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Clinical research coordinator handbook / Deborrah Norris.

By: Material type: TextTextPublication details: Medford, NJ : Plexus Pub., c2009.Edition: 4th edDescription: x, 157 p. ill. ; 28 cmISBN:
  • 9780937548707
Subject(s): DDC classification:
  • 610.72 22
LOC classification:
  • R853.C55 N67 2009
NLM classification:
  • QV 39
Online resources:
Contents:
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.
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Holdings
Item type Current library Call number Status Date due Barcode
Books Books Nepal Health Research Council Book Cart QV 39/NOR/2009 (Browse shelf(Opens below)) Available 001979

SEN.: 272/47 No.:01 FY: 2072/73

Includes bibliographical references.

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.

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