Description

Book Synopsis
Developing a National Registry of Pharmacologic and Biologic Clinical Trials: Workshop Report (2006)

Table of Contents
1 Front Matter; 2 1 Summary; 3 2 The Need for Clinical Trial Registries; 4 3 Current Registry Activities; 5 4 Content of a Clinical Trial Registry; 6 5 Implementation Issues; 7 6 Conclusion and Next Steps; 8 References; 9 Appendix A Participants and Invited Experts - Between December 1, 2004 and June 27, 2005; 10 Appendix B Workshop Agenda, Speakers, Panelists, and Participants - June 27, 2005; 11 Appendix C Sec. 113 of the Food and Drug Administration Modernization Act of 1997; Guidance for Industry: Information Programs on Clinical Trials..; 12 Appendix D Published Journal Editorials; 13 Appendix E Joint Position on the Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases; 14 Appendix F Illustrative Data Fields for the Results Summary; 15 Appendix G Biographical Sketches of Committee Members

Developing a National Registry of Pharmacologic and Biologic Clinical Trials Workshop Report

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    A Paperback by Board on Health Sciences Policy, Board on Health Sciences Policy, Committee on Clinical Trial Registries

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      View other formats and editions of Developing a National Registry of Pharmacologic and Biologic Clinical Trials Workshop Report by Board on Health Sciences Policy

      Publisher: National Academies Press
      Publication Date: 7/12/2006 12:00:00 AM
      ISBN13: 9780309100786, 978-0309100786
      ISBN10: 030910078X

      Description

      Book Synopsis
      Developing a National Registry of Pharmacologic and Biologic Clinical Trials: Workshop Report (2006)

      Table of Contents
      1 Front Matter; 2 1 Summary; 3 2 The Need for Clinical Trial Registries; 4 3 Current Registry Activities; 5 4 Content of a Clinical Trial Registry; 6 5 Implementation Issues; 7 6 Conclusion and Next Steps; 8 References; 9 Appendix A Participants and Invited Experts - Between December 1, 2004 and June 27, 2005; 10 Appendix B Workshop Agenda, Speakers, Panelists, and Participants - June 27, 2005; 11 Appendix C Sec. 113 of the Food and Drug Administration Modernization Act of 1997; Guidance for Industry: Information Programs on Clinical Trials..; 12 Appendix D Published Journal Editorials; 13 Appendix E Joint Position on the Disclosure of Clinical Trial Information via Clinical Trial Registries and Databases; 14 Appendix F Illustrative Data Fields for the Results Summary; 15 Appendix G Biographical Sketches of Committee Members

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