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|a Developing a national registry of pharmacologic and biologic clinical trials :
|b workshop report /
|c Committee on Clinical Trial Registries, Board on Health Sciences Policy, Institute of Medicine of the National Academies.
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|a Washington, D.C. :
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|c ©2006.
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|a Includes bibliographical references (pages 47-48).
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|a Electronic reproduction.
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|a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.
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|a 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
|
| 505 |
8 |
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|a 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
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|a Institute of Medicine (U.S.).
|b Committee on Clinical Trial Registries.
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|i Print version:
|t Developing a national registry of pharmacologic and biologic clinical trials.
|d Washington, D.C. : National Academies Press, ©2006
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