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Chapter 1 Eligibility for Patent and Industrial Applicability (Main Paragraph of Article 29(1) of the Patent Act)
Note: When any ambiguity of interpretation is found in this provisional translation, the Japanese text shall prevail. Part III Chapter 1 Eligibility for Patent and Industrial Applicability Chapter 1 Eligibility for Patent and Industrial Applicability (Main Paragraph of Article 29(1) of the Patent Act) 1. Overview The main paragraph of Article 29(1) of the Patent Act defines that any person who has made an invention which is industrially applicable may obtain a patent therefor. Article 2(1) of the Patent Act defines "invention" as "the highly advanced creation of technical ideas utilizing the laws of nature". An invention which does not comply with this definition shall not be patented. An invention for which a patent is sought shall be industrially applicable even if the patent complies with this definition, since the purpose of the Patent Act is the development of industry (Article 1). The main paragraph of Article 29(1) of the Patent Act provides the two following points as the patentability requirements: (i) A statutory "invention" (hereinafter, referred to as "eligibility for a patent" in this chapter) (see 2.) (ii) An "industrially applicable invention" (hereinafter, referred to as "industrial applicability" in this chapter) (see 3.) This chapter explains determination on eligibility for a patent and industrial applicability. In this chapter, an invention complying with the requirements of eligibility for a patent is referred to as a statutory "invention". The word "invention" in the expression "claimed invention" does not mean that the invention complies with the requirements of eligibility for a patent. 2. Determination on Requirements of Eligibility for Patent The subject of determination on the requirements of eligibility for a patent is a claimed invention. -
The Success Of, and Response To, India's Law Against Patent Layering
The Success of, and Response to, India’s Law against Patent Layering Rajarshi Banerjee. J.D. Candidate, Harvard Law School, 2014 I. INTRODUCTION ...................................................................................................... 2 II. THE DEBATE OVER PATENT LAYERING ...................................................... 5 A. An Introduction to Patent Layering ........................................................................ 5 B. Arguments for and against Patent Layering ........................................................... 6 III. THE GLOBAL PATENT PROTECTION LANDSCAPE ..................................... 9 A. The Emergence of TRIPS ........................................................................................ 9 B. Patent Protection under the International Investment Regime ............................. 12 C. Patent Protection under Other Agreements that Implicate Intellectual Property 15 D. Most-Favored-Nation Provisions in TRIPS and International Investment Agreements (IIAs) ......................................................................................................... 16 IV. THE CHALLENGE OF LIMITING PATENT LAYERING AMIDST THE GLOBAL PATENT PROTECTION LANDSCAPE ........................................................ 16 V. THE SUCCESS OF INDIA’S LAW AGAINST PATENT LAYERING ............ 17 A. An Introduction to India’s Law against Patent Layering ..................................... 18 B. How India’s Law Interacts with the Global Patent Protection Landscape .......... 21 1. Section -
Overview of the Patent System and Procedure in Sri Lanka
Overview of the Patent System and Procedure in Sri Lanka Outline n What is intellectual property? n Types of intellectual property n Evolution of the domestic system n International Arena n Why do intellectual property rights matter? n Patent system n Patenting Procedure n Patent CooperationTreaty 2 What is Intellectual Property (IP)? n IP is the term used for types of property that result from creations of human mind, the intellect. n IP is an asset and has a monetary value. n IP can be owned, transferred, sold or licensed. n A kind of intangible property and has no physical form. n IP is divided into two general categories n Industrial Property n Copyrights 3 Types of Intellectual Property n Industrial Property – assets created for the advancement of technology, industry and trade. n Patents n Trademarks n Industrial Designs n Geographical Indications n Copyrights and related rights – original expressions and “work of authorship” 4 Evolution of the domestic system n The first patent was granted on November 22, 1860 in Sri Lanka under the British Inventor’s Ordinance of 1859. n The Patents Ordinance of 1906 (based on the English Patent Law). n The English Law of Trademarks in 1888 under the Ordinance No. 14 of 1888. n The Design Ordinance in 1904. n The Copyright Ordinance No 12 of 1908 is the first copyright law in Sri Lanka. 5 Evolution of the domestic system n The Code of Intellectual Property Act N0.52 of 1979 – turning point in the evolution of IP law and administration in Sri Lanka. n New regime – The Intellectual Property Act, N0.36 of 2003 which provides the law relating to IP and for an efficient procedure for registration, control and administration. -
Software Patent Law: United States and Europe Compared
SOFTWARE PATENT LAW: UNITED STATES AND EUROPE COMPARED Software is a global business. Patents are increasingly the protection of choice; as a consequence, international software patent laws are of growing importance to software vendors. This article focuses on European patent law and how it differs from United States law in regards to software technology. Statutes and relevant case law of both unions are discussed and compared, providing an introductory secondary source for scholars and practitioners. Introduction In the past, industrial countries had their own patent laws and offices. Those seeking protection in a specific country had to apply for a national patent and obey local laws. With increasing globalization, international agreements were made and organizations founded to reconcile regional differences: The 1883 Paris Convention1 was based on the principle of reciprocal national treatment and therefore dealt more with international comity than the unification of patent laws. The 1970 Patent Cooperation Treaty (PCT)2 finally implemented international one-stop patents.3 Both treaties are administered by the World Intellectual Property Organization (WIPO).4 1 The Paris Convention for the Protection of Intellectual Property was enacted on March 20, 1883. It has been amended most recently in 1970. http://www.wipo.int/clea/docs/en/wo/wo020en.htm. 2 The Patent Cooperation Treaty (PCT) was adopted on June 19, 1970 in Washington, D.C., and has been encoded in 35 U.S.C. §§ 351-76 (2000). 28 U.S.T. 7645. It has been modified most recently in October 2001. http://www.wipo.org/pct/en/index.html. 3 International one-stop patents—generally called PCTs after the enabling treaty—are patents that are recognized by all WIPO member countries (see n.4, infra). -
Outline of the Examination Guidelines for Patent and Utility Model
Outline of the Examination Guidelines for Patent and Utility Model Examination Standards Office Japan Patent Office 2018.06 Flow of examination on patent applications (outline) Supreme Court Intellectual Property High Court If the reasons for refusal are not solved Appeal If there are new reasons for refusal Submission of written opinion/amendment Decision of refusal If there are reasons for refusal Notification of reasons If there are no for refusal reasons for refusal Substantive examination Decision to grant a patent Registration to establish patent If there are no reasons for refusal Request for examination Patent gazette Within 3 years Application is filed 18 months Publication for a patent 1 1. Introduction of the Examination Guidelines 2. Novelty and Inventive Step 3. Secret Prior Art 4. Double Patenting 5. Requirements for Description and Claims 6. Unity of Invention 7. Industrially Applicable Inventions (Patentable Subject Matter) 8. Amendment 9. Overview of the March 2016 revision 2 1. Introduction of the Examination Guidelines 2. Novelty and Inventive Step 3. Secret Prior Art 4. Double Patenting 5. Requirements for Description and Claims 6. Unity of Invention 7. Industrially Applicable Inventions (Patentable Subject Matter) 8. Amendment 9. Overview of the March 2016 revision 3 1. Introduction of Examination Guidelines The Examination Guidelines summarize, so as to ensure fairness and transparency, Basic ideas of when applying laws such as applying the regulations in the Patent Act to patent examinations Criteria for Indicator for examinations managing patents Examination Guidelines are available at JPO’s website: https://www.jpo.go.jp/e/system/laws/rule/guideline/patent/tukujitu_kijun/index.html 4 1. -
Section a Patents, Utility Models and Microorganisms
SECTION A PATENTS, UTILITY MODELS AND MICROORGANISMS SECTION A PATENTS, UTILITY MODELS AND MICROORGANISMS Over the past two decades, the patent system has The Patent System undergone important changes worldwide. As a result, patent legislation and patenting behavior have become A patent confers, by law, a set of exclusive rights to ap- prominent public policy themes. Similarly, use of the utility plicants for inventions that meet the standards of novelty, model (UM) system for protecting inventions has risen in non-obviousness and industrial applicability. It is valid for certain countries. a limited period of time (generally 20 years), during which patent holders can commercially exploit their inventions This section provides an overview of patent and UM activ- on an exclusive basis. In return, applicants are obliged ity worldwide to enable users to analyze and monitor the to disclose their inventions to the public so that others, latest trends. It presents a wide range of indicators that skilled in the art, may replicate them. The patent system offer insights into the functioning and use of the patent is designed to encourage innovation by providing innova- and UM systems. tors with time-limited exclusive legal rights, thus enabling them to appropriate the returns of their innovative activity. Disclosure of an invention is a generally recognized requirement for the granting of a patent. Where an in- The procedures for acquiring patent rights are governed vention involves microorganisms, national laws in most by the rules and regulations of national and regional countries require that the applicant deposit a sample at a patent offices. These offices are responsible for issuing designated International Depositary Authority (IDA). -
Evergreening – a Controversial Issue in Pharma Milieu*
Journal of Intellectual Property Rights Vol 14, July 2009, pp 299-306 Evergreening – A Controversial Issue in Pharma Milieu* Inderjit Singh Bansal, Deeptymaya Sahu, Gautam Bakshi and Sukhjeet Singh† Panacea Biotec Ltd, Formulation & Research Facility, Sampann R&D, Ambala - Chandigarh Highway, Lalru, Punjab 140 501 Received 18 March 2009, revised 22 June 2009 A patent is an exclusive right awarded by the intellectual property (IP) authority of a state to an inventor or his assignee for a limited period of time in lieu of disclosure of an invention for the benefit of mankind. In recent times, it has become a practice by a number of innovator companies to extend the patent term of their innovative molecules to maintain market dominance. The extension of monopoly term ‘Evergreening’ is a predominant aspect of pharmaceutical patenting. ‘Evergreening’ refers to different ways wherein patent owners take undue advantage of the law and associated regulatory processes to extend their IP monopoly particularly over highly lucrative ‘blockbuster’ drugs by filing disguised/artful patents on an already patent-protected invention shortly before expiry of the ‘parent’ patent. These artful patents tend to protect delivery profiles, packaging, derivatives, and isomeric forms, mechanism of action, dosing regimen, and dosing range, and dosing route, different methods of treatment, combinations, screening methods, biological targets and field of use for the same old molecule. This provides the innovator companies sufficient time to recoup their controversially estimated R&D costs. Patent monopolies thus should be designed to function at an optimum level wherein maximum incentive is accorded to investment in research followed by simultaneous accessibility of the protected inventions to the public. -
Is Intellectual Property Important for Future Manufacturing Activities?
Is intellectual property important for future manufacturing activities? Future of Manufacturing Project: Evidence Paper 12 Foresight, Government Office for Science Is intellectual property important for future manufacturing activities? By Professor Bronwyn H. Hall University of California October 2013 This review has been commissioned as part of the UK Government’s Foresight Future of Manufacturing Project. The views expressed do not represent policy of any government or organisation. Contents Executive summary...................................................................................................................... 4 1. Introduction............................................................................................................................... 5 2. Trends in manufacturing and investment .............................................................................. 6 2.1 Intangible investment in manufacturing .................................................................................. 6 2.2 Trends in R&D investment ...................................................................................................... 8 3. Worldwide trends in intellectual property use..................................................................... 11 3.1 Growth in IP use ................................................................................................................... 11 4. IP and intangible assets in UK manufacturing .................................................................... 17 4.1 Current -
Legal Requirements for Patentability and Typical Parts of a Patent Application
Topic 3: Legal Requirements for Patentability and typical Parts of a Patent Chiang Mai, Application October 2, 2017 Atif W. Bhatti Associate Legal Officer, Patent Law Section, WIPO 2 Overview National Law Exceptions to Patentability Novelty Inventive Step Industrial Applicability 3 National Law Thai Patent Act (1979) Sec. 5 : „new, involve an inventive step and capable of industrial application “ Sec. 6, 7 and 8: further definitions for novelty, inventive step and industrial applicability Sec. 9: exclusions to patentability 4 Exceptions to Patentability Depends on national or regional law! Discovery, Scientific theories, mathematical methods Aesthetic creations Inventions contrary to morality or public order Therapeutic and diagnostic methods Plant or animal varieties Plants or animals (other than microorganisms) 5 Exceptions to Patentability Software! However, software implemented inventions might be patentable i.e. invention involving an apparatus or process which makes use of a software, e.g. a specific computer chip with a software stored on it 6 Novelty An invention is new/novel if it was not know to the public before the date of filing of the patent application or the priority date claimed. Prior art should not be patented again! 7 Novelty Absolute Novelty No publication of the invention anywhere in the world by means of written or oral description, by use, or in any other way Also know as strict novelty requirement Each feature of the invention in general in one single reference 8 Novelty Some national laws have a grace period e.g. USA, Japan, etc. But not European countries! Making available to the public within certain period before the date of filing not novelty destroying (e.g. -
Guidelines for the Examination of Patent Applications Relating to Pharmaceuticals Cover Photo: Sami Siva
Empowered lives. Resilient nations. United Nations Development Programme Guidelines for the examination of patent applications relating to pharmaceuticals Cover photo: Sami Siva Document design and layout: P D Design Guidelines for Pharmaceutical Patent Examination: Examining Pharmaceutical Patents from a Public Health Perspective Carlos M Correa Empowered lives. Resilient nations. GUIDELINES FOR PHARMACEUTICAL PATENT EXAMINATION: EXAMINING PHARMACEUTICAL PATENTS FROM A PUBLIC HEALTH PERSPECTIVE 1 Acronyms and Abbreviations 5ASA 5-aminosalicylic acid 5-FU 5-fluorouracil AIDS Acquired immune deficiency syndrome AZT Zidovudine DAT Dementia of the Alzheimer type DCL Descarboethoxyloratadine EPO European Patent Office HIV Human immunodeficiency virus ICTSD International Centre for Trade and Sustainable Development IR Infrared absorption spectrum NIF Neutrophil inhibitory factor NMDA N-methyl-D-aspartate NMR Nuclear magnetic resonance NOS Nitric oxide synthase NRTIs Nucleotide analogue reverse transcriptase inhibitors R&D Research & Development SDG Sustainable Development Goal TRIPS Trade-related Aspects of Intellectual Property Rights UNCTAD United Nations Conference on Trade and Development UNDP United Nations Development Programme USPTO US Patent and Trademark Office WHO World Health Organization WTO World Trade Organization 2 GUIDELINES FOR PHARMACEUTICAL PATENT EXAMINATION: EXAMINING PHARMACEUTICAL PATENTS FROM A PUBLIC HEALTH PERSPECTIVE Contents Acronymns and Abbreviations 2 Acknowledgements 4 Foreword 5 Executive summary 6 Summary -
Japanese Patent Law and the WIPO Patent Law Harmonization Treaty: a Comparative Analysis
Fordham Intellectual Property, Media and Entertainment Law Journal Volume 4 Volume IV Number 3 Volume IV Book 3 Article 5 1994 Japanese Patent Law and the WIPO Patent Law Harmonization Treaty: A Comparative Analysis Mark S. Cohen Cooper & Dunham Follow this and additional works at: https://ir.lawnet.fordham.edu/iplj Part of the Entertainment, Arts, and Sports Law Commons, and the Intellectual Property Law Commons Recommended Citation Mark S. Cohen, Japanese Patent Law and the WIPO Patent Law Harmonization Treaty: A Comparative Analysis, 4 Fordham Intell. Prop. Media & Ent. L.J. 847 (1994). Available at: https://ir.lawnet.fordham.edu/iplj/vol4/iss3/5 This Article is brought to you for free and open access by FLASH: The Fordham Law Archive of Scholarship and History. It has been accepted for inclusion in Fordham Intellectual Property, Media and Entertainment Law Journal by an authorized editor of FLASH: The Fordham Law Archive of Scholarship and History. For more information, please contact [email protected]. Japanese Patent Law and the WIPO Patent Law Harmonization Treaty: A Comparative Analysis Cover Page Footnote The author is grateful for the guidance and support of William T. Fryer, III, Professor of Law, University of Baltimore School of Law, Baltimore, Md. The author also wishes to acknowledge Yoichiro Yamaguchi, Esq., Beveridge, DeGrandi, Weilacher & Young, Washington, D.C., for his comments on this Article. This article is available in Fordham Intellectual Property, Media and Entertainment Law Journal: https://ir.lawnet.fordham.edu/iplj/vol4/iss3/5 ARTICLE Japanese Patent Law and the WIPO Patent Law Harmonization Treaty: A Comparative Analysis Mark S. -
Patentability Criteria
TRIPS Pre-Grant Flexibilities: Patentability Criteria Christoph Spennemann, Legal Expert IP Unit, Division on Investment and Enterprise UNCTAD UNCTAD/CD-TFT 1 Overview of Presentation • Rights under a granted patent • Patentability criteria under TRIPS • Novelty • Inventive step • Industrial applicability • Ever-greening of patents • New uses of known products • Derivatives of known products UNCTAD/CD-TFT 2 TRIPS Article 27.1 on patentability criteria • Subject matter that • Constitutes an invention (natural substances!) and • is not excluded from patentability (methods of medical treatment) • Such patentable subject matter still needs to meet three criteria: • Novelty • Inventive step (non-obviousness) • Industrial applicability (utility) UNCTAD/CD-TFT 3 Patents: scope • A product (e.g. pharmaceutical) • A way of making the product • A way of using the product • Some combination of the above • TRIPS Article 28.1: • Product patents • Process patents UNCTAD/CD-TFT 4 Product patents • 28.1 (a) TRIPS: Right to prevent third parties not having the owner’s consent from the acts of • making, • using, • offering for sale, • selling, or • importing for these purposes that product (subject to exhaustion of patent rights) UNCTAD/CD-TFT 5 Process patents • 28.1 (b) TRIPS: Right to prevent third parties not having the owner’s consent from • the act of using the process, and • from the acts of: • using, • offering for sale, • selling, or • importing for these purposes at least the product obtained directly by that process. UNCTAD/CD-TFT 6 Difference