EPC 2000 the Revised European Patent Convention + the London Agreement
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State of Intellectual Property Protection and Enforcement in Armenia
State of intellectual property protection and enforcement in Armenia 2020 Supported by Implemented by Table of contents Foreword ............................................................................................................................................... 4 Acknowledgements ............................................................................................................................... 5 About Editors ......................................................................................................................................... 6 Acronyms and Abbreviations ................................................................................................................ 7 Introduction............................................................................................................................................ 9 Executive summary ............................................................................................................................... 11 Chapter 1 Contribution of IP system and IP protection to economic growth and development .......................................................................................................................................... 13 1.1. Importance of efficient IP system for economic growth and development ............. 13 1.2. Importance of IP protection for national economies ............................................... 15 Chapter 2. Current state of the IP system in Armenia .................................................................. -
The European Patent Convention and the London Agreement
Feature European changes The European Patent Convention and the London Agreement EPC 2000 – why change? By Pierre-André Dubois and Shannon The EPC 1973 came into force in 1977 and Yavorsky, Kirkland & Ellis International LLP revolutionised patent practice. However, in the last 30 years, the patent landscape The European Patent Convention (EPC 2000) changed significantly and it became apparent came into force on 13th December 2007, that there was a real need to overhaul the introducing sweeping changes to the dated legislation. First, the Agreement on European patent system. The new Trade Related Aspects of Intellectual convention governs the granting of European Property Rights (TRIPs) and the Patent Law patents by the European Patent Office (EPO) Treaty (PLT) came into force, and it was and applies throughout the 34 contracting questionable whether the EPC 1973 was in states of the European Patent Organisation line with the provisions of each of these (ie, the 27 EU Member States as well as agreements. As one example, the EPC 2000 Croatia, Iceland, Liechtenstein, Monaco, clarifies that, in accordance with TRIPs, Norway, Switzerland and Turkey). The original patents can now be granted in all fields of convention (EPC 1973), which dates back to technology as long as they are new, 1973, was outdated due to a number of comprise an inventive step and are developments in international law and the susceptible of industrial application. Second, need to improve the procedure before the the EPC 1973 was difficult to amend and, in EPO. While the new convention does not the face of fast-changing technology and overhaul substantive patent law (ie, what European legislation, required greater is patentable and what is not), it does legislative flexibility. -
En Munich, 23.11.2018 SUBJECT: Future
CA/99/18 Orig.: en Munich, 23.11.2018 SUBJECT: Future EPO building projects – Orientation paper SUBMITTED BY: President of the European Patent Office ADDRESSEES: Administrative Council (for opinion) SUMMARY This document describes the status of the EPO premises and the related building activities to be further elaborated on in the coming months for a more detailed proposal to the Administrative Council in June 2019. By then the different possible scenarios and their pros and cons will have been evaluated for further decision-making, and initial time schedules and cost estimates for the preferred scenarios will be presented. CA/99/18 e 2018-5337 - I - TABLE OF CONTENTS Subject Page I. STRATEGIC/OPERATIONAL 1 II. RECOMMENDATION 1 III. MAJORITY NEEDED 1 IV. CONTEXT 1 V. ARGUMENTS 3 A. MUNICH 3 B. THE HAGUE 6 C. BERLIN 8 D. VIENNA 8 VI. FINANCIAL IMPLICATIONS 10 VII. DOCUMENTS CITED 10 VIII. RECOMMENDATION FOR PUBLICATION 10 CA/99/18 e 2018-5337 I. STRATEGIC/OPERATIONAL 1. Strategic II. RECOMMENDATION 2. The Council is requested to give an opinion on this orientation paper. III. MAJORITY NEEDED 3. N.A. IV. CONTEXT 4. The President presented the overall strategy for building management and a status review of the EPO premises in his last activities report (CA/88/18). It is stated there that the EPO's building strategy is to deliver a modern working environment along with efficient and effective space management and to preserve the value of the EPO's assets. The Office's main goals for its buildings and the layout of workplaces are: Transparent, flexible and modern workplaces to foster collaboration Similar working conditions for all EPO staff at all sites Working conditions that improve staff well-being Maintenance to preserve asset value Increased sustainability and, in particular, reduction in carbon dioxide footprint Compliance with changing legal requirements to continuously ensure safety and security. -
Working Guidelines Q238 Second Medical Use and Other Second
Working Guidelines by Thierry CALAME, Reporter General Sarah MATHESON and John OSHA, Deputy Reporters General Anne Marie VERSCHUR, Sara ULFSDOTTER and Kazuhiko YOSHIDA Assistants to the Reporter General Q238 Second medical use and other second indication claims Introduction 1) This question seeks to determine the type, scope and enforcement of patent protection for new uses of known chemical compounds when a known substance is found to have a new therapeutic use. For convenience, these guidelines will refer to such use as 'second medical use'. Various types of second medical use are described below. 2) The granting of patent protection for second medical uses potentially provides an important incentive for the identification and development of solutions for unmet medical needs. Second medical use patents can also be a major tool of the originator pharmaceutical industry as part of patent lifecycle management. However, the additional research and development work is time- consuming and expensive. Patent protection is important, but sufficient incentive to encourage research into second medical uses lies in the potential availability of enforceable patent rights of effective scope. 3) Currently, whether patent protection for second medical uses is permitted at all, and if so, the form of permissible claims, varies from country to country. The ability to enforce permissible claims, and the scope of protection afforded, also varies between jurisdictions. Lack of harmonisation impacts both originator and generic pharmaceutical companies by creating uncertainty both for patent holders and assumed infringers. 4) The granting of patent protection for second medical uses gives rise to competing positive and negative impacts on the provision of effective medicines to the public. -
Patent-Related Barriers to Market Entry for Generic Medicines in the European Union
atents play an important role in modern society. In order to encourage the creation, dissemination and efficient P exploitation of technology, patents provide inventors Patent-related Barriers with a limited term legal monopoly on their invention. Generic medicines play an equally important role in promoting to Market Entry for pharmaceutical innovation and ensuring the affordability and sustainability of European healthcare systems. In this regard, Generic Medicines in immediate market access of generic medicines after patent expiry is of crucial interest to society, and any hurdle to this the European Union access should be eliminated. However, a number of developments point to a strategic use of patents—of sometimes questionable quality—which is directed more toward preventing others from innovating and competing, A Review of Weaknesses in the Current than toward creating truly innovative products. When misused European Patent System and their Impact in this manner, patents can present a barrier to entry onto the on the Market Access of Generic Medicines generic medicines market. This report identifies some of the hurdles that generic medicines companies face in this regard in the European Union. Editor Kristof Roox | Attorney at the Brussels Bar | Belgium European Patent Office Headquarters | Munich, Germany EUROPEAN GENERIC MEDICINES ASSOCIATION EUROPEAN GENERIC Rue d’Arlon 50 B-1000 Brussels | Belgium MEDICINES ASSOCIATION Tel: +32 (0) 2 736 84 11 | Fax: +32 (0) 2 736 74 38 www.egagenerics.com | [email protected] Layout & Design: -
Patent Cooperation Treaty (PCT) Working Group
Annex 1 E PCT/WG/11/27 ORIGINAL: ENGLISH DATE: JANUARY 11, 2019 Patent Cooperation Treaty (PCT) Working Group Eleventh Session Geneva, June 18 to 22, 2018 REPORT adopted by the Working Group 1. The Patent Cooperation Treaty Working Group held its eleventh session in Geneva from June 18 to 22, 2018. 2. The following members of the Working Group were represented at the session: (i) the following Member States of the International Patent Cooperation Union (PCT Union): Algeria, Australia, Austria, Belarus, Brazil, Bulgaria, Canada, Chile, China, Colombia, Côte d’Ivoire, Czech Republic, Democratic People’s Republic of Korea, Denmark, Ecuador, Egypt, El Salvador, Finland, France, Georgia, Germany, Greece, Guatemala, Honduras, Hungary, India, Indonesia, Iran (Islamic Republic of), Israel, Italy, Japan, Kazakhstan, Kuwait, Lithuania, Malaysia, Malta, Mexico, Montenegro, Morocco, Nigeria, Norway, Oman, Peru, Philippines, Poland, Portugal, Republic of Korea, Romania, Russian Federation, Saudi Arabia, Senegal, Singapore, Slovakia, South Africa, Spain, Sudan, Sweden, Switzerland, Thailand, Trinidad and Tobago, Turkey, Uganda, Ukraine, United Arab Emirates, United Kingdom, United States of America, Uzbekistan, Viet Nam, Zimbabwe (69); and (ii) the following intergovernmental organizations: the European Patent Office (EPO), the Nordic Patent Institute (NPI), and the Visegrad Patent Institute (VPI) (3). 3. The following Member States of the International Union for the Protection of Industrial Property (Paris Union) participated in the session as an observer: Mauritius, Yemen (2). 4. The following intergovernmental organizations were represented by observers: African Intellectual Property Organization (OAPI), African Regional Intellectual Property Organization (ARIPO), African Union (AU), Eurasian Patent Organization (EAPO), European Union (EU), Patent Office of the Cooperation Council for the Arab States of the Gulf (GCC Patent Office), South Centre (7). -
Patent Harmonisation and Utilisation: First Europe and Then the World?
Patent Harmonisation and Utilisation: First Europe and Then the World? Dr Mark Weaver 3 December 2009 Director Practice & Procedure Utilisation and Harmonisation - Drivers Challenges • Worldwide Patent Application Backlogs - Millions • Duplication of Work • Increased Costs • Lack of Consistency • Increased Legal Uncertainty Possible Solutions • Utilisation and Work Sharing • New Bilateral or Multi-Lateral Agreements • Improve on Existing Work Sharing Agreements • Substantive Patent Law Harmonisation • Simplified Language Requirements First Europe ... European Patent Landscape EPO - 36 Member States Unified Patent Litigation System Austria • Belgium • Bulgaria • Croatia • UPLS Cyprus • Czech Republic • Denmark • Estonia • Finland • France • Germany • Greece • Hungary • Iceland • Ireland • Italy • Latvia • Liechtenstein • Lithuania • Luxembourg • Former Yugoslav Republic of European and Macedonia • Malta • Monaco • Netherlands • Community Norway • Poland • Portugal • Romania • Community San Marino • Slovakia • Slovenia • Spain • Patents Court Patent Sweden • Switzerland • Turkey • United Kingdom ECPC European patent applications and patents can European also be extended at the applicant's request to Enhanced Patent Network the following states: Partnership Albania • Bosnia-Herzegovina • Serbia EPN Status: December 2009 European Patent Landscape • Unified Patent Litigation System • Draft Council Conclusions on an enhanced patent system in Europe http://register.consilium.europa.eu/pdf/en/09/st14/st14040.en09.pdf • Draft Council Agreement -
The European Patent Convention, 3 Md
Maryland Journal of International Law Volume 3 | Issue 2 Article 10 The urE opean Patent Convention Follow this and additional works at: http://digitalcommons.law.umaryland.edu/mjil Part of the International Law Commons, and the International Trade Commons Recommended Citation The European Patent Convention, 3 Md. J. Int'l L. 408 (1978). Available at: http://digitalcommons.law.umaryland.edu/mjil/vol3/iss2/10 This Notes & Comments is brought to you for free and open access by DigitalCommons@UM Carey Law. It has been accepted for inclusion in Maryland Journal of International Law by an authorized administrator of DigitalCommons@UM Carey Law. For more information, please contact [email protected]. THE EUROPEAN PATENT CONVENTION The European Patent Convention' (EPC) is an attempt to simplify European patent law. The Convention provides a procedure for securing a single, European patent,2 which has the effect of a national patent in the signatory nations designated in the application. Through this alternative to national procedures, widespread patent coverage should be easier to obtain. Require- patent, however, are rigorous and its ments for a European 3 attraction is primarily the consolidation of the grant procedures. The EPC establishes several organs to handle the various aspects of the patent application procedure. The European Patent Office (EPO), located in Munich, is the international equivalent of a national patent office. Its administrative divisions are the General Search Division, the Examining Division, and the Opposition Division. The Receiving Section is at The Hague. The first procedural step is the filing of an application at either a national patent office or directly with the EPO.4 The application may be in any of the three official languages (English, French, or German) and the applicant's choice becomes the language of the proceedings.5 The Receiving Section subjects the application to both a preliminary6 and a supplementary formal examination to determine whether it is in proper form and all fees are paid. -
Doing Business in Kazakhstan
DOING BUSINESS 2021 IN KAZAKHSTAN Doing Business in Kazakhstan 2021 Baker McKenzie – CIS, Limited Almaty office Samal Towers, 8th Floor 97 Zholdasbekov Street Almaty, Kazakhstan 050051 Phone: +7 727 3 300 500 Facsimile: +7 727 258 40 00 [email protected] www.bakermckenzie.com The information in this brochure is for informational purposes only and it may not reflect the most current legal developments, judgments or settlements. This information is not offered as legal or any other advice on any particular matter. The Firm and the contributing authors expressly disclaim all liability to any person in respect of anything and in respect of the consequences of anything done or omitted wholly or partly in reliance upon the whole or any part of the contents of Baker McKenzie’s “Doing Business in Kazakhstan” brochure. No client or other reader should act or refrain from acting on the basis of any matter contained in this brochure without seeking the appropriate legal or other professional advice on the particular facts and circumstances. Doing Business in Kazakhstan Table of Contents 1 Kazakhstan — an overview ..................................................... 1 1.1 Geography .................................................................... 1 1.2 Population .................................................................... 1 1.3 History.......................................................................... 1 1.4 Government and political system ................................. 2 1.5 Economy ..................................................................... -
EUROPEAN PATENT OFFICE Guidelines for Examination General Part Amended in December, 2007
EUROPEAN PATENT OFFICE Guidelines for Examination General Part Amended in December, 2007 CONTENTS 1. Preliminary remarks 2. Explanatory notes 2.1 Overview 2.2 Abbreviations 3. General remarks 4. Work at the EPO 5. Survey of the processing of applications and patents at the EPO 6. Contracting States to the EPC 7. Extension to states not party to the EPC 1 1. Preliminary remarks In accordance with Art. 10(2)(a) of the European Patent Convention (EPC), the President of the European Patent Office (EPO) had adopted, effective as at 1 June 1978, the Guidelines for Examination in the European Patent Office. These Guidelines have been and will be updated at regular intervals to take account of developments in European patent law and practice. Amended or new text (as compared to the latest previous version only) is indicated by a vertical line in the right-hand margin. Mere deletions are indicated by two horizontal lines in the right-hand margin. Usually, updates only involve amendments to specific sentences or passages on individual pages, in order to bring at least part of the text more closely into line with patent law and EPO practice as these continue to evolve. It follows that no update can ever claim to be complete. Any indication from readers drawing the attention to errors as well as suggestions for improvement are highly appreciated and may be sent by e-mail to: [email protected] The Guidelines for Examination in the European Patent Office are also published by the EPO in an electronic, searchable form on the Internet via the EPO website: http://www.epo.org 2. -
INTELLECTUAL PROPERTY Patent Cooperation
TREATIES AND OTHER INTERNATIONAL ACTS SERIES 13-1218.1 ________________________________________________________________________ INTELLECTUAL PROPERTY Patent Cooperation Treaty Between the UNITED STATES OF AMERICA and OTHER GOVERNMENTS Adopted at Geneva June 1, 2000 with Amended Schedule Adopted May 15, 2008 NOTE BY THE DEPARTMENT OF STATE Pursuant to Public Law 89—497, approved July 8, 1966 (80 Stat. 271; 1 U.S.C. 113)— “. .the Treaties and Other International Acts Series issued under the authority of the Secretary of State shall be competent evidence . of the treaties, international agreements other than treaties, and proclamations by the President of such treaties and international agreements other than treaties, as the case may be, therein contained, in all the courts of law and equity and of maritime jurisdiction, and in all the tribunals and public offices of the United States, and of the several States, without any further proof or authentication thereof.” MULTILATERAL Intellectual Property: Patent Cooperation Treaty adopted at Geneva June 1, 2000; Transmitted by the President of the United States of America to the Senate September 5, 2006 (Treaty Doc. 109-12, 109th Congress, 2d Session); Reported favorably by the Senate Committee on Foreign Relations September 11, 2007 (Senate Executive Report No. 110-6, 110th Congress, 1st Session); Advice and consent to ratification by the Senate December 7, 2007; Ratified by the President May 6, 2008; Ratification deposited September 18, 2013; Entered into force December 18, 2013. With Amended Schedule adopted May 15, 2008. PATENT LAw TREATY (PLT) PATENT LAW TREATY (PLT) and REGULATIONS UNDER THE PATENT LAW TREATY Done at Geneva on June 1, 2000 and EXPLANATORY NOTES ON THE PATENT LAW TREATY and THE REGULATIONS UNDER THE PATENT LAW TREATY 2 NOTE: This page appears to be intentionally blank, except for page number. -
WEICKMANN & WEICKMANN LONDON Agreement Overview
1 YEARS 2 WEICKMANN & WEICKMANN 8 0 8 0 125JAHRE Patentanwälte 2 7 European Patent Attorneys · European Trademark and Design Attorneys DIPL.-ING. H. WEICKMANN (bis 2001) DIPL.-ING. F. A. WEICKMANN DIPL.-CHEM. B. HUBER (bis 2006) DR.-ING. H. LISKA DIPL.-PHYS. DR. J. PRECHTEL LL.M. DIPL.-CHEM. DR. B. BÖHM DIPL.-CHEM. DR. W. WEISS DIPL.-PHYS. DR. J. TIESMEYER DIPL.-PHYS. DR. M. HERZOG DIPL.-PHYS. B. RUTTENSPERGER DIPL.-PHYS. DR.-ING. V. JORDAN DIPL.-CHEM. DR. M. DEY DIPL.-FORSTW. DR. J. LACHNIT Newsletter LL.M. DR. U. W. HERBERTH * DR.-ING. H.-J. TROSSIN 2008/03 * Rechtsanwalt LONDON Agreement Overview Our last newsletter (2008/02) generally informed about the London Agreement. Now further details of the translation requirements have become known. To give you an overview of the present situation, we enclose a map of the member states of the European patent organisation and a corresponding table indicating the states which are members of the LONDON Agreement (green, blue, blue hatched) and the states which are not yet member states of the LONDON Agreement (yellow). States marked green are those member states of the LONDON Agreement which do not require a translation. States marked blue are those member states of the LONDON Agreement which require a translation of the claims into the national language. States marked blue hatched are those member states of the LONDON Agreement which not only require the claims to be translated into the national language but also require the filing of an English translation of the specification if the patent specification is not written in English.