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Titlebook: Clinical Trial Registries; A Practical Guide fo MaryAnn Foote Book 2006 Birkh?user Basel 2006 clinical trial.drug.drug sponsor.medicinal pr

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發(fā)表于 2025-3-21 19:29:19 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Clinical Trial Registries
副標題A Practical Guide fo
編輯MaryAnn Foote
視頻videohttp://file.papertrans.cn/229/228255/228255.mp4
概述Numerous practical hints for everyone involved in registration of clinical projects.Useful Web-addresses.Different countries’ regulations are considered.Includes supplementary material:
圖書封面Titlebook: Clinical Trial Registries; A Practical Guide fo MaryAnn Foote Book 2006 Birkh?user Basel 2006 clinical trial.drug.drug sponsor.medicinal pr
描述.Clinical Trial Registries: A Practical Guide for Sponsors and Researchers of Medicinal Products is a necessary addition to the library of all researchers who plan to publish their results in top-tier, peer-reviewed journals. ICMJE editors and other journal editors require registration of clinical trial information on publicly available Web sites before enrollment of study subjects and some countries and regions also require this information, as well as timely publication of study results. 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. More than 25 current Web addresses for registries are provided as well as?a comprehensive annotated bibliography of papers on the topic of clinical trial registries. This book is a valuable source of information for all sponsors of medicinal products..
出版日期Book 2006
關(guān)鍵詞clinical trial; drug; drug sponsor; medicinal product; pharmaceutical research; pharmacology; registries; r
版次1
doihttps://doi.org/10.1007/978-3-7643-7583-6
isbn_softcover978-3-7643-7578-2
isbn_ebook978-3-7643-7583-6
copyrightBirkh?user Basel 2006
The information of publication is updating

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發(fā)表于 2025-3-21 21:39:46 | 只看該作者
Book 2006hers who plan to publish their results in top-tier, peer-reviewed journals. ICMJE editors and other journal editors require registration of clinical trial information on publicly available Web sites before enrollment of study subjects and some countries and regions also require this information, as
板凳
發(fā)表于 2025-3-22 03:04:37 | 只看該作者
Book 2006 than 25 current Web addresses for registries are provided as well as?a comprehensive annotated bibliography of papers on the topic of clinical trial registries. This book is a valuable source of information for all sponsors of medicinal products..
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發(fā)表于 2025-3-22 06:24:46 | 只看該作者
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發(fā)表于 2025-3-22 11:53:12 | 只看該作者
MaryAnn FooteNumerous practical hints for everyone involved in registration of clinical projects.Useful Web-addresses.Different countries’ regulations are considered.Includes supplementary material:
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發(fā)表于 2025-3-22 16:29:59 | 只看該作者
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發(fā)表于 2025-3-23 06:11:26 | 只看該作者
Transparency and validity of pharmaceutical research, clinical research goes forward with the full knowledge that trial design and results will be critically examined. A product will not be licensed for marketing nor will an advertising claim be permitted unless the data support it.
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