Developing a national registry of pharmacologic and biologic clinical trials : workshop report /
Clasificación: | Libro Electrónico |
---|---|
Autor Corporativo: | |
Formato: | Electrónico eBook |
Idioma: | Inglés |
Publicado: |
Washington, D.C. :
National Academies Press,
©2006.
|
Temas: | |
Acceso en línea: | Texto completo |
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