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Titlebook: Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law; Daria Kim Book 2021 The Editor(s) (if applicable) and The Au

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發(fā)表于 2025-3-21 19:04:50 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law
影響因子2023Daria Kim
視頻videohttp://file.papertrans.cn/144/143703/143703.mp4
發(fā)行地址Provides a unique perspective on the regulation of access to clinical trial data as a case on knowledge externalities.Reveals limitations and inconsistencies of the current regulatory approach to acce
學(xué)科分類Munich Studies on Innovation and Competition
圖書封面Titlebook: Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law; Daria Kim Book 2021 The Editor(s) (if applicable) and The Au
影響因子.This book draws a unique perspective on the regulation of access to clinical trial data as a case on research and knowledge externalities. Notwithstanding numerous potential benefits for medical research and public health, many jurisdictions have struggled to ensure access to clinical trial data, even at the level of the trial results. Pro-access policy initiatives have been strongly opposed by research-based drug companies arguing that mandatory data disclosure impedes their innovation incentives. Conventionally, access to test data has been approached from the perspective of transparency and research ethics. The book offers a complementary view and considers access to individual patient-level trial data for .exploratory. analysis as a matter of research and innovation policy. Such approach appears to be especially relevant in the data-driven economy where digital data constitutes a valuable economic resource. The study seeks to define how the rules of access to clinical trialdata should be designed to reconcile the policy objectives of leveraging the research potential of data through secondary analysis, on the one hand, and protecting economic incentives of research-based drug
Pindex Book 2021
The information of publication is updating

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Legal Sources of Control Over and Access to Clinical Trial Data Under the EU Applicable Frameworkhin ist zu beobachten, da? die L?slichkeit der Fluoride mit der Kettenl?nge des Perfluoralkylrestes zunimmt. Da die Fluorierung sicherlich in der L?sungsphase abl?uft, darf bei den l?ngerkettigen Derivaten kein allzu gro?er Uberschu? an Fluor eingesetzt werden, um eine Weiterfluorierung zu vermeiden
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dents. The scope of this book is wide; it might be difficult for instructors and students to cover all of the chapters in a typical three credit-hour course. The instructor will need to assess his own situation and scheduling constraints. More or less time could be spent on chapters one through five, dependin978-1-4757-0413-6978-1-4757-0411-2
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Evaluating Legislative Options, July 1991, and during IAU Colloquium 151, Cordoba, Argentina, August 1991. The techniques discussed include simulations of stellar bright and dark spots, streams, partial and complete stellar disks, prominences, and other features characterizing active stars; modeling of polarization parameters; models that978-1-4612-7649-4978-1-4612-2742-7
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Final Conclusions and the Outlookresponses of plants considerably vary to different light treatments, and there is no specific pattern among the various species. Apart from its impact on plant regeneration responses up to the stage of ex vitro transfer, LED irradiation also significantly alters the cellular redox balance. LED-induc
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