A clinical trials manual from the Duke Clinical Research Institute : lessons from a horse named Jim /

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Bibliographic Details
Main Author: Liu, Margaret B.
Corporate Author: Duke Clinical Research Institute
Other Authors: Davis, Kate (Kate G.)
Format: Book
Language:English
Published: Chichester, West Sussex, UK ; Hoboken, NJ : Wiley-Blackwell, 2010.
Edition:2nd ed.
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Online Access:Publisher description
Table of contents only
Contributor biographical information
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Table of Contents:
  • Lessons from a horse named Jim and other events in history affecting the regulation of clinical research
  • The process : developing new drugs, biologics, and devices
  • Good clinical practice and the regulations
  • Informed consent and the regulations
  • Institutional review boards
  • Adverse events and unanticipated problems involving risks to subjects and others
  • Monitoring, audits, and inspections
  • The principal investigator, the clinical research coordinator, and the study site
  • The protocol
  • Study feasibility : reviewing a specific protocol
  • Study activities
  • Study documents/essential documents
  • Management of study drugs, biologics, and devices
  • Managing clinical trial data
  • Global health and international trials.