Tabla de Contenidos:
  • FrontMatter
  • Independent Report Reviewers
  • Foreword
  • Preface
  • Contents
  • List of Tables
  • 1 Summary
  • 2 The Need for Clinical Trial Registries
  • 3 Current Registry Activities
  • 4 Content of a Clinical Trial Registry
  • 5 Implementation Issues
  • 6 Conclusion and Next Steps
  • References
  • APPENDIXES
  • A Participants and Invited Experts Between December 1, 2004, and June 27, 2005
  • B Workshop Agenda, Speakers, Panelists, and Participants: June 27, 2005
  • C Section 113 of the Food and Drug Administration Modernization Act of 1997 and Guidance for Industry: Information Programs on Clinical Trials for Serious or Life- Threatening Diseases and Conditions. U.S. Department of Health and Human Services. D Published Journal Editorials
  • E Joint Position on the Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases
  • F Illustrative Data Fields for the Results Summary (based on ICH E3 template)
  • G Biographical Sketches of Committee Members