Clinical Trial Registries
A Practical Guide for Sponsors and Researchers of Medicinal Products
(Sprache: Englisch)
ICMJE editors and other journal editors require registration of clinical trial information on publicly available Web sites before enrollment of study subjects. Not only does this book discuss the genesis of these requirements, it also provides practical...
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Klappentext zu „Clinical Trial Registries “
ICMJE editors and other journal editors require registration of clinical trial information on publicly available Web sites before enrollment of study subjects. Not only does this book discuss the genesis of these requirements, it also provides practical information for researchers and sponsors on how to establish a workflow for a clinical registry project, how to file to a registry, and how to post results.
Inhaltsverzeichnis zu „Clinical Trial Registries “
Clinical trial registries and publication of results.- The journal editor's perspective.- Industry perspective on public clinical trial registries and results databases.- Public and patient usage and expectations for clinical trial registries.- Building a global culture of trial registration.- The Japanese perspective on registries and a review of clinical trial process in Japan.- Transparency and validity of pharmaceutical research.- A project management approach to the planning and execution of clinical trial registries.- Biopharmaceutical companies tackle clinical trial transparency.- In search of 'Clinical Trial Register - Version 2.0'.- Clinical trial registries and study results databases.- Annotated bibliography of important papers
Bibliographische Angaben
- 2006, 2006, 194 Seiten, Maße: 12,7 x 19 cm, Kartoniert (TB), Englisch
- Herausgegeben: MaryAnn Foote
- Verlag: Springer
- ISBN-10: 3764375787
- ISBN-13: 9783764375782
- Erscheinungsdatum: 16.08.2006
Sprache:
Englisch
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