Access to Medicines and Vaccines : (Record no. 308672)
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| 000 -LEADER | |
|---|---|
| fixed length control field | 10989nam a22004573i 4500 |
| 001 - CONTROL NUMBER | |
| control field | EBC6794041 |
| 005 - DATE AND TIME OF LATEST TRANSACTION | |
| control field | 20240122001459.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS | |
| fixed length control field | m o d | |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION | |
| fixed length control field | cr cnu|||||||| |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
| fixed length control field | 231124s2021 xx o ||||0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| International Standard Book Number | 9783030831141 |
| Qualifying information | (electronic bk.) |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER | |
| Canceled/invalid ISBN | 9783030831134 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (MiAaPQ)EBC6794041 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (Au-PeEL)EBL6794041 |
| 035 ## - SYSTEM CONTROL NUMBER | |
| System control number | (OCoLC)1321799487 |
| 040 ## - CATALOGING SOURCE | |
| Original cataloging agency | MiAaPQ |
| Language of cataloging | eng |
| Description conventions | rda |
| -- | pn |
| Transcribing agency | MiAaPQ |
| Modifying agency | MiAaPQ |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER | |
| Classification number | K4240-4343 |
| 100 1# - MAIN ENTRY--PERSONAL NAME | |
| Personal name | Correa, Carlos M. |
| 245 10 - TITLE STATEMENT | |
| Title | Access to Medicines and Vaccines : |
| Remainder of title | Implementing Flexibilities under Intellectual Property Law. |
| 250 ## - EDITION STATEMENT | |
| Edition statement | 1st ed. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Place of production, publication, distribution, manufacture | Cham : |
| Name of producer, publisher, distributor, manufacturer | Springer International Publishing AG, |
| Date of production, publication, distribution, manufacture, or copyright notice | 2021. |
| 264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
| Date of production, publication, distribution, manufacture, or copyright notice | �2022. |
| 300 ## - PHYSICAL DESCRIPTION | |
| Extent | 1 online resource (373 pages) |
| 336 ## - CONTENT TYPE | |
| Content type term | text |
| Content type code | txt |
| Source | rdacontent |
| 337 ## - MEDIA TYPE | |
| Media type term | computer |
| Media type code | c |
| Source | rdamedia |
| 338 ## - CARRIER TYPE | |
| Carrier type term | online resource |
| Carrier type code | cr |
| Source | rdacarrier |
| 505 0# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Intro -- Preface -- Contents -- Interpreting the Flexibilities Under the TRIPS Agreement -- 1 Introduction -- 2 Defining the TRIPS Flexibilities -- 3 TRIPS Flexibilities in WTO Jurisprudence -- 4 Interpretation of the TRIPS Agreement -- 4.1 Precedential Value of GATT/WTO Jurisprudence -- 4.2 Ordinary Meaning -- 4.3 Context -- 4.4 Object and Purpose -- 4.4.1 Legal Weight of the Doha Declaration -- 5 Conclusions -- References -- Intellectual Property Exhaustion and Parallel Imports of Pharmaceuticals: A Comparative and Critical Review -- 1 Introduction: The Relevance (and Resilience) of the Principle of Intellectual Property Exhaustion and Its Application to Pha... -- 2 Intellectual Property Exhaustion and Paralle Trade: General Considerations and Application to Pharmaceuticals -- 2.1 The Principle of Intellectual Property Exhaustion in International Trade: An Overview -- 2.2 Patent Exhaustion and the Debate on Parallel Trade of Pharmaceuticals -- 3 National Solutions to Patent Exhaustion and Parallel Trade of Pharmaceuticals -- 3.1 Selected Jurisdictions in Asia -- 3.2 Canada, United States, Australia, and New Zealand -- 3.3 Selected Jurisdictions in Latin America -- 3.4 European Union and Switzerland -- 3.5 Selected Jurisdictions in Africa -- 4 Overlapping Intellectual Property Rights and Parallel Trade of Pharmaceuticals -- 4.1 Overview of Overlapping Rights and Enforcement of Copyright to Parallel Imports -- 4.2 Enforcement of Trademark Rights to Parallel Imports of Pharmaceuticals -- 5 Conclusion: A Call for a Wider Application of the Flexibility of Article 6 of the TRIPS Agreement in Developing and Least De... -- References -- Compulsory Licenses and Government Use: Challenges and Opportunities -- 1 Introduction -- 2 Historical and Conceptual Roots -- 3 The TRIPS Framework -- 4 A Scan of the Use of TRIPS Flexibilities. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 5 A Tale of Two Countries -- 5.1 The Zimbabwean Case -- 5.1.1 Compulsory Licences -- 5.1.2 Government Use -- 5.1.3 Lessons -- 5.2 The South African Case -- 5.2.1 Legal Framework -- 5.2.2 AIDS Denialism -- 5.2.3 US Pressure -- 5.2.4 Judicial Deference -- 5.2.5 New IP Policy Phase I -- 6 Compulsory Licensing Options Under TRIPS -- 6.1 Expanded Grounds for Compulsory Licences -- 6.2 Government Use -- 6.3 Adequate Remuneration -- 6.4 Procedures for Compulsory Licensing Applications -- 6.5 Collaboration and Cooperation in the Issuance of CLs -- 6.6 A Compulsory Licensing Facility -- 7 Conclusion -- References -- Cases -- Statutes and Statutory Instruments -- Books -- Contributions to Edited Books -- Journal Articles -- Online Journals -- Command Articles and Law Commission Reports -- Websites and Blogs -- Access to CRISPR Genome Editing Technologies: Patents, Human Rights and the Public Interest -- 1 Introduction -- 2 The Human Genome -- 3 The CRISPR-Cas9 Genome Editing Technique -- 4 Lulu and Nana: The Chinese Genome-Edited Twins ``Immune from HIV�� -- 5 Patenting the CRISPR-Cas9 Genome Editing Breakthrough -- 6 Excluding Genome Editing Technologies from Patentability -- 7 International Human Rights Law and Genome Editing -- 8 International Initiatives on the Regulation and Governance of Gene Editing -- 9 Concluding Remarks -- References -- Bolar Exception -- 1 Exceptions to Patent Rights -- 2 Rationale for the Bolar Exception -- 2.1 Marketing Authorization of Medical Products -- 2.2 Relationship of Patent Protection, Marketing Authorization and Supplementary Legal Protection -- 2.3 Role of Generic and Biosimilar Competition in Promoting Access -- 3 History of the Bolar Exception -- 4 Consistency with Article 30 of the TRIPS Agreement -- 5 Crafting National Legal Frameworks for the Bolar Exception -- 6 India Bolar Exception: Recent Developments. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 7 Conclusions -- References -- Patent Oppositions in India -- 1 Introduction -- 2 Patent Oppositions in India -- 2.1 Gleevec Opposition -- 2.2 Valcyte Opposition -- 2.3 Herceptin Opposition -- 2.4 Zykadia Opposition -- 2.5 The Viread Oppositions -- 2.6 Kaletra Opposition -- 2.7 Reyataz Opposition -- 2.8 Combivir Opposition -- 2.9 Trizivir Opposition -- 2.10 Ziagen Opposition -- 2.11 Isentress Opposition -- 2.12 Sanofi TB Drugs Oppositions -- 2.13 Veklury Opposition -- 3 Pendency of Oppositions in the Indian Patent Office -- 3.1 Pre-grant Oppositions -- 3.2 Post-grant Oppositions -- 3.3 Pendency at the Intellectual Property Appellate Board (IPAB) -- 3.4 Impact of Pendency -- 4 Conclusion -- Annex: Opposition Pendency Data for the Period 2007-08 to 2019-2020 -- References -- Protection of Clinical Test Data and Public Health: A Proposal to End the Stronghold of Data Exclusivity -- 1 Introduction: Test Data and Efficacy, Safety and Quality of Medicines -- 2 Generic and Biosimilar Medicine Marketing Approval and the Use of Test Data -- 3 Rationale for Data Exclusivity -- 3.1 Data Exclusivity and Patents -- 3.2 Data Exclusivity�s Effectiveness in Stimulating Innovation -- 4 History of Data Exclusivity -- 4.1 Data Exclusivity in the United States -- 4.2 Data Exclusivity in the European Union -- 4.3 Protection of Test Data and the Rules of the World Trade Organization -- 5 Data Exclusivity in Free Trade Agreements (FTAs) -- 6 Data Exclusivity and TRIPS Flexibilities -- 6.1 Compulsory Licensing and Government Use in Drug Procurement -- 6.2 Data Exclusivity and Compulsory Licensing -- 6.3 Remedies to Data Exclusivity Barriers and Compulsory Licensing -- 6.4 Data Exclusivity Waivers in FTAs -- 6.5 EU Medicines Regulation and Compulsory Licensing -- 6.6 EU Data Exclusivity Waiver and Compulsory Licence for Export. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 6.7 Data Exclusivity Waivers in Voluntary Patent Licences -- 6.8 Public Health Measures, Data Exclusivity and Competition Law -- 6.9 EU Law Needs an Explicit Data Exclusivity Waiver -- 7 Conclusion and Recommendations -- References -- Courts and Pharmaceutical Patents: From Formalist Positivism to the Emergence of a Global Law -- 1 Introduction -- 2 Assessing the Role of Courts in TRIPS Flexibilities As Forms of Structural Change -- 3 Access and Innovation in Legal Discourse: From Opposition to Coexistence -- 4 Trastuzumab High Price Litigation in Brazil -- 5 The Sofosbuvir Case in Brazil -- 6 Theoretical Conclusions on the Role of Courts in IP Based on the Concrete Cases -- 7 Concluding Remarks -- References -- Robust Patent Examination or Deep Harmonization? Cooperation and Work Sharing Between Patent Offices -- 1 Introduction -- 2 Patent Examination: A Critical TRIPS Flexibility -- 3 Approaches to Patent Harmonisation -- 3.1 Normative Approaches -- 3.2 Persuasive Approaches -- 3.2.1 Technical Assistance -- 3.2.2 Quality of Patents -- 4 PCT Reforms -- 4.1 Working Group on PCT Reforms -- 4.1.1 Establishment of a Written Opinion on Patentability to Accompany the International Search Report -- 4.1.2 Automatic Designation of all PCT Contracting Parties for National Phase Entry -- 4.1.3 Establishment of an Optional Supplementary International Search -- 4.2 New PCT Working Group -- 5 Work Sharing Arrangements Between Patent Offices -- 5.1 Trilateral Cooperation -- 5.2 IP5 Cooperation -- 5.3 The Vancouver Group -- 5.4 PROSUR -- 5.5 ASPEC -- 5.6 IP BRICS -- 5.7 Patent Prosecution Highway -- 6 Opportunities and Challenges -- 6.1 South-South Cooperation -- 6.2 Safeguarding and Utilising TRIPS Flexibilities -- 6.3 Use of Technology -- 6.4 Administrative Law Oversight -- 7 Conclusion -- References. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | Intellectual Property Rights (IPRs), Competition Law and Excessive Pricing of Medicines -- 1 Introduction -- 2 TRIPS and Competition Policy: Orientations and Enforcement Trends in the Pharmaceutical Sector -- 2.1 The Interface Between IPRs and Competition Law -- 2.2 TRIPS and Competition Law: Competition Law as Flexibility Tool -- 2.3 Enforcement Trends of Competition Law in the Pharmaceutical Sector -- 3 Excessive Pricing of Pharmaceuticals: An Emerging Enforcement Trend -- 3.1 Pricing of Pharmaceuticals and IPRs -- 3.2 Overview of the Case Law on Excessive Pricing of Pharmaceuticals -- 3.3 Competition and IP Issues Raised by the Case Law on Excessing Pricing of Pharmaceuticals -- 3.3.1 IP, Patent Term and Excessive Pricing of Pharmaceuticals -- 3.3.2 Competition Law and Excessive Pricing of Pharmaceuticals: Market Conditions and Pricing -- Market Power, Size of the Market and High Pricing -- Absence of Substitutability and High Pricing of Pharmaceuticals -- Consumer Choice/Behavior (Rationality) and the Specificity of Pharmaceuticals -- The Issue of the Determination of an Excessive Price -- 4 Excessive Pricing of Pharmaceuticals and TRIPS Flexibilities: Lessons from the Excessive Prices Cases -- 5 Conclusions -- References -- The Impact of `TRIPS-Plus� Rules on the Use of TRIPS Flexibilities: Dealing with the Implementation Challenges -- 1 Introduction -- 2 Expensive Medicines: National Implications and Global Challenges -- 3 Unequal Investment and More Monopoly -- 4 The Double Taxation of Society -- 5 More Pharmaceutical Patents, Weaker Innovation -- 6 Increased IP Standards: From TRIPS-Minus to TRIPS-Plus -- 6.1 The Flexibilities Explained -- 6.2 Putting the Flexibilities into Use -- 6.3 The Shift Towards TRIPS-Plus -- 6.4 Impact and Examples of TRIPS-Plus Obligations -- 7 What Could Be Done and What Is Done? -- 7.1 Australia -- 7.2 Chile. |
| 505 8# - FORMATTED CONTENTS NOTE | |
| Formatted contents note | 7.3 What Others Are Doing and How They Are Doing It?. |
| 588 ## - SOURCE OF DESCRIPTION NOTE | |
| Source of description note | Description based on publisher supplied metadata and other sources. |
| 590 ## - LOCAL NOTE (RLIN) | |
| Local note | Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, 2023. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries. |
| 655 #4 - INDEX TERM--GENRE/FORM | |
| Genre/form data or focus term | Electronic books. |
| 700 1# - ADDED ENTRY--PERSONAL NAME | |
| Personal name | Hilty, Reto M. |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY | |
| Relationship information | Print version: |
| Main entry heading | Correa, Carlos M. |
| Title | Access to Medicines and Vaccines |
| Place, publisher, and date of publication | Cham : Springer International Publishing AG,c2021 |
| International Standard Book Number | 9783030831134 |
| 797 2# - LOCAL ADDED ENTRY--CORPORATE NAME (RLIN) | |
| Corporate name or jurisdiction name as entry element | ProQuest (Firm) |
| 856 40 - ELECTRONIC LOCATION AND ACCESS | |
| Uniform Resource Identifier | <a href="https://ebookcentral.proquest.com/lib/bacm-ebooks/detail.action?docID=6794041">https://ebookcentral.proquest.com/lib/bacm-ebooks/detail.action?docID=6794041</a> |
| Public note | Click to View |
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