At Last a European Patent Court Within Reach
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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be granted in all fields of convention (EPC 1973), which dates back to technology as long as they are new, 1973, was outdated due to a number of comprise an inventive step and are developments in international law and the susceptible of industrial application.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. -
The Public Interest and the Construction of Exceptions to Patentee's Rights
The Public Interest and the Construction of Exceptions to Patentee's Rights - A comparative Study of UK and German law by Marc Dominic Mimler A Thesis Submitted for the Degree of Doctor of Philosophy Queen Mary, University of London 2015 Statement of Originality I, Marc Dominic Mimler, confirm that the research included within this thesis is my own work or that where it has been carried out in collaboration with, or supported by others, that this is duly acknowledged below and my contribution indicated. I attest that I have exercised reasonable care to ensure that the work is original, and does not to the best of my knowledge break any UK law, infringe any third party’s copyright or other Intellectual Property Right, or contain any confidential material. I accept that the College has the right to use plagiarism detection software to check the electronic version of the thesis. I confirm that this thesis has not been previously submitted for the award of a degree by this or any other university. The copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author. Signature: Marc Dominic Mimler Date: 28 May 2015 2 Abstract The thesis analyses the concept of public interest with regards to exceptions to patent rights. It is submitted that patent rights are generally provided for a utilitarian purpose which is to enable technological advance. This goal is meant to be achieved by providing exclusive rights over the patented invention. -
Attachment 1 DECLARATION of JOSEPH STRAUS in Support Re: 61
Doc. 173 Att. 1 Association For Molecular Pathology et al v. United States Patent and Trademark Office et al Dockets.Justia.com C. V. Joseph Straus (Dr. jur, Dres. jur. h.c.), Professor of Law (Universities of Munich and Ljubljana); Marshall B. Coyne Visiting Professor of International and Comparative Law, George Washington University Law School, Washington D.C.; Honorary Director of the Intellectual Property Institute of the Tongji University, Shanghai, Honorary Professor Tongji University, Shanghai; Honorary Professor Huazhong University for Science and Technology, Wuhan; Honorary Director of the Chinese- German Institute for Intellectual Property, Huazhong University, Wuhan; Honorary Professor, University of Xiamen; Visiting Professor, Graduate Institute of Intellectual Property, Taipei; Visiting Fellow, Hoover Institution, Stanford University. Director Emeritus of the Max Planck Institute for Intellectual Property, Competition and Tax Law, Munich (2001-2009); Former Chairman, Managing Board of the Munich Intellectual Property Law Center (MIPLC) (2003-2009) Born: 1938 in Trieste, Italy, received Law-Diploma 1962 from University of Ljubljana, Slovenia, and 1968 Dr. jur. (SJD) from University in Munich. Habilitation in 1986 at University of Ljubljana. Private practise from 1968 to 1977, since then with the Max Planck Institute. Nominated Full Professor of Intellectual Property Law, University of Ljubljana (1986-). Visiting Professor of Law, Cornell Law School, Ithaca, N.Y. (between 1989 and 1998); Distinguished Visiting Professor of Law, Faculty of Law, Toronto University (Spring 2005). Author or co-author of more than 300 publications in the field of intellectual property law, especially in the field of the protection of biotechnological inventions. Consultant to OECD, WIPO, UNCTAD, UNIDO, EC-Commission, World Bank, Scientific Services of the German Bundestag (Federal Parliament) and the German Government, as well as the European Parliament, the European Patent Organisation, the Swiss Government and the Swiss Federal Institute for Intellectual Property. -
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: -
Speech Dr. H. P. Kunz-Hallstein
JIPLP / GRUR Seminar, 6 March 2013 Welcome address by Dr. H. P. Kunz-Hallstein, GRUR President Ladies and Gentlemen, Welcome to Munich! It is my great pleasure to open this Celebratory Seminar at the venerable German Patent- and Trademark Office. Under the name Kaiserliches Patentamt – Imperial Patent Office – it started on 1 July 1877 in Berlin to receive and examine patent applications and reopened after the war in Munich on 1 October 1949. Here it continues – since 1 January 2009 under the presidency of our host, Mrs Rudloff-Schäffer – to live up to its traditional standards which caused the legendary Josef Kohler to call the Patent Office “Die Hauptkulturstätte dieses großartigen Rechtsgebiets” – “The principal cultural site of this great field of law”. Dear Mrs Rudloff-Schäffer, we are very grateful for your hospitality. Our personal acquaintance goes back to the time when we both were working at today’s Max-Planck Institute for Intellectual Property and Competition Law. The good and trusting relations between our Association and you grew up when you decided to work for the Ministry of Justice in Bonn and later in Berlin where you held important responsibilities in the field of intellectual property law. Thank you also for honouring us with your presence and for addressing us. You share the interest and support to the development of European patent law with your predecessors amongst which, to name but one, the unforgotten Kurt Haertel, who went into history as a father of the European Patent Convention. We are also very honoured to have with us a high representative of the European Patent Office which has become – if I may say so – another “principal cultural site of patent law” in this country and which acts just next door; the EPO that examines and grants with great success since 1 June 1978 the European Patents and which will also issue the future European Patents with unitary effect that we will discuss today. -
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. -
International Patent Cooperation Union (Pct Union)
E PCT/A/I/14 ORIGINAL: English WIPO DATE: April 14, 1978 WORLD INTELLECTUAL PROPERTY ORGANIZATION GENEVA INTERNATIONAL PATENT COOPERATION UNION (PCT UNION) ASSEMBLY First Session (1st Extraordinary) Geneva, April 10 to 14, 1978 REPORT Adopted by the Assembly INTRODUCTION 1. The Assembly of the International Patent Cooperation (PCT) Union (hereinafter referred to as “the Assembly”) held its first (extraordinary) session in Geneva from April 10 to 14, 1978. 2. Up to the date of the opening of the session, 18 States (hereinafter referred to as “member States”) had deposited their instruments of ratification of, or accession to, the PCT with the Director General of WIPO. The following 12 member States were represented at the session: Brazil, Cameroon, France, Germany (Federal Republic of), Luxembourg, Madagascar, Senegal, Soviet Union, Sweden, Switzerland, United Kingdom and United States of America. The following six member States were not represented at the session: Central African Empire, Chad, Congo, Gabon, Malawi and Togo. 3. Pursuant to the decision referred to in paragraph 33 below, the following 12 States participated in the session as special observers: Australia, Austria, Canada, Denmark, Finland, Hungary, Ireland, Japan, Netherlands, Norway, Romania and Spain, whereas the following five States were represented by observers: Algeria, German Democratic Republic, Italy, Portugal, and Uruguay. 4. Pursuant to the said decision, two intergovernmental organizations, the European Patent Organisation and the African Intellectual Property -
The Unitary Patent Package Court Competence and Substantive Law
FACULTY OF LAW Lund University Jonas Lembke JAEM03 Master Thesis The unitary patent package Court competence and substantive law European Business Law 30 higher education credits 28 May 2014 Supervisor: Prof. Michael Bogdan Terms: unified patent court; unitary patent; private international law; European patent law 1 Contents ABBREVIATIONS 4 ABSTRACT 6 ACKNOWLEDGEMENT 8 1 INTRODUCTION 9 1.1 Definitions 12 1.2 Brief history of the creation of a Community patent 13 1.2.1 Early days 14 1.2.2 The creation of a Community Patent 15 2 POST MILLENNIA DEVELOPMENT 18 2.1 The London agreement 18 2.2 Community patent continued 19 2.3 C-274/11 and C-295/11 - Spain and Italy v Council 20 2.4 C-146-7/13 Spain v Council 22 2.4.1 Judicial review 24 2.4.2 Legal base for UPR 25 2.4.3 Legal base for UPRL and the language regime 27 2.4.4 Discrimination on language and legal certainty 28 2.5 Opinon 1/09 and a European and EU Patent Court 32 2.6 Current state of affairs 34 3 THE CONTENT OF THE UNITARY PATENT 36 3.1 Regulation (EU) 1257/2012 36 3.1.1 Effects on national law 40 3.2 EPO Rules (draft) 41 4 THE UNIFIED COURT’S JURISDICTION 42 4.1 Brussels I 43 2 4.2 Brussels I amendment consernign UPC 47 4.3 Internal division of competences 49 4.4 Relationship with EPO opposition 50 5 DESIGNATION OF LAW & SUBSTANTIVE LAW 51 5.1 Union law 52 5.1.1 Rome I and Rome II 52 5.1.2 IPRED 55 5.1.3 Supplementary Protection Certificates 55 5.2 Substantive law in UPCA 56 5.2.1 Principles expressed in UPCA 56 5.2.2 Rights conferred and limitations 56 5.2.3 Rules of Procedures -
Examination Guidelines for Patent Applications Relating to Medical Inventions in the Intellectual Property Office
Examination Guidelines for Patent Applications relating to Medical Inventions in the Intellectual Property Office April 2016 © Crown copyright 2016 Intellectual Property Office is an operating name of the Patent Office April 2016 3 Contents Introduction ......................................................................................................................paragraphs 1-5 Basic principles .............................................................................................................paragraphs 6-10 Methods of treatment or diagnosis ...........................................................................paragraphs 11-15 Therapy Definition of “therapy” ....................................................................................................paragraphs 16-17 Therapeutic methods: form of claims ............................................................................paragraphs 18-19 Guidelines for determining whether a method is “treatment by therapy” .....................paragraphs 20-22 Claims to both therapeutic and non-therapeutic methods ...........................................paragraphs 23-28 Therapeutic and non-therapeutic methods: specific examples i) Cosmetic treatments ................................................................................................. paragraph 29 ii) Removal of parasites .........................................................................................paragraphs 30-31 iii) Oral care ................................................................................................................. -
Supreme Court of the United States ------ ------SEQUENOM, INC., Petitioner, V
No. 15-1182 ================================================================ In The Supreme Court of the United States --------------------------------- --------------------------------- SEQUENOM, INC., Petitioner, v. ARIOSA DIAGNOSTICS, INC., et al., Respondents. --------------------------------- --------------------------------- On Petition For A Writ Of Certiorari To The United States Court Of Appeals For The Federal Circuit --------------------------------- --------------------------------- BRIEF OF PROFESSOR TIMO MINSSEN AND ROBERT M. SCHWARTZ WITH 10 EUROPEAN AND AUSTRALIAN LAW PROFESSORS AS AMICI CURIAE IN SUPPORT OF PETITIONER --------------------------------- --------------------------------- ANDREW J. DHUEY Counsel of Record 456 Boynton Avenue Berkeley, CA 94707 (510) 528-8200 [email protected] Counsel for Amici Curiae TIMO MINSSEN Professor of Biotechnology Law (fr. 1 May 2016) FACULTY OF LAW UNIVERSITY OF COPENHAGEN Studiestraede 6 DK-1455 Copenhagen K, Denmark ROBERT M. SCHWARTZ Researcher FACULTY OF LAW LUND UNIVERSITY Lilla Gråbrödersgatan 4 222 22 Lund, Sweden ================================================================ COCKLE LEGAL BRIEFS (800) 225-6964 WWW.COCKLELEGALBRIEFS.COM i TABLE OF CONTENTS Page TABLE OF AUTHORITIES ................................... ii INTEREST OF THE AMICI CURIAE ................... 1 SUMMARY OF ARGUMENT ................................ 2 ARGUMENT ........................................................... 3 I. The European legal framework for patent eligibility ..................................................... -
EPC 2000 the Revised European Patent Convention + the London Agreement
EPC 2000 The Revised European Patent Convention + The London Agreement 2nd edition Königstraße 70 Am Literaturhaus 90402 Nürnberg Telefon: (0911) 89138-0 Telefax: (0911) 89138-29 Am Stein 12 D-97080 Würzburg Telefon: (0931) 286410 Telefax: (0931) 282597 E-Mail: [email protected] Internet: www.ip-goetz.eu 1 What is the EPC? A multilateral treaty (34 contracting states) for a centralised patent grant procedure before a single patent office (EPO). To modernize the European patent system and adapt it to TRIPS (Agreement on Trade Related Aspects of Intellectual Property Rights) and PLT (Patent Law Treaty), the revised EPC 2000 has entered into force on 12/13/2007. 2 What is the London Agreement? A multilateral sub-treaty (14 contracting states) to the EPC for the purpose to save translation costs (see at the end). 3 EPC 2000: Highlights at first glance (I) Changes in substantive patent law ➔ inventions in „all fields of technology“ (adaptation to TRIPS) no substantial change of current practise ➔ use-limited product protection for a second or further medical use of a kown substance (see example below) ➔ novelty-destroying effect of subsequently published EP application having an earlier priority date independent of country designation (see examples below) ➔ strengthening of extent of protection (see below) 4 EPC 2000: Highlights at first glance (II) Procedural „innovations“: ➔ Drastically decreasing requirements for the filing date (adaptation to PLT – see below) ➔ Re-establishment of rights and corrections in respect of priority claim ➔ Further processing of an application as standard legal remedy in respect of observing time limits ➔ Request by patent owner for centralised limitation or revocation of the EP patent ➔ Introduction of a third instance (Enlarged Board of Appeal) for the case of fundamental procedural defects in appeal proceedings (e.g.