Clinical research coordinator handbook / Deborrah Norris.
Material type:![Text](/opac-tmpl/lib/famfamfam/BK.png)
- 9780937548707
- Clinical trials -- United States -- Handbooks, manuals, etc
- Clinical Trials as Topic -- standards -- United States -- Handbooks
- Clinical Trials as Topic -- methods -- United States -- Handbooks
- Records as Topic -- standards -- United States -- Handbooks
- Research Design -- standards -- United States -- Handbooks
- 610.72 22
- R853.C55 N67 2009
- QV 39
Item type | Current library | Call number | Status | Date due | Barcode |
---|---|---|---|---|---|
![]() |
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.
There are no comments on this title.