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- 2009030187 contributor B11429161.
- 2009030187 created "c2009.".
- 2009030187 date "2009".
- 2009030187 date "c2009.".
- 2009030187 dateCopyrighted "c2009.".
- 2009030187 description "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.".
- 2009030187 description "Includes bibliographical references.".
- 2009030187 extent "x, 157 p.".
- 2009030187 identifier "9780937548707".
- 2009030187 issued "2009".
- 2009030187 issued "c2009.".
- 2009030187 language "eng".
- 2009030187 publisher "Medford, NJ : Plexus Pub.,".
- 2009030187 spatial "United States".
- 2009030187 subject "610.72 22".
- 2009030187 subject "Clinical Trials as Topic methods United States Handbooks.".
- 2009030187 subject "Clinical Trials as Topic standards United States Handbooks.".
- 2009030187 subject "Clinical trials United States Handbooks, manuals, etc.".
- 2009030187 subject "QV 39 N854c 2009".
- 2009030187 subject "R853.C55 N67 2009".
- 2009030187 subject "Records as Topic standards United States Handbooks.".
- 2009030187 subject "Research Design standards United States Handbooks.".
- 2009030187 tableOfContents "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.".
- 2009030187 title "Clinical research coordinator handbook / Deborrah Norris.".
- 2009030187 type "text".