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ویرایش:
نویسندگان: Paul England
سری:
ISBN (شابک) : 9781509947645, 9781509947669
ناشر: Hart Publishing
سال نشر: 2022
تعداد صفحات: [659]
زبان: English
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود)
حجم فایل: 8 Mb
در صورت تبدیل فایل کتاب A Practitioner’s Guide to European Patent Law: For National Practice and the Unified Patent Court به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.
توجه داشته باشید کتاب راهنمای یک پزشک برای قانون ثبت اختراع اروپا: برای رویه ملی و دادگاه یکپارچه ثبت اختراع نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.
این ویرایش جدید یک راهنمای جامع و عملی برای قانون ثبت اختراع اروپا - یک \"ius commune\" است. این کتاب حوزههای سازگاری و تفاوت بین تأثیرگذارترین حوزههای قضایی حقوق ثبت اختراع اروپا را برجسته میکند: اداره ثبت اختراع اروپا، انگلستان و ولز، فرانسه، آلمان و هلند. این کتاب همچنین بینش هایی را از مناطق دورتر، با مشارکت سایر حوزه های قضایی بسیار فعال، از جمله ایتالیا، سوئد، دانمارک و سوئیس به دست می آورد. این کتاب به طور منحصر به فردی به قانون ثبت اختراع اروپا بر اساس حوزه موضوعی می پردازد و رویکردهای کلیدی ملی و EPO را با هم به جای ملت به کشور ارزیابی می کند. هر فصل به تشریح زمینه مشترک بین رویکردهای ملی می پردازد و راهنمایی برای کاربرد احتمالی قانون ثبت اختراع اروپایی در دادگاه های ملی و UPC در آینده ارائه می دهد. علاوه بر محتوای کشورهای جدید، ویرایش دوم شامل فصول جدیدی است که به جنبه های اساسی FRAND، اعلامیه ها و شواهد اختصاص یافته است. همچنین یک تفسیر گسترده در مورد ساخت و ساز، از جمله اصطلاحات رایج مورد استفاده در ادعاهای ثبت اختراع وجود دارد. برای هر کسی که در زمینه حقوق ثبت اختراع اروپا کار می کند باید بخوانید.
This new edition is a comprehensive and practical guide to European patent law – a \'ius commune\'. The book highlights the areas of consistency and difference between the most influential European patent law jurisdictions: the European Patent Office, England and Wales, France, Germany, and the Netherlands. The book also draws insights from further afield, with contributions from other, very active, patent jurisdictions, including Italy, Sweden, Denmark, and Switzerland. Uniquely, the book addresses European patent law by subject matter area, assessing the key national and EPO approaches together rather than nation by nation. Each chapter outlines the common ground between the national approaches and provides a guide for the possible application of European patent law in national courts and the UPC in the future. In addition to featuring content on new countries, the second edition includes new chapters dedicated to the substantive aspects of FRAND, declarations, and evidence. There is also an expanded commentary on construction, including common terms used in patent claims. A must-read for anyone working in the field of European patent law.
Explanatory Note on the Second Edition and Acknowledgements Contents Abbreviations Table of Cases Table of EU and International Material Table of National Materials Introduction I. Towards a ius commune of Patent Law II. The Purpose of this Book 1. The Skilled Person and their Common General Knowledge I. The Skilled Person or Team II. Common General Knowledge III. Key Issues for the UPC 2. Scope of Protection of Patent Claims I. Statutory Basis II. Principles of Construction III. General Principles of National Law on the Doctrine of Equivalents IV. The Role of a 'Formstein Defence' V. The Role of the Prosecution File VI. Particular Terms and Forms of Claim VII. Numerical Ranges VIII. Case Comparison – The Pemetrexed Decisions IX. Key Issues for the UPC 3. Direct Infringement I. Statutory Basis II. Liability III. Territoriality IV. Product Claims (Article 25(a) CPC 1989) V. Process Claims (Article 25(b) CPC 1989) VI. Products Made by an Infringing Process (Article 25(c) CPC 1989) VII. Processes for Obtaining New Products VIII. Second Medical Use Claim Infringement IX. Infringement of DNA Sequences X. Unjustified Threats XI. Key Issues for the UPC 4. Indirect Infringement I. Statutory Basis II. Means Relating to an Essential Element of the Invention III. Means Suitable for Putting the Invention into Effect IV. Knowledge V. Staple Commercial Products VI. Double-territoriality VII. Indirect Infringement of Swiss Form Claims VIII. Indirect Infringement of EPC 2000 Claims IX. Other Forms of Contributory Infringement X. Key Issues for the UPC 5. General Defences I. The Diverse Sources of Defence to Infringement II. The Experimental Use Exemption III. The Bolar Exemption IV. Other Statutory Defences V. Exhaustion VI. De minimis VII. Public Interest Compulsion and Crown Use VIII. Invalidity and Non-Infringement of Claims Asserted IX. Issue Estoppel X. FRAND Licence Objection XI. Prior Use (Article 37 CPC 1989) XII. Innocent Infringement as a Defence to Damages XIII. Key Issues for the UPC 6. Declarations I. General Jurisdictional Basis II. Declarations of Non-Infringement III. Declarations that a Patent is Standard Essential IV. Declarations Concerning Validity V. Key Issues for the UPC 7. FRAND I. Standards, SEPs and FRAND II. Guidance at the European Level III. General Principles of National Law IV. Determining the FRAND Rate V. Anti-Suit Injunctions (ASIs) and Anti-Anti-Suit Injunctions (AASIs) VI. Key Issues for the UPC 8. Remedies I. Statutory Basis II. Preliminary Injunctions III. Damages for Unjustified Injunction IV. Protective Letters V. Quia Timet Injunction VI. Final Injunction VII. Springboard Relief VIII. Award of Damages IX. Account of Profits X. Recall, Removing from the Channels of Commerce and Destruction XI. Publication of Judgment XII. Effect of Tested Validity XIII. Substantive Treatment of Costs XIV. Key Issues for the UPC 9. Patentability and Industrial Application I. Statutory Basis II. Industrial Application III. Excluded Subject-matter IV. Exceptions to Patentability V. Methods of Treatment and Diagnostics – Article 53(c) EPC VI. Key Issues for the UPC 10. Novelty I. Statutory Basis II. General Principles of EPO and National Case Law III. Treatment of Disclosure and Enablement IV. Interpreting Patent Claims and the Prior Art for Novelty Purposes V. Made Available to the Public VI. Novelty Over General Disclosures in the Art VII. Priority VIII. Product by Process Claims IX. Second and Subsequent Medical Uses X. Other Forms of Purpose-limited Claims XI. Claim Amendment XII. Key Issues for the UPC 11. Inventive Step I. Statutory Basis II. Date III. Determination of Fact or Law? IV. Technical or Commercial Question? V. The Role of Common General Knowledge VI. Structured Approaches to Inventive Step VII. Motivation Based Approaches VIII. Criticism of Problem-and-Solution IX. Criticism of Motivation-based Tests X. An Alternative Basis for Assessing Inventive Step XI. Mixed Technical and Non-technical Features XII. Combinations of Prior Art Features XIII. Other Factors XIV. Case Comparison (Tadalafil) XV. Key Issues for the UPC 12. Sufficiency I. Statutory Basis II. General Approaches of EPO and National Law III. Principle of General Application V. Forms of Claim VI. Inventive Improvements / Infringements VII. Promised Quality not Enabled and Errors VIII. Deposits of Biological Material IX. Plausibility in the Context of Insufficiency X. Lack of Clarity XI. Key Issues for the UPC 13. Plausibility I. Is There a Statutory Basis? II. Origins of Plausibility in the EPO III. Inventive Step IV. Insufficiency V. Industrial Applicability VI. The Novelty Context VII. Post-dated Evidence and ab-initio Plausibility VIII. The Plausibility Threshold IX. Further Questions X. Key Issues for the UPC 14. Supplementary Protection Certificates I. Statutory Basis II. Certificates for Plant Protection Products III. Conditions for Grant IV. Protected by a Basic Patent in Force V. Marketing Authorisations in the SPC Context VI. Extent of Protection (Article 4 SPC Regulation) VII. Same Rights as Conferred by the Patent (Article 5 SPC Regulation) VIII. Term IX. Medicinal Products for Paediatric Use X. The SPC Manufacturing Waiver XI. Key Issues for the UPC and the Need for Reform 15. Patent Ownership, Dealings and Employee Inventors I. Introduction II. Ownership III. Approaches to Inventor Compensation IV. Rights of Co-owners V. Patent Dealings VI. Effect of Transfer of Ownership on Licensee VII. Compulsory Licences VIII. Public Interest Compulsion IX. Unitary Patents as 'Objects of Property' 16. Cross-border Actions in Europe I. Relation between National and EPO Proceedings II. The Brussels Regulation IV. Cross-border Infringement Actions VI. Key Issues for the UPC V. Cross-border Declarations of Non-infringement 17. Evidence I. General Principles II. Burden of Proof III. General Obligations to Produce Evidence IV. Specific Means for Obtaining Evidence V. Role of Witness of Fact Evidence VI. Opinion Evidence VII. Experiments VIII. Letters Rogatory (Letters of Request) and US 1782 IX. Border Seizures X. Confidentiality XI. Privilege XII. Key Issues for the UPC Index