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

Overview of attention for book
Cover of 'Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction
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    Chapter 2 The Context and the Problem
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    Chapter 3 Secondary Analysis of Individual Patient-Level Clinical Trial Data: A Primer
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    Chapter 4 Legal Sources of Control Over and Access to Clinical Trial Data Under the EU Applicable Framework
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    Chapter 5 Implications of IPD Disclosure for Statutory Innovation Incentives
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    Chapter 6 Defining the Intervention Logic of Access-To-Data Measures: A Problem Analysis
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    Chapter 7 Access to Clinical Trial Data as a Case on R&D Externalities: A Theoretical Framework
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    Chapter 8 IPD as a Research Resource: Exclusively Controlled or Readily Accessible?
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    Chapter 9 Evaluating Legislative Options
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    Chapter 10 Final Conclusions and the Outlook
Attention for Chapter 4: Legal Sources of Control Over and Access to Clinical Trial Data Under the EU Applicable Framework
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Chapter title
Legal Sources of Control Over and Access to Clinical Trial Data Under the EU Applicable Framework
Chapter number 4
Book title
Access to Non-Summary Clinical Trial Data for Research Purposes Under EU Law
Published by
Springer, Cham, October 2021
DOI 10.1007/978-3-030-86778-2_4
Book ISBNs
978-3-03-086777-5, 978-3-03-086778-2
Authors

Kim, Daria

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 1 Mendeley reader of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 1 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 100%
Readers by discipline Count As %
Social Sciences 1 100%

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