Ebook Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition (4), Band 4)
Beschreibung Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition (4), Band 4)
/3662496542
This book explores the concept of test data exclusivity protection for pharmaceuticals. Focusing on Art 39(3) of the WTO Agreement on Trade-Related Aspects of Intellectual Property Rights (TRIPS Agreement) and relevant provisions in selected free trade agreements (FTA) and national laws, it combines normative, historical, comparative and economic analysis of test data exclusivity protection.At the heart of this book is the novel and original Index of Data Exclusivity and Access (IDEAS), which analyzes the effectiveness of test data exclusivity provisions in FTAs and national laws both on the strength of exclusivity as well as on access to medicine. IDEAS provides a framework for the assessment of current test data exclusivity protection standards on the basis of their proximity to Article 39(3) of the TRIPS Agreement, the scope of exclusivity and the flexibilities in FTAs, and subsequently in national laws. This book aims to broaden national and international policy makers’ grasp of the various nuances of test data exclusivity protection. Furthermore, it provides practical recommendations with regard to designing an appropriate legal system with a strong focus on promoting access to medicine for all.
Lesen Sie das Buch Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition (4), Band 4)
Access to Medicine Versus Test Data Exclusivity ~ Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition, Band 4) / Shaikh, Owais H. / ISBN: 9783662570210 / Kostenloser Versand für alle Bücher mit Versand und Verkauf duch .
Access to Medicine Versus Test Data Exclusivity ~ Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition (4), Band 4) / Shaikh, Owais H. / ISBN: 9783662496541 / Kostenloser Versand für alle Bücher mit Versand und Verkauf duch .
Access to Medicine Versus Test Data Exclusivity ~ Access to Medicine Versus Test Data Exclusivity: Safeguarding Flexibilities Under International Law (Munich Studies on Innovation and Competition, Band 4) von Owais H. Shaikh. Taschenbuch. Details (Deutschland) (siehe auch: Kindle Ausgabe) Details (siehe auch: eBook (Kindle)) Details (Großbritannien) (siehe auch: eBook (Kindle)) ISBN-13: 978-3-662-57021-0. ISBN-10: 3-662-57021-1. Springer .
Access To Medicine Versus Test Data Exclusivity ~ access to medicine versus test data exclusivity safeguarding flexibilities under international law munich studies Sep 07, 2020 Posted By Horatio Alger, Jr. Media TEXT ID f1130dc32 Online PDF Ebook Epub Library member log in you must be logged into bookshare to access this title learn about membership options or view our freely available titles synopsis this book explores the
Series - Max Planck Institute for Innovation and Competition ~ Volume 4. Owais H. Shaikh Access to Medicine Versus Test Data Exclusivity - Safeguarding Flexibilities Under International Law Springer, Berlin; Heidelberg 2016, XVI + 256 Seiten, ISBN 978-3-662-49654-1. DOI. Volume 3 Busch, Anna Friederike Protection of Traditional Cultural Expressions in Latin America. A Legal and Anthropological Study
Frequently Asked Questions on Patents and Exclusivity / FDA ~ Exclusivity was designed to promote a balance between new drug innovation and greater public access to drugs that result from generic drug competition. Back to Top 2.
Biosimilar medicines: Overview / European Medicines Agency ~ Biosimilar competition should improve patient access to safe and effective biological medicines with proven quality. Comparison of data requirements for approval of a biosimilar versus the reference medicine. Biosimilars can only be authorised once the period of data exclusivity on the 'reference' biological medicine has expired.
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