaining informed consent and assent approval -- Pertinent forms and study records -- The prestudy site visit -- Recruiting and enrolling subjects -- Conducting the study and keeping records -- Preparing for an FDA audit -- Clinical research : potential liability -- Writing the study sumary -- Achieving credibility and recognition as a Clinical Research Coordinator -- Electronic data capture and clinical trials. 
650 0 |a Clinical trials  |z United States  |v Handbooks, manuals, etc.  |9 3724 
650 1 2 |a Clinical Trials as Topic  |x standards  |z United States  |v Handbooks.  |9 3725 
650 2 2 |a Clinical Trials as Topic  |x methods  |z United States  |v Handbooks.  |9 3726 
650 2 2 |a Records as Topic  |x standards  |z United States  |v Handbooks.  |9 3727 
650 2 2 |a Research Design  |x standards  |z United States  |v Handbooks.  |9 3728 
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