Table of Patent Fees - Current, Final Rule and Unit Cost
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Basic Understanding of Intellectual Property
BASIC UNDERSTANDING OF INTELLECTUAL PROPERTY Jacob N. (Jesse) Erlich, Partner, Burns & Levinson LLP Kathy Chapman, Assistant Counsel IP, U.S. Naval Research Laboratory BACKROUND A company or individual entering the world of business should maintain ownership of its innovative developments. These innovative developments generally take the form of intellectual property, which is broadly defined as protectable developments of the mind. A more formal definition of intellectual property is an intangible or proprietary asset such as a patent, copyright, trademark, or trade secret. To better understand the various aspects of intellectual property protection, it is best to first understand that most intellectual property, particularly inventions, begins as a trade secret. Although patents may be the most common and well-known form of intellectual property, at its outset all forms of intellectual property begin as a trade secret. A trade secret is used to protect important business information that a business or an individual does not want to disclose to the public. In other words, to rely on trade secret protection, one must ensure that such trade secrets remain confidential. As a business develops, it becomes increasingly difficult to keep such information confidential; as such, the chances are that this information will become released to the public and protection will be lost. Therefore, it is important to understand various other types of intellectual property protection such as patents, trademarks, and copyrights. TRADE SECRETS The use of trade secrets to protect one's ideas is extremely important and can be considered an essential part of a business. However, to use trade secrets as a form of intellectual property protection, trade secrets must be kept confidential. -
Effects of Supplementary Protection Mechanisms for Pharmaceutical Products
Final report, May 2018 Effects of supplementary protection mechanisms for pharmaceutical products www.technopolis-group.com Effects of supplementary protection mechanisms for pharmaceutical products technopolis |group| May 2018 Thyra de Jongh* Alfred Radauer Sven Bostyn Joost Poort * Corresponding author. [email protected] About the authors Thyra de Jongh PhD, is a Senior Consultant Health & Life Sciences at Technopolis Group in Amsterdam. She specialises in analysis of health systems and policies, and research and innovation in the health and life sciences. She has a particular interest in pharmaceutical innovation and access to medicine. (thyra.dejongh@technopolis- group.com) Alfred Radauer, is Senior Consultant at Technopolis Group in Vienna and leads the Intellectual Property & Standards (IPS) group within Technopolis. His and the IPS group work elaborate on the interfaces between legal, technological and economic issues of IP and standards in innovation policy as well as the interaction of IP with regulation and other policy areas. ([email protected]) Sven Bostyn Lic.Jur, LL.M, PhD, is a senior lecturer in Intellectual Property Law at the University of Liverpool Law School. He is also an assistant professor at the Institute for Information Law, University of Amsterdam. He is one of the leading experts in Europe in patent law and related subjects in the areas of life sciences and pharmaceutical inventions, and has more than sixty single-authored publications. ([email protected]) Joost Poort PhD, is an associate professor in economics at the Institute for Information law, University of Amsterdam. He brings an economic perspective to various multidisciplinary research projects, with particular interest in intellectual property. -
US Patent Basics
US Patent Basics *A free e-copy of this book is available by request to [email protected]. US Patent Basics By Tamsen Valoir, PhD. Tamsen is a partner in the Houston office of Boulware & Valoir. She has a JD and LLM in Intellectual Property, a doctorate in molecular biology from Rice University, and her practice is primarily in intellectual property in the area of life sciences. [email protected]. 7th Edition, © 2012. Table of Contents 1. US PATENT BASICS ................................................................... 2 2. BEST MODE, OATH, CANDOR .................................................. 15 3. INVENTORSHIP ....................................................................... 18 4. PATENT REFORM 2011 ........................................................... 21 5. COST CONTROL ..................................................................... 29 6. PATENT STRATEGY ................................................................. 32 7. INTERNATIONAL PROTECTION ................................................ 38 8. RECEIPT OF A US PATENT ....................................................... 41 9. PATENT ENFORCEMENT .......................................................... 44 10. OTHER TYPES OF PROTECTION .............................................. 46 11. FDA BASICS .......................................................................... 49 12. TEN ISSUES FOR THE START-UP ............................................ 54 13. PATENT STATUTES ............................................................... -
ACT No. 173/2002 Coll. of 9 April 2002 on Fees for Maintenance of Patents and Supplementary Protection Certificates for Medicame
ACT No. 173/2002 Coll. of 9 April 2002 on Fees for Maintenance of Patents and Supplementary Protection Certificates for Medicaments and Plant Protection Products and on Amendment of some Acts PART ONE FEES FOR MAINTENANCE OF PATENTS AND SUPPLEMENTARY PROTECTION CERTIFICATES FOR MEDICAMENTS AND FOR PLANT PROTECTION PRODUCTS Section 1 Subject matter of regulation (1) This Act shall regulate assessment and collection of fees for maintenance of a patent in force (“maintenance fees for a patent”), fees for maintenance of a European patent with effects for the Czech Republic in force (“maintenance fees for a European patent”), fees for maintenance of a supplementary protection certificate for medicaments and for plant protection products in force (“maintenance fees for supplementary certificates”).1 (2) Fees according to paragraph 1 shall be assessed and collected by the Industrial Property Office (“Office”). Section 2 Rates Rates of maintenance fees for a patent, maintenance fees for a European patent and maintenance fees for supplementary certificates are laid down in the tariff of maintenance fees, which is listed in the appendix to this Act. Section 3 Payer (1) The payer of maintenance fees for a patent shall be the patent holder. (2) The payer of maintenance fees for a European patent shall be the holder of the European patent with effects for the Czech Republic (“European patent”). (3) The payer of maintenance fees for supplementary certificates shall be the holder of the supplementary protection certificate for medicaments and for plant protection products (“supplementary certificate”). 1 Act No. 527/1990 Coll., on Inventions and Rationalisation Proposals, as amended by later regulations. -
Utility Model
Utility model An information brochure on utility model protection UTILITY MODEL PROTECTION | 3 Contents The utility model – the underrated industrial property right ................... 4 The most important differences between the utility model and the patent .... 5 Searches give you security.................................................... 6 Patent or utility model? Patent and utility model! ............................. 7 How to apply................................................................. 8 Your application has priority.................................................. 9 Cancellation proceedings – the utility model is put to the test ................ 10 Service.......................................................................11 4 | UTILITY MODEL PROTECTION The utility model – the underrated industrial property right You are looking for fast and low-cost The examination and grant of a patent protection for your invention? Then the usually takes several years. The utility model, utility model – the “little brother” of the in contrast, will be registered within a few patent – is the right thing for you. months after filing the application, provided the documents filed comply with the provi- Like the patent, it can protect all technical sions of the Utility Model Law. inventions, including also chemical sub- stances, food and medicinal products, except The IP right becomes effective upon registra- for processes (manufacturing and working tion and it gives you the same rights as a processes, measuring processes, and others). patent: exclusive right to use, produce and market your invention. You may prohibit any person from doing the same. UTILITY MODEL PROTECTION | 5 The most important differences between the utility model and the patent The utility model is an unexamined IP right. Another important difference to the patent is The registration procedure does not examine the “life” of a utility model. A patent can be novelty, inventive step and industrial maintained for 20 years, while a utility model applicability. -
“The Origin of Specis” (Patent Specifications) BASIC FACTS (A.K.A
The Origin of Specis (or, nearly everything you wanted to know about patents, but couldn’t be bothered asking) 22.Sep.2021 © Tony McStea 1992-2021 22.Sep.2021 About the Author… (with apologies to Gilbert and Sullivan) When I was a lad, I served a term As patent tech. assistant in a big paint firm I wrote applications and I argued and tried Patent offices to show that grant was justified And this sort of thing so suited me That now I’m patent attorney in industry. Acknowledgement My grateful thanks to all of you out there who helped me with this revised version by offering comments, corrections, criticisms, suggestions and advice, some of which I ignored, which is why the booklet still exists. The responsibility for any errors (not to mention the mediocre drawings and terrible jokes (or is it mediocre jokes and terrible drawings?)) is entirely mine. The responsibility for any views or opinions expressed herein is also entirely mine. N.B. Most costs mentioned herein were correct (more or less) at June, 2015, but, because of the tendency of official fees to fluctuation (and exchange rates to go up and down like yo-yos), and the consequent work of constantly adjusting them, they have been left as they are and are there to be general guides only. 22.Sep.2021 Note: changes to US Law On 16 March 2013 (thus missing by one day the Blessing of St. Patrick on the entire enterprise), the Leahy-Smith “America invents” Act (AIA), the most significant change to US patent law in half a century, came fully into effect. -
Patents and Standards
Patents and Standards A modern framework for IPR-based standardization FINAL REPORT A study prepared for the European Commission Directorate-General for Enterprise and Industry This study was carried out for the European Commission by and as part of the DISCLAIMER By the European Commission, Directorate-General for Enterprise and Industry The information and views set out in this publication are those of the author(s) and do not necessarily reflect the official opinion of the Commission. The Commission does not guarantee the accuracy of the data included in this study. Neither the Commission nor any person acting on the Commission’s behalf may be held responsible for the use which may be made of the information contained therein. ISBN 978-92-79-35991-0 DOI: 10.2769/90861 © European Union, 2014. All rights reserved. Certain parts are licensed under conditions to the EU. Reproduction is authorized provided the source is acknowledged. About ECSIP The European Competitiveness and Sustainable Industrial Policy Consortium, ECSIP Consortium for short, is the name chosen by the team of partners, subcontractors and individual experts that have agreed to work as one team for the purpose of the Framework Contract on ‘Industrial Competitiveness and Market Performance’. The Consortium is composed of Ecorys Netherlands (lead partner), Cambridge Econometrics, CASE, CSIL, Danish Technological Institute, Decision, Eindhoven University of Technology (ECIS), Euromonitor, Fratini Vergano, Frost & Sullivan, IDEA Consult, IFO Institute, MCI and wiiw, together with a group of 28 highly-skilled and specialised individuals. ECSIP Consortium p/a ECORYS Nederland BV Watermanweg 44 3067 GG Rotterdam P.O. Box 4175 3006 AD Rotterdam The Netherlands T. -
20100801 Tarifes
Schedule of Charges - April 2010 - EUR Official Professional EUROPEAN PATENTS Total fees1 fees EuroPCT Filing (regional phase of PCT) EuroPCT filing (electronic filing) 105 810 915 Requesting examination and paying designations 2170 270 2440 - Examination fee: 1645 € - Designation fee: 525 € Other charges upon filing - Extension fee: 102 € per country 102* -- 102* - Translation of specification from Spanish into English, (100 words) -- 22* 22* - Additional fee for each page in excess of 352 13* -- 13* - Claim fee, for each claim in excess of 15: From 16 to 50: 210€/claim 210* -- 210* In excess of 51: 525€/claim 525* -- 525* - Requesting supplementary European Search màx. 1150 270 màx. 1320 - Late filing of documents -- 100 100 - Proceedings related with claims' amendment under Rule 161 -- 270 270 EP Filing Standard EP filing 1210 1080 2290 - Filing fee: 105 € (electronic filing) - Search fee: 1105 € Other charges upon filing - Translation of specification from Spanish into English, (100 words) -- 22* 22* - Additional fee for each page in excess of 352 13* -- 13* - Claim fee, for each claim in excess of 15: From 16 to 50: 210€/claim 210* -- 210* In excess of 51: 525€/claim 525* -- 525* - Late filing of documents -- 100 100 Request Examination Requesting examination and paying designations 2005 270 2275 - Examination fee: 1480 € - Designation fee3: 525 € - Designation fee3: 90 € per country (maximum 630 €) Other charges when requesting examination - Extension fee: 102 € per country 102* -- 102* Examination Replying to Official Action -- 270 270 Grant4 Printing fee and filing of claim translations 830 350 1180 Other charges upon grant - Additional fee for each page in excess of 353 13* -- 13* - Translation of claims, each 100 words into French and German -- 50* 50* NOTE: The above professional fees do not include substantial patent work such as drafting applications, answering official actions, drafting amendments, arguments and statements of grounds, meeting with clients and the like. -
U.S. Patent and Trademark Office
U.S. Patent and Trademark Office Fiscal Year 2022 Congressional Justification May 2021 This Page is Intentionally Left Blank DEPARTMENT OF COMMERCE UNITED STATES PATENT AND TRADEMARK OFFICE Budget Estimates, Fiscal Year 2022 Congressional Justification Table of Contents Exhibit Number Exhibit Page Number 2 Organization Chart USPTO - 4 3 Executive Summary USPTO - 5 Patent and Trademark Businesses: Five-Year Horizon 3T Transfer Change Detail by Object Class USPTO - 19 4A Program Increases / Decreases / Terminations USPTO - 20 4T Transfer Summary Table USPTO - 22 5 Summary of Resource Requirements: Direct Obligations USPTO - 23 7 Summary of Financing USPTO - 25 8 Adjustments-to-Base USPTO - 26 Patent Program 10 Program and Performance: Direct Obligations USPTO - 28 12 Justification of Program and Performance (by Subactivity) USPTO - 29 13 Program Change for 2022 USPTO - 34 14 Program Change Personnel Detail USPTO - 35 15 Program Change Detail by Object Class USPTO - 41 Trademark Program 10 Program and Performance: Direct Obligations USPTO - 44 12 Justification of Program and Performance (by Subactivity) USPTO - 45 13 Program Change for 2022 USPTO - 50 14 Program Change Personnel Detail USPTO - 55 15 Program Change Detail by Object Class USPTO - 57 Intellectual Property Policy, Enforcement and Protection Program 10 Program and Performance: Direct Obligations USPTO - 60 12 Justification of Program and Performance (by Subactivity) USPTO - 61 Exhibit Number Exhibit Page Number 13 Program Change for 2022 USPTO - 65 14 Program Change Personnel -
Implementation of the Convention on the Grant of European Patents Act
International Portal of the University of Portal Internacional de la Universidad Alicante on Intellectual Property & de Alicante sobre Propiedad Industrial Information Society e Intelectual y Sociedad de la Información IMPLEMENTATION OF THE CONVENTION ON THE GRANT OF EUROPEAN PATENTS ACT. Unofficial translation Passed on 17 April 2002, enter into force on the day of entering into force of the accession of the Republic of Estonia to the Convention on the grant of European Patents (RT I 2002, 38, 233) Section 1. Scope of application of Act This Act provides for the legal status of European patents and patent applications in Estonia and regulates legal relations arising from the accession of the Republic of Estonia to the Convention on the grant of European Patents (European Patent Convention) not covered by the Patent Act (RT I 1994, 25, 406; 1998, 74, 1227; 107, 1768; 1999, 84, 764; 2001, 27, 151) or the said Convention. Section 2. Definitions For the purposes of this Act: 1) Convention means the Convention on the grant of European Patents (European Patent Convention), done at Munich on 5 October 1973; 2) Organisation means the European Patent Organisation as established by the Convention; 3) European Patent Office means the organ of the Organisation carrying out their task to grant European patents; 4) Contracting State means a contracting state of the Convention; 5) For the purposes of the Convention Estonian Patent Office means the central industrial property office in Estonia; 6) European patent means a patent granted by the European -
Faqs About the Unitary Patent System and Unitary Patent Court
FAQs About the Unitary Patent System and Unitary Patent Court Can pending EPO applicants select the UP option? Yes. The new system will apply to currently pending applications in the EPO that proceed to grant after the implementation date. How does an EPO applicant select the UP option? An EPO applicant can postpone the decision on whether to select the UP option or the national validation option until the application proceeds to grant. Applicants must then select the UP option within one month of the EPO grant date. EPO applicants who do not wish to obtain a UP or who want protection in countries that are not part of the UPS may elect to validate nationally after grant according to the current deadlines (three months after grant in most EPO members). EPO applicants can also select a combination of a UP and validating nationally in countries that are not part of the UPS. What are the translation requirements for the UP? Generally, the requirements will be less burdensome than for the current national validation or direct national filing routes. During the first twelve years of the UPS, only one translation will be necessary. Patents prosecuted in French or German must be translated into English. Patents prosecuted in English must be translated into any other EU language (not limited to French and German). After the transitional period, no translations will be required. What are the validation and maintenance costs? There is no validation fee. There is a single annual maintenance fee equivalent to the cost of four national renewal fees (UK, France, Germany and Netherlands). -
495/2008 Coll
____________________________________________________________ 495/2008 Coll. ACT of November 6, 2008 on maintenance fee for the patent, maintenance fee for the European patent with effects for the Slovak Republic and the maintenance fee for the supplementary protection certificate for medicinal and plant protection products and on amendment of some acts Amended by: 600/2008 Coll. Amended by: 519/2010 Coll. The National Council of the Slovak Republic has adopted the following Act: Title I Article 1 Subject-matter of the regulation This Act shall govern the amount and collecting the fee for the maintenance of the patent1) (hereinafter referred to as “maintenance fee for the patent”), the fee for maintenance of the European patent with effects for the Slovak Republic1) (hereinafter referred to as “maintenance fee for the European patent”), the fee for maintenance of the supplementary protection certificate for medicinal and plant protection products2) (hereinafter referred to as “maintenance fee for the supplementary protection certificate”). Article 2 Payer (1) The owner of the patent or a person authorised by the owner shall be the payer of the maintenance fee. (2) The owner of the European patent with effects for the Slovak Republic (hereinafter referred to as “European patent”) or a person authorised by the owner shall be the payer of the maintenance fee. (3) The owner of the supplementary protection certificate for medicinal and plant protection products (hereinafter referred to as “supplementary protection certificate”) or a person authorised by the owner shall be the payer of the maintenance fee. (4) If there are several payers, they are required to pay the maintenance fee for the patent, the maintenance fee for the European patent, maintenance fee for the supplementary protection certificate (hereinafter referred to as “maintenance fee”), they are obliged to pay it jointly and severally.