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Electronic Resource

Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law

Kim, Daria - Personal Name;

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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 companies, on the other hand. Overall, it is argued that the mainstream innovation-based justification for exclusive control over the outcomes of research and development can hardly rationalise trial sponsors’ control over primary data from trials. Instead, access to such data and its robust analysis should be prioritised.


Availability
Inventory Code Barcode Call Number Location Status
2108000096EB0005484344.04 Kim aCentral Library (OPAC)Available
Detail Information
Series Title
-
Call Number
344.04 Kim a
Publisher
Switzerland : Springer Cham., 2021
Collation
xviii, 300p.:ill
Language
English
ISBN/ISSN
978-3-030-86778-2
Classification
344.04
Content Type
Ebook
Media Type
-
Carrier Type
online resource
Edition
1
Subject(s)
Medical law
Specific Detail Info
-
Statement of Responsibility
BRF
Other version/related
TitleEditionLanguage
Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law1en
File Attachment
  • Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law
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