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Intellectual property rights in pharmaceutical test dataorigins, globalisation and impact /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Intellectual property rights in pharmaceutical test databy Adam Buick.
Reminder of title:	origins, globalisation and impact /
Author:	Buick, Adam.
Published:	Cham :Springer International Publishing :2023.
Description:	1 online resource (xvi, 227 p.) :ill., digital ;24 cm.
Contained By:	Springer Nature eBook
Subject:	Intellectual property (International law)
Online resource:	https://doi.org/10.1007/978-3-031-29436-5
ISBN:	9783031294365$q(electronic bk.)

Intellectual property rights in pharmaceutical test dataorigins, globalisation and impact /
Buick, Adam.

Intellectual property rights in pharmaceutical test dataorigins, globalisation and impact /[electronic resource] :by Adam Buick. - Cham :Springer International Publishing :2023. - 1 online resource (xvi, 227 p.) :ill., digital ;24 cm.

Chapter 1 - Introduction -- Chapter 2 - An overview of the protection of submitted test data -- Chapter 3 - The origins of test data exclusivity -- Chapter 4 - The protection of submitted test data and the TRIPS Agreement -- Chapter 5 - The globalisation of test data exclusivity -- Chapter 6 - Approaches to the Implementation of the Protection of Submitted Test Data -- Chapter 7 - The impact of test data exclusivity -- Chapter 8 - The Impact of Test Data Exclusivity on Measures for the Protection of Public Health -- Chapter 9 - Conclusion.

This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early 1980s, how they have globalised over the past four decades, and what impact they have had upon access to medicine. This book makes a number of significant and original contributions to the literature around the protection of submitted test data. First, the book draws upon the theory of regulatory globalisation to provide an explanation of how intellectual property rights in submitted pharmaceutical test data have become nearly ubiquitous in the legal systems of most major economies. Second, through a comprehensive analysis and synthesis of provisions on the protection of submitted test data in free trade agreements, as well as a comparison of a range of national approaches to the protection of submitted test data, it reveals the broader global regulatory pattern that has given rise to these intellectual property rights. Third, by analysing data on drug approvals in the US, it provides an empirical insight into the impact of test data exclusivity in national pharmaceutical markets. Fourth, the book covers a number of developments regarding test data exclusivity that have occurred as a result of responses to the COVID-19 pandemic, both at the national level as well as at the World Trade Organisation (WTO) This book will appeal to academics researching the intersection of intellectual property and the life sciences, civil society activists working to promote access to medicines, and students (particularly those at the post-graduate level) studying the relationship between intellectual property and medicine.

ISBN: 9783031294365$q(electronic bk.)

Standard No.: 10.1007/978-3-031-29436-5doiSubjects--Topical Terms:

175439
Intellectual property (International law)

LC Class. No.: K1401

Dewey Class. No.: 346.048

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520 $a This book considers the intellectual property protection of clinical test data that has been submitted to governments, in particular through test data exclusivity rights. It focuses on how these intellectual property rights first emerged in the early 1980s, how they have globalised over the past four decades, and what impact they have had upon access to medicine. This book makes a number of significant and original contributions to the literature around the protection of submitted test data. First, the book draws upon the theory of regulatory globalisation to provide an explanation of how intellectual property rights in submitted pharmaceutical test data have become nearly ubiquitous in the legal systems of most major economies. Second, through a comprehensive analysis and synthesis of provisions on the protection of submitted test data in free trade agreements, as well as a comparison of a range of national approaches to the protection of submitted test data, it reveals the broader global regulatory pattern that has given rise to these intellectual property rights. Third, by analysing data on drug approvals in the US, it provides an empirical insight into the impact of test data exclusivity in national pharmaceutical markets. Fourth, the book covers a number of developments regarding test data exclusivity that have occurred as a result of responses to the COVID-19 pandemic, both at the national level as well as at the World Trade Organisation (WTO) This book will appeal to academics researching the intersection of intellectual property and the life sciences, civil society activists working to promote access to medicines, and students (particularly those at the post-graduate level) studying the relationship between intellectual property and medicine.
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