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

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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 7: Access to Clinical Trial Data as a Case on R&D Externalities: A Theoretical Framework
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Chapter title
Access to Clinical Trial Data as a Case on R&D Externalities: A Theoretical Framework
Chapter number 7
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_7
Book ISBNs
978-3-03-086777-5, 978-3-03-086778-2
Authors

Kim, Daria

View on publisher site

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