The document provides information on intellectual property (IP) practice, including:
1) HDP is the 10th largest US IP firm with over 110 attorneys across four offices. In 2018 it obtained the 6th highest number of utility patents.
2) It discusses strategies for freedom to operate (FTO) analyses such as patent searches, monitoring risks of infringement, and obtaining opinions of counsel. Litigation costs and risks are also reviewed.
3) Guidelines are presented for patent preparation and prosecution best practices, including ownership issues, duty of candor, claim drafting, means-plus-function language, and obviousness arguments.
European & us patent law module3 2013 updatedIP Dome
This document provides an overview of patentability requirements in the US and Europe. It discusses the US patent regime, including patentability, novelty, non-obviousness, and specific cases related to anticipation. It also touches on plant patents, hybrids, and the differences between filing dates and priority dates. Overall, the document outlines key concepts regarding patent eligibility and examines the standards for obtaining a patent in different jurisdictions.
The document discusses patentability requirements in the US, including utility, novelty, and non-obviousness. It provides details on the types of subject matter that can be patented, conditions for novelty like anticipation and statutory bars, and considerations for non-obviousness. It also discusses the European patent regime and takes questions.
This document provides a brief overview of US utility patent law and the patenting process. It discusses the different types of patents including design, plant, and utility patents. It describes the basic patenting timeline including filing a provisional or non-provisional patent application and undergoing examination. Key concepts like patentability requirements of utility, novelty, and non-obviousness are introduced. Cost estimates and strategies for obtaining and enforcing a patent are also summarized.
Patent in Living Organism (Speaking Roses International v. Controller General...Abhinandan Ray
According to Section 3 (j) of Indian Patent Act, 1970 plants and animals can't be a subject matter of patent in India and this case is related to this section.
The document discusses patents, including what they are, how they are obtained, and their key aspects and requirements. Some main points:
- Patents provide exclusive rights over inventions and protect creations of the human mind. They are granted by patent offices for new, inventive, and industrially applicable inventions.
- To be patented, inventions must be novel with an inventive step not obvious to others in the field. They must also have utility and be capable of industrial application.
- Patent applications undergo an examination process before being granted for a limited period of time (usually 20 years). Patents are territorial rights within the granting country or region.
- International agreements like the Patent Cooperation Treaty
The document summarizes key changes to patent law under the America Invents Act, including changing from a first-to-invent system to a first-inventor-to-file system. It discusses provisions around prior art exceptions, derivation proceedings, issues around the scope of prior art and inventor disclosures, and recommendations like filing early and considering pre-filing public disclosures.
This document discusses patent infringement and remedies under Indian law. It defines patent infringement as making, using, offering to sell, selling, or importing a patented product or process without permission. There are direct and indirect types of infringement. Certain uses for research or education are excluded. The patentee or assignee can file an infringement suit within 3 years. The plaintiff bears the burden of proof initially. Remedies for infringement include injunctions and damages or accounting of profits. Temporary injunctions require considering a prima facie case, balance of convenience, and irreparable loss. Several case laws are discussed, including ones related to linezolid patents, DTSi technology, the rejection of a patent for Gleevec, and actions for
The document discusses patentable subject matter under Indian and international law. It provides definitions of invention and outlines what can and cannot be patented according to the Indian Patents Act of 1970 and TRIPS agreement. It discusses exclusions from patentability including those that are frivolous, contrary to public order or morality, or mere discoveries with examples of each.
European & us patent law module3 2013 updatedIP Dome
This document provides an overview of patentability requirements in the US and Europe. It discusses the US patent regime, including patentability, novelty, non-obviousness, and specific cases related to anticipation. It also touches on plant patents, hybrids, and the differences between filing dates and priority dates. Overall, the document outlines key concepts regarding patent eligibility and examines the standards for obtaining a patent in different jurisdictions.
The document discusses patentability requirements in the US, including utility, novelty, and non-obviousness. It provides details on the types of subject matter that can be patented, conditions for novelty like anticipation and statutory bars, and considerations for non-obviousness. It also discusses the European patent regime and takes questions.
This document provides a brief overview of US utility patent law and the patenting process. It discusses the different types of patents including design, plant, and utility patents. It describes the basic patenting timeline including filing a provisional or non-provisional patent application and undergoing examination. Key concepts like patentability requirements of utility, novelty, and non-obviousness are introduced. Cost estimates and strategies for obtaining and enforcing a patent are also summarized.
Patent in Living Organism (Speaking Roses International v. Controller General...Abhinandan Ray
According to Section 3 (j) of Indian Patent Act, 1970 plants and animals can't be a subject matter of patent in India and this case is related to this section.
The document discusses patents, including what they are, how they are obtained, and their key aspects and requirements. Some main points:
- Patents provide exclusive rights over inventions and protect creations of the human mind. They are granted by patent offices for new, inventive, and industrially applicable inventions.
- To be patented, inventions must be novel with an inventive step not obvious to others in the field. They must also have utility and be capable of industrial application.
- Patent applications undergo an examination process before being granted for a limited period of time (usually 20 years). Patents are territorial rights within the granting country or region.
- International agreements like the Patent Cooperation Treaty
The document summarizes key changes to patent law under the America Invents Act, including changing from a first-to-invent system to a first-inventor-to-file system. It discusses provisions around prior art exceptions, derivation proceedings, issues around the scope of prior art and inventor disclosures, and recommendations like filing early and considering pre-filing public disclosures.
This document discusses patent infringement and remedies under Indian law. It defines patent infringement as making, using, offering to sell, selling, or importing a patented product or process without permission. There are direct and indirect types of infringement. Certain uses for research or education are excluded. The patentee or assignee can file an infringement suit within 3 years. The plaintiff bears the burden of proof initially. Remedies for infringement include injunctions and damages or accounting of profits. Temporary injunctions require considering a prima facie case, balance of convenience, and irreparable loss. Several case laws are discussed, including ones related to linezolid patents, DTSi technology, the rejection of a patent for Gleevec, and actions for
The document discusses patentable subject matter under Indian and international law. It provides definitions of invention and outlines what can and cannot be patented according to the Indian Patents Act of 1970 and TRIPS agreement. It discusses exclusions from patentability including those that are frivolous, contrary to public order or morality, or mere discoveries with examples of each.
Intellectual property law refers to creations of the mind such as inventions, literary works, and symbols. The US Constitution gives Congress the power to grant limited monopolies to authors and inventors via copyright and patent laws. There are several types of intellectual property including patents, copyrights, trademarks, and trade secrets. Patents protect new and useful processes, machines, manufactures, compositions of matter, and plant designs for a limited term. Obtaining a patent requires an application process to show the invention is novel, non-obvious, and adequately disclosed. The America Invents Act of 2011 modernized US patent law and changed it from a first-to-invent system to a first-inventor-to-file
The document provides an overview of patent law in India, including:
1) A patent grants an inventor exclusive rights to an invention that is novel, useful, and non-obvious.
2) India's patent law has evolved since the 1850s through several Acts, with the current Patents Act coming into force in 1970.
3) The Act provides for patents on both products and processes, with a term of 20 years, and includes pre- and post-grant opposition provisions.
This document provides an overview of inventorship issues in U.S. patent law. It discusses that the applicant for a patent must be the inventor, and that U.S. law requires having the correct inventors listed. It covers topics like conception, joint inventorship, derivation, identifying inventors, correcting inventorship, and standing. The document is intended to help practitioners properly determine inventorship when prosecuting patent applications.
Patent Law in India_What,How to get it regisgtered and protectedKrishan Singla
It describes the patent law in India and describes what comes and what does come under patent . In other words it defines what kind of inventions can be patented . In brief it contains the following topics:
-What is intellectual property
-Meaning of Patent
-Legislative Framework Patents
-Patent Law - Salient Features
-Safeguards in the Patent Law
-Definition of patentable invention
-Inventions not patentable
-Documenting invention
-Steps for obtaining a patent in India
-Rights of product patentee
-Rights of process patentee
-Renewal of patent
-Infringement of patent
-Patent Due Diligence
I’m so confused — what is prior art now? Marc Hubbard
How did the America Invents Act (AIA) change the definition of prior art when it switched the U.S. patent system from first-to-invent to first-to-file.
The document provides an overview of patentability requirements for various subject matters under Indian patent law. It discusses that to be patentable, an invention must not be excluded under Sections 3 and 4 of the Indian Patents Act, which include inventions that are not novel, are frivolous, contrary to morality, or relate to atomic energy or methods of agriculture. The document then describes various exclusions such as mere discoveries, arrangements of known elements, business methods, and traditional knowledge.
The document announces an upcoming seminar on navigating the risks and rewards of the America Invents Act for start-ups and entrepreneurs. The seminar will be held on October 27th, 2011 from 11:30 AM to 1:00 PM PST at Hantel Technologies in Hayward, CA. It will feature speaker Brian Eller from NC State who will provide an overview of the immediate and long term impacts of the America Invents Act on innovation and technology development, with relevance for medical devices. Registration is requested on EventBrite.
The document provides an introduction to patent law, including:
1) A patent is a legal document issued by a government that grants the right to prohibit others from making, using, or selling a claimed invention for a limited time in exchange for publicly disclosing the invention details.
2) The purpose of patent law is to promote science and useful arts by securing exclusive rights to authors and inventors for limited times.
3) Inventors seek patent protection for both offensive and defensive strategies related to investment, revenue, market protection, and preventing competitor patents.
The Patents Act of 1970 (as amended in 2005) governs patent procedures and intellectual property rights in India. Key points include:
- A patent provides an inventor the exclusive right to make, use, or sell an invention for a period of up to 20 years. To be patentable, an invention must be novel, non-obvious, and useful.
- The Act was amended in 2005 to comply with international agreements on intellectual property, removing distinctions between product and process patents and raising the patent term to 20 years.
- The process for obtaining a patent involves filing an application that is examined for compliance with patentability criteria before a patent is granted. Compulsory licensing provisions allow generic manufacturing
The document provides an overview of U.S. patent law history and current practice. It discusses key milestones in patent law such as the first known patent granted in 1491 in Florence, the inclusion of patent rights in the U.S. Constitution, and several Patent Acts that established the U.S. patent system. It also outlines the patent application process including filing provisional and non-provisional applications, and the examination of applications under key patentability requirements like novelty and non-obviousness. Key anatomy of a patent such as the claims, drawings, and descriptions are also summarized.
Indian patent act - 1970 - definitions, history, types, terms, inventions patentable and non-patentable, patent filling procedure, rights of a patentee, offences and penalties.
The document provides an update on US patent reform and the America Invents Act. Key points include:
- The bills passed the Senate and House with different provisions around fee diversion and USPTO budget authority.
- The Act moves the US to a first-to-file system with a one-year grace period and introduces several new post-issuance proceedings.
- It compares the changes between old and new §102 standards for novelty and prior art. The new §102(a) combines elements of the old §102(a)-(e) and the new §102(b) creates grace period exceptions.
- Best practices for applicants under the first-to-publish system include promptly filing a provision
The document summarizes the first case of compulsory licensing granted in India, between Bayer and Natco Pharmaceuticals regarding the drug Nexavar. The Controller of Patents granted the license to Natco after determining that Bayer's drug was not reasonably affordable in India. Some key points:
- Bayer's Nexavar treatment cost over $2,000/month while Natco's generic version cost $88/month.
- Bayer had not manufactured the drug in India or made it widely available.
- The license allows Natco to produce a generic version at a significantly lower cost, while still paying a 6% royalty to Bayer.
This document discusses patent infringement, including what it is, types of infringement, how to judge infringement, and potential consequences. Patent infringement occurs when someone makes, uses, or sells a patented invention without permission from the patent holder. There are two types of infringement: direct infringement involves directly using the patented invention, while indirect infringement involves supplying parts that can only be used with a patented invention. To determine if infringement occurred, a court will analyze the patent claims and see if they encompass the accused device or process. Potential consequences of infringement include barriers to innovation, damage to economic and legal systems, and financial remedies determined in court cases.
The document discusses joint research agreements (JRAs) and how they can be used to overcome prior art rejections under the CREATE Act. It explains that the CREATE Act allows commonly owned secret prior art or prior art from different owners involved in a JRA to be disqualified. The summary discusses requirements for invoking the CREATE Act during patent prosecution to overcome rejections and potential issues like double patenting rejections that could result.
At a recent Forresters And Knobbe Martens Seminar, Charlotte Teall (Forresters) and Dan Altman (Knobbe Martens) presented "Latest Developments in European Patent Law: How to Apply Them in Both the United States and Europe."
Presentation on Patent Law Basics by Dr. Kalyan C. Kankanala, Brain League IP...BananaIP Counsels
This document provides an overview of patent law basics including requirements for patentability, exclusions from patentable subject matter, international instruments governing patents, and examples to illustrate the concepts. It discusses topics such as inventor incentives, the patent regime, Indian patent law and amendments, patentability criteria of subject matter, novelty, non-obviousness, and specifications. Exclusions outlined include scientific principles, abstract ideas, and traditional knowledge. The examples demonstrate analyzing inventions in the context of the prior art.
This document provides an overview of patent law in India, including the history and mechanisms of intellectual property rights (IPR) and the Indian Patent Act of 1970. It describes what can be patented in India, the types of patents, the patent application process, and amendments made to the patent act over the years, including the Patent Amendment Acts of 1999, 2002, 2005, and 2010. The key purpose of patents is to protect inventions and provide exclusive commercial rights to inventors for a limited time.
The document discusses patent claims, describing them as the most important part of a patent that define the legal boundaries of an invention. It notes claims are difficult to write accurately and inexperienced individuals often fail to properly claim their invention or omit important parts. The document outlines what claims are, how they are structured, and their role in determining patentability, infringement, and evaluating other patents. It provides guidance on drafting clear and valuable claims, how claims evolve during examination, and how to evaluate a patent for infringement or invalidity.
Advanced Practice Under the American Invents Act (AIA).
Post Issuance Proceedings.
Kill Rates.
IPX.
Review Proceedings.
Insights and Lessons.
Trial Timeline.
What's Next?
Intellectual property law refers to creations of the mind such as inventions, literary works, and symbols. The US Constitution gives Congress the power to grant limited monopolies to authors and inventors via copyright and patent laws. There are several types of intellectual property including patents, copyrights, trademarks, and trade secrets. Patents protect new and useful processes, machines, manufactures, compositions of matter, and plant designs for a limited term. Obtaining a patent requires an application process to show the invention is novel, non-obvious, and adequately disclosed. The America Invents Act of 2011 modernized US patent law and changed it from a first-to-invent system to a first-inventor-to-file
The document provides an overview of patent law in India, including:
1) A patent grants an inventor exclusive rights to an invention that is novel, useful, and non-obvious.
2) India's patent law has evolved since the 1850s through several Acts, with the current Patents Act coming into force in 1970.
3) The Act provides for patents on both products and processes, with a term of 20 years, and includes pre- and post-grant opposition provisions.
This document provides an overview of inventorship issues in U.S. patent law. It discusses that the applicant for a patent must be the inventor, and that U.S. law requires having the correct inventors listed. It covers topics like conception, joint inventorship, derivation, identifying inventors, correcting inventorship, and standing. The document is intended to help practitioners properly determine inventorship when prosecuting patent applications.
Patent Law in India_What,How to get it regisgtered and protectedKrishan Singla
It describes the patent law in India and describes what comes and what does come under patent . In other words it defines what kind of inventions can be patented . In brief it contains the following topics:
-What is intellectual property
-Meaning of Patent
-Legislative Framework Patents
-Patent Law - Salient Features
-Safeguards in the Patent Law
-Definition of patentable invention
-Inventions not patentable
-Documenting invention
-Steps for obtaining a patent in India
-Rights of product patentee
-Rights of process patentee
-Renewal of patent
-Infringement of patent
-Patent Due Diligence
I’m so confused — what is prior art now? Marc Hubbard
How did the America Invents Act (AIA) change the definition of prior art when it switched the U.S. patent system from first-to-invent to first-to-file.
The document provides an overview of patentability requirements for various subject matters under Indian patent law. It discusses that to be patentable, an invention must not be excluded under Sections 3 and 4 of the Indian Patents Act, which include inventions that are not novel, are frivolous, contrary to morality, or relate to atomic energy or methods of agriculture. The document then describes various exclusions such as mere discoveries, arrangements of known elements, business methods, and traditional knowledge.
The document announces an upcoming seminar on navigating the risks and rewards of the America Invents Act for start-ups and entrepreneurs. The seminar will be held on October 27th, 2011 from 11:30 AM to 1:00 PM PST at Hantel Technologies in Hayward, CA. It will feature speaker Brian Eller from NC State who will provide an overview of the immediate and long term impacts of the America Invents Act on innovation and technology development, with relevance for medical devices. Registration is requested on EventBrite.
The document provides an introduction to patent law, including:
1) A patent is a legal document issued by a government that grants the right to prohibit others from making, using, or selling a claimed invention for a limited time in exchange for publicly disclosing the invention details.
2) The purpose of patent law is to promote science and useful arts by securing exclusive rights to authors and inventors for limited times.
3) Inventors seek patent protection for both offensive and defensive strategies related to investment, revenue, market protection, and preventing competitor patents.
The Patents Act of 1970 (as amended in 2005) governs patent procedures and intellectual property rights in India. Key points include:
- A patent provides an inventor the exclusive right to make, use, or sell an invention for a period of up to 20 years. To be patentable, an invention must be novel, non-obvious, and useful.
- The Act was amended in 2005 to comply with international agreements on intellectual property, removing distinctions between product and process patents and raising the patent term to 20 years.
- The process for obtaining a patent involves filing an application that is examined for compliance with patentability criteria before a patent is granted. Compulsory licensing provisions allow generic manufacturing
The document provides an overview of U.S. patent law history and current practice. It discusses key milestones in patent law such as the first known patent granted in 1491 in Florence, the inclusion of patent rights in the U.S. Constitution, and several Patent Acts that established the U.S. patent system. It also outlines the patent application process including filing provisional and non-provisional applications, and the examination of applications under key patentability requirements like novelty and non-obviousness. Key anatomy of a patent such as the claims, drawings, and descriptions are also summarized.
Indian patent act - 1970 - definitions, history, types, terms, inventions patentable and non-patentable, patent filling procedure, rights of a patentee, offences and penalties.
The document provides an update on US patent reform and the America Invents Act. Key points include:
- The bills passed the Senate and House with different provisions around fee diversion and USPTO budget authority.
- The Act moves the US to a first-to-file system with a one-year grace period and introduces several new post-issuance proceedings.
- It compares the changes between old and new §102 standards for novelty and prior art. The new §102(a) combines elements of the old §102(a)-(e) and the new §102(b) creates grace period exceptions.
- Best practices for applicants under the first-to-publish system include promptly filing a provision
The document summarizes the first case of compulsory licensing granted in India, between Bayer and Natco Pharmaceuticals regarding the drug Nexavar. The Controller of Patents granted the license to Natco after determining that Bayer's drug was not reasonably affordable in India. Some key points:
- Bayer's Nexavar treatment cost over $2,000/month while Natco's generic version cost $88/month.
- Bayer had not manufactured the drug in India or made it widely available.
- The license allows Natco to produce a generic version at a significantly lower cost, while still paying a 6% royalty to Bayer.
This document discusses patent infringement, including what it is, types of infringement, how to judge infringement, and potential consequences. Patent infringement occurs when someone makes, uses, or sells a patented invention without permission from the patent holder. There are two types of infringement: direct infringement involves directly using the patented invention, while indirect infringement involves supplying parts that can only be used with a patented invention. To determine if infringement occurred, a court will analyze the patent claims and see if they encompass the accused device or process. Potential consequences of infringement include barriers to innovation, damage to economic and legal systems, and financial remedies determined in court cases.
The document discusses joint research agreements (JRAs) and how they can be used to overcome prior art rejections under the CREATE Act. It explains that the CREATE Act allows commonly owned secret prior art or prior art from different owners involved in a JRA to be disqualified. The summary discusses requirements for invoking the CREATE Act during patent prosecution to overcome rejections and potential issues like double patenting rejections that could result.
At a recent Forresters And Knobbe Martens Seminar, Charlotte Teall (Forresters) and Dan Altman (Knobbe Martens) presented "Latest Developments in European Patent Law: How to Apply Them in Both the United States and Europe."
Presentation on Patent Law Basics by Dr. Kalyan C. Kankanala, Brain League IP...BananaIP Counsels
This document provides an overview of patent law basics including requirements for patentability, exclusions from patentable subject matter, international instruments governing patents, and examples to illustrate the concepts. It discusses topics such as inventor incentives, the patent regime, Indian patent law and amendments, patentability criteria of subject matter, novelty, non-obviousness, and specifications. Exclusions outlined include scientific principles, abstract ideas, and traditional knowledge. The examples demonstrate analyzing inventions in the context of the prior art.
This document provides an overview of patent law in India, including the history and mechanisms of intellectual property rights (IPR) and the Indian Patent Act of 1970. It describes what can be patented in India, the types of patents, the patent application process, and amendments made to the patent act over the years, including the Patent Amendment Acts of 1999, 2002, 2005, and 2010. The key purpose of patents is to protect inventions and provide exclusive commercial rights to inventors for a limited time.
The document discusses patent claims, describing them as the most important part of a patent that define the legal boundaries of an invention. It notes claims are difficult to write accurately and inexperienced individuals often fail to properly claim their invention or omit important parts. The document outlines what claims are, how they are structured, and their role in determining patentability, infringement, and evaluating other patents. It provides guidance on drafting clear and valuable claims, how claims evolve during examination, and how to evaluate a patent for infringement or invalidity.
Advanced Practice Under the American Invents Act (AIA).
Post Issuance Proceedings.
Kill Rates.
IPX.
Review Proceedings.
Insights and Lessons.
Trial Timeline.
What's Next?
Georgetown Univ. Law Center Conference: Post-Grant Patent Proceedings: Are th...WilmerHale
From The Georgetown University Law Center Conference: The Changing Patent Landscape held on March 23, 2015.
This presentation covers:
- Statistics on Post-Grant Proceedings
- Rule Changes for Post-Grant Proceedings
- IPR as Part of a Litigation Strategy
- Patent Owner’s Strategy in an IPR
- IPR Termination
Patent Law in 2014: Act fast or get left behindsteve_ritchey
A presentation on patent law fundamentals, the changes caused resulting from the America Invents Act, other topical patent law issues such as new developments on patentable subject matter, appellate review of claim constructions, and best practices
America Invents Act: Recent Changes to US Patent Law and PracticeGary M. Myles, Ph.D.
The document summarizes changes brought by the America Invents Act to U.S. patent law and practice. Some key changes include transitioning from a first-to-invent system to a first-inventor-to-file system, expanding the definition of prior art, creating new post-grant review proceedings like post-grant review and inter partes review, expanding prior user rights, and changing treatment of errors in inventorship. The changes aim to harmonize the U.S. system with other countries and improve patent quality and challenge procedures.
Patent prosecution, process and pitfalls by Benjamin Kuo (Wed, August 22, 2018)L15A
On Wed, August 22, 2018 Benjamin Kuo presented Intellectual Property "Patent Prosecution, Process and Pitfalls" CRASH Space.
https://blog.crashspace.org/events/intellectual-property-topics/
__________________________________________
Patent Prosecution, Process and Pitfalls
Eventually, every inventor is confronted with the decision to protect his technology by ways of a utility patent. Understanding the magnitude of the undertaking as well as the process and pitfalls involved can greatly reduce costs and (worse) avoid obtaining a useless patent.
In this talk, given by a patent attorney and former USPTO Examiner, the informed inventor will learn to distinguish patents from other forms of intellectual property, how to read a patent disclosure, the patent prosecution process and timeline, decide when and what to file, inner workings of the PTO black box, and how to find and work with a patent attorney.
__________________________________________
About the Presenter
Benjamin Kuo is a patent attorney and former computer engineer with a solo IP practice based in Los Angeles, specializing in helping smaller entities obtain IP protection. In addition to patent filings, he also supports litigation and consults with practitioners on Patent and Trademark Office issues. Before forming his own practice, he was a patent examiner for the USPTO, examining hundreds of computer networking applications and conducting numerous interviews with outside attorneys. Before working at the USPTO, he practiced at various law firms in the fields of patent prosecution, IP litigation, antitrust litigation, and federal corrupt practices act investigations. He is fluent in Mandarin Chinese and is licensed in California and before the USPTO. See more at benasaur.com/law.
The document discusses various third-party challenges to patents and patent applications that can be filed with the USPTO, including inter partes review (IPR), post grant review (PGR), covered business method patent review (CBM), preissuance submissions, and derivation proceedings. It provides details on the standards for instituting each proceeding, who can file, applicable grounds, timing requirements, procedures, and differences between the proceedings. USPTO fees for IPR are around $25k with typical total costs to completion of $350k-$700k. The overall success rate of IPRs is very high for petitioners, with around 85% of petitions granted and 60% of all claims found unpatent
American Invents Act (AIA) Overview.
AIA Transitions.
Changes.
Post Issuance Proceedings.
What You Need For a Patent.
Comparisons.
First Inventor to File with Grace (FTFG).
Prosecution Under FTFG.
Topics covered in this month’s patent prosecution presentation include a discussion of the new extended missing parts program, the Microsoft v. i4i case in which the clear and convincing standard for the presumption of validity is being challenged, the Costco v. Omega case regarding foreign first sale doctrine, patent office appeals practice, and joint infringement.
IP-301 POST-GRANT REVIEW TRIALS 2022 - Things to Consider Before You FileFinancial Poise
This segment will delve into considerations that come into play when filing or responding to post-grant review proceedings. These considerations include issues of real party in interest, timing, and substantive arguments.
Part of the webinar series: IP-301 POST-GRANT REVIEW TRIALS 2022
See more at https://www.financialpoise.com/webinars/
Five major differences between IPRs and invalidation proceedingsAlexandraPuYang
Alexandra Yang of Fangda Partners examines the differences and similarities between IPRs in the U.S. and invalidation proceedings before the CNIPA to give U.S. practitioners and clients a clear picture of the patent invalidation proceedings in China.
Picking someone to write your patent is like picking a mechanic to fix your car. Unless you know something about patents (or cars) – you don’t know what you’ve bought until a long time after you have paid.
I started writing patents over 12 years ago. This presentation includes tips derived from my experience, as well as a primer on patents and the process for getting patents.
Patent Law Review - IP Year in Review CLE v2Bryan Beel
This document provides a summary of a presentation on recent developments in patent law given to the Oregon State Bar Intellectual Property Section. It discusses several topics, including proposed patent legislation, practice before the International Trade Commission and Patent and Trademark Office, as well as recent decisions from the Federal Circuit and Supreme Court that have impacted patent law. The presentation was delivered by Bryan Beel of Perkins Coie LLP on February 14, 2014.
PGRT Basics (Series: IP 301 Post-Grant Review Trials 2020)Financial Poise
This segment will discuss the statutory and procedural background of post-grant review proceedings. It will discuss the types of proceedings available and provide a high-level discussion of how the proceedings are conducted.
To view the accompanying webinar, go to: https://www.financialpoise.com/financial-poise-webinars/pgrt-basics-2020/
IP-301: Post-Grant Review Trials 2020 - Interplay With District Court LitigationFinancial Poise
This segment, though last, is arguably the most important. It will discuss issues that come into being as a result of co-pending proceedings with U.S. district court litigation. These issues include estoppel, claim construction, and validity determinations.
To view the accompanying webinar, go to: https://www.financialpoise.com/financial-poise-webinars/interplay-with-district-court-litigation-2020/
The document summarizes several topics related to patent prosecution ethics:
1) It discusses a recent Supreme Court ruling on claim construction appeals and the implications for patent prosecutors.
2) It reviews potential conflicts of interest issues including subject matter conflicts when representing competitors and inventor representation conflicts.
3) It analyzes cases where attorneys failed to properly supervise staff, comply with signature requirements, or properly handle priority claims which resulted in disciplinary actions.
Things to Consider Before You File (Series: IP 301 Post-Grant Review Trials 2...Financial Poise
This segment will delve into considerations that come into play when filing or responding to post-grant review proceedings. These considerations include issues of real party in interest, timing, and substantive arguments.
To view the accompanying webinar, go to: https://www.financialpoise.com/financial-poise-webinars/things-to-consider-before-you-file-2020/
The document provides an overview of the U.S. patent process from conception of an invention to filing a patent application. It discusses key steps and considerations including scientific research and discovery, disclosure to a technology transfer office, evaluation of patentability, drafting the application, and filing as a provisional or non-provisional application. Important dates, prior art, record keeping, evaluation factors, and application types and strategies are covered in detail.
MBHB-Webinar-PTAB-Williams-Schafer-FINAL-02.25.15Andrew Williams
The document provides an overview of practical considerations for petitioners and patent holders in inter partes review proceedings before the Patent Trial and Appeal Board (PTAB). It discusses proactive and reactive petitions, statutory bars, real parties in interest, patent owner preliminary responses, and motions to amend claims. The document outlines key factors to consider for each topic, such as prior art searches, claim construction, controlling precedent cases, and evidentiary standards.
Lifting the Corporate Veil. Power Point Presentationseri bangash
"Lifting the Corporate Veil" is a legal concept that refers to the judicial act of disregarding the separate legal personality of a corporation or limited liability company (LLC). Normally, a corporation is considered a legal entity separate from its shareholders or members, meaning that the personal assets of shareholders or members are protected from the liabilities of the corporation. However, there are certain situations where courts may decide to "pierce" or "lift" the corporate veil, holding shareholders or members personally liable for the debts or actions of the corporation.
Here are some common scenarios in which courts might lift the corporate veil:
Fraud or Illegality: If shareholders or members use the corporate structure to perpetrate fraud, evade legal obligations, or engage in illegal activities, courts may disregard the corporate entity and hold those individuals personally liable.
Undercapitalization: If a corporation is formed with insufficient capital to conduct its intended business and meet its foreseeable liabilities, and this lack of capitalization results in harm to creditors or other parties, courts may lift the corporate veil to hold shareholders or members liable.
Failure to Observe Corporate Formalities: Corporations and LLCs are required to observe certain formalities, such as holding regular meetings, maintaining separate financial records, and avoiding commingling of personal and corporate assets. If these formalities are not observed and the corporate structure is used as a mere façade, courts may disregard the corporate entity.
Alter Ego: If there is such a unity of interest and ownership between the corporation and its shareholders or members that the separate personalities of the corporation and the individuals no longer exist, courts may treat the corporation as the alter ego of its owners and hold them personally liable.
Group Enterprises: In some cases, where multiple corporations are closely related or form part of a single economic unit, courts may pierce the corporate veil to achieve equity, particularly if one corporation's actions harm creditors or other stakeholders and the corporate structure is being used to shield culpable parties from liability.
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5. • Investigation to determine if you infringe patents of others
• Expensive process but necessary for commercialization
Freedom To Operate (FTO)
5
6. • Source: PwC 2017 Patent Litigation Study (May 2017)
FTO - Patent Damages in U.S.
6
7. • Keytruda: Merck’s cancer immunotherapy
• Annual sales: ~$700M
• Merck settles with BMS to pay $625M for past
patent infringement.
• In addition, Merck pays royalty for future sales.
Patent Infringement Case
7
vs.
8. • Samsung Galaxy: Sued for utility and design
patent & trade dress infringement
• Apple design patents: Round corner designs
• Damages: $1B $399M Settled
Design Infringement Case
8
vs.
9. • Oculus (Facebook): Sued for breach of non-
disclosure agreement (NDA) and copyright
infringement
• Damages: $500M (District Court, TX) for TM and
copyright infringement Settled
TM/Copyright/Trade Secret Case
9
11. • Litigation costs
• Infringement – lost profit, reasonable royalty
• Enhanced damage (X3) – willful infringement
• Awards of Attorney Fees – exceptional case
– Octane Fitness Supreme Court case
Total Expense
11
12. Willful Infringement & Opinion Of Counsel
12
• Willful Infringement
– Enhanced damage (X3)
– Halo Supreme Court decision: lower threshold for willful infringement
Award of enhanced damages was within the discretion of the trial court
"Totality of the Circumstances" Framework
• FTO Assessment & Opinion of Counsel
– What is opinion of counsel?
– Opinion of counsel valuable even if not required
• Minimize written record including emails
13. Attorney-Client Privilege
13
• Attorney-Client Privilege
– Promote frank and full discussions with counsel
• A-C Privilege Waiver
– A privileged communication shared with third parties
– Email c.c. issues
• “PRIVILEGED AND CONFIDENTIAL” works all the time?
14. Admission Against Interest (AAI)
14
• AAI is difficult to reverse. Avoid AAI!
• Do not create a document (including an email)
commenting on patentability verbal discussion!
15. Design Around v. Invalidation
15
• Cease and Desist letter Then what to do?
– Stop manufacturing/using & design around
– Keep using the invention and initiate invalidation proceeding(s)
• Design Around
– Difficulty of design around & FTO necessity (e.g., bolt v. drug)
• Patent Invalidation
– Court litigation
– AIA proceedings: PGR/IPR/CBM
– U.S. Patent Office: Ex Parte Reexamination
16. Patent Invalidation
16
Ex Parte
Reexamination
Inter Partes Review
(IPR)
Post-Grant
Review (PGR)
No third party participation Petitioner participates in the proceeding.
Anonymous submission
possible
Need to identify parties in interest
Anytime after patent
issuance
Pre-AIA patent: Anytime
Post-AIA patent: 9 months after
patent issuance
AIA patents only:
Within 9 months from
patent issuance
No Estoppel Estoppel
$6,000 PTO fee IPR: $30,000 and up/ PGR: $38,000 and up
Relatively easy to prepare Petition needs to be well prepared.
Not appealable Appealable to Federal Circuit
No deadline Final decision within 1 year from institution
17. Petition
Filed
(19 Feb 19)
PATENTEE
(Optional)
Preliminary
Response
(19 May 19)
IPR
Institution
Decision
(Aug 2019)
PATENTEE
Response &
Motion to
Amend Claims
(Nov 2019)
Petitioner
Reply to PO
Response
(Feb 2020)
PATENTEE
Reply to Opposition
to Amendment
(Feb 2020)
Oral
Hearing
Final
Written
Decision
(Aug 2020)
PO
Discovery
Period
Petitioner
Discovery
Period
PO
Discovery
Period
Period for
Observations &
Motions to Exclude
Evidence
3 Months
Petition Phase
IPR Timeline
3 Months 3 Months 3 Months 1 Month
Hearing set
on request
Trial Phase: No more than 12 months
20. Formal Papers
20
• Documents Requiring Signature(s) for US Application :
1) Declaration & Assignment
2) Power of Attorney (37 CFR 1.34. Acting in a representative capacity)
• Practice Tip: Submit the documents early!
many issues are caused by late filing or no filing.
– Declaration: Unavailable/disgruntled inventors
Substitute statement
– Assignment: Results in co-ownership (e.g., company and inventor)
– Co-ownership issues: Transfer of the patent, Standing to sue (case law)
21. 1. Patent Exploitation in U.S.
a) Each joint owner can exploit without permission of
others
b) No duty to share royalties
2. Patent Enforcement in U.S.
a) All joint owners must join suit
b) Other owners can grant license (circumvention)
Avoid Joint Ownership!
21
22. • Rule 56:
– A duty of candor and good faith in dealing with the Office
• Violation of Rule 56:
– Patent: Unenforceable
– Family patents: The doctrine of the fruit of the poisonous tree
• IDS Submission:
– Never hide “material info”
– When in doubt, just submit the info
Inequitable Conduct
22
23. IDS (Information Disclosure Statement)
23
Filing
First OA
on merit
Final OA
on merit
RCE First OA
Notice of
Allowance
Patent
Issuance
No fee
1. Gov. fee, or
2. No fee within 3
months from
foreign OA
Gov. fee,
even within 3
months from
foreign OA
No fee
1. Gov. fee, or
2. No fee within 3
months from
foreign OA
1. RCE + IDS
2. Quick Pass IDS (after
paying issue fee)
3. IDS without RCE (?)
1. IDS submission issues:
– Submit Foreign Office Actions? Search Reports?
– Category “A” (background) references?
– Non-prior art documents?
– RCE filing just for IDS submission?
2. IDS Timeline issues:
25. Missed 1-year Due Date or
Filings for Minor Improvements?
25
Filing 12 months
priority due
18 months
publication
30 months
Non-provisional or
PCT Application
with priority claim
Application by same
assignee:
§102(b)(2) exception
Application by same
inventor:
§102(b)(1) exception
Within 6 months from the
1 year date: An application
(with the same invention
or minor improvements)
can be filed if the assignee
is the same.
Within 12 months from the
publication date: An
application (with the same
invention or minor
improvements) can be filed if
the inventor is the same.
Filing 30 months
PCT National Phase
After 30 mo. due date: Petition to revive an unintentionally
abandoned application with an application
26. 1. Application for improvements before 1-year from patent
publication Continuation-in-part (CIP) filing
2. Application for improvements after 1-year from patent
publication New filing
3. New Data (supporting the claimed invention): CIP or
§1.132 Declaration?
a) CIP filing with the data
b) §1.132 Declaration for the pending application – MPEP 706.01
“Evidence traversing rejections, when timely presented, must be
considered by the examiner whenever present.”
New filing v. CIP v. §1.132 Declaration
26
27. Incorporation by reference
27
Use of “Incorporation By Reference”
– MPEP 608.01(p): An application for a patent when filed may
incorporate “essential material” by reference to (1) a U.S.
patent, or (2) a U.S. patent application publication.
– Applicant can import the limitations from the cited
patents/application.
– Example: Paice v. Ford Motor, 881 F.3d 894 (2018)
“This application discloses a number of improvements over
the hybrid vehicles disclosed in the inventor’s U.S. 5,343,970,
which is incorporated herein by this reference.”
28. Present Invention
28
• Avoid the term “invention”?
– Broad terms in claims can be interpreted narrowly because of
the term “invention” in the specification – Harris Corp. v.
Ericsson, 417 F.3d 1241 (Fed. Cir. 2005)
– Use terms such as “embodiment” instead of “invention”
– Terms to avoid: “the present invention”, “invention”, “object
of the invention”
29. Indefiniteness – Reasonable certainty
• Selection of Terms:
– Think twice before using generic descriptions: For example,
“high (or hot) temperature”, “poorly soluble”, “derivative”,
“analog”, “hydrophobic”, “stabilizing agent”, etc.
• Use definitions:
– For example: "Poorly water soluble drug" means a drug that has
a water solubility of less than 1 part in 30 parts of water.
• Include specific examples:
– For example: Examples of the poorly water soluble drugs
include, but are not limited to, famotidine, sildenafil, buspirone
and troglitazone.
29
30. Means-plus-function
30
• 35 U.S.C. 112(f):
– Means-plus-function language: limited to “corresponding
structure” described in the spec.
– No corresponding structure in the spec the claim is
invalid as being indefinite.
• Generic placeholders invoking 35 U.S.C. 112(f):
– Mechanism for, module for, device for, unit for, component
for, element for, member for, apparatus for, machine for,
system for
31. Claim Drafting Practice
31
• Telescoping claim set: broad claims coupled with narrow
claims
• Useful to enforce the patent
• Useful to defend the patent (e.g., IPR/PGR)
• MPF and Functional Language Not good??
• Useful to have both clearly defined claims and MPF/functional claims
• Broadest reasonable interpretation in PTO examination: Useful to add
definitions to the specification
• Method claim drafting Remember “single entity rule”!!
32. Preamble – Limiting Effects?
32
MPEP 2112.01:
The purpose or intended use of the invention in the preamble no limiting effect
33. Claim Drafting – Example
33
• A method for making delicious ramen to prevent swelling of
noodles and extra energy consumption, comprising:
1) measuring and adding water to a pot;
2) boiling water;
3) spraying soup base powders over the boiling water to
cause faster boiling;
4) pushing dried vegetables into the water for fast swelling;
5) eating the delicious ramen.
• A method for making delicious ramen to prevent swelling of
noodles and extra energy consumption, comprising:
1) measuring and adding water to a pot;
2) boiling water;
3) spraying soup base powders over the boiling water to
cause faster boiling;
4) pushing dried vegetables into the water for fast swelling;
5) eating the delicious ramen.
Simple preamble!
Simplify method steps!
Define action step only!
Single infringer rule!
Avoid sequence specific method!
34. Novelty – Anticipation
34
• Anticipation requirement: A claim is anticipated only if each
and every element as set forth in the claim is found
• Overlapping range: Not necessarily anticipatory
– Ineos USA LLC v. Berry Plastics Corp., 783 F.3d 865, 114 USPQ2d 1568
(Fed. Cir. 2015): When the prior art discloses its own range, rather
than a specific point, then the prior art is only anticipatory if it
describes the claimed range with sufficient specificity.
35. Prima Facie Obviousness
35
• PFO = Burden shifting ping-pong
• Part 1: PTO establishment of prima facie obviousness (PFO)
– The examiner bears the initial burden of factually supporting any
prima facie conclusion of obviousness.
– If the examiner does not produce a prima facie case, the applicant is
under no obligation to submit evidence of non-obviousness.
• Part 2: Applicant’s rebuttal on PFO
– Applicant may rebut the PFO presumption with evidence of
unexpected results and secondary considerations to support non-
obviousness.
36. Prima Facie Obviousness Case
36
• In re Grabiak, 769 F2d 729 (CAFC, 1985)
Prior Art (Howe) Claim 1
- Howe + Secondary reference showing O to S switch
- Court: No establishment of PFO
- Remember: non-obviousness ≠ inventiveness
37. PFO v. Data
37
• Response to an obviousness rejection
– Argue non-establishment of PFO
– Unexpected outcomes, particularly data
• Do we want to argue unexpected outcomes?
• Do we want/need to submit data as §1.132 declaration?
• PFO v. Unexpected Outcomes (data)
– What if you have both arguments, PFO and data?
• Is it better to argue both?
• Is it a case of commercial importance? Budget v. Output
38. Common Sense/Ordinary creativity
38
• Obviousness rejection based on “common sense/ordinary
creativity” may not be a good enough reason to reject a
claim as being obvious.
– Arendi SARL v. Apple:
• Common sense “cannot be used as a wholesale substitute for
reasoned analysis and evidentiary support”
– DSS Technology Management v. Apple:
• “Ordinary creativity” was not a good enough reason to find the
patent obvious
39. Inherency in Obviousness
39
• Inherency in novelty v. Inherency in obviousness
– MPEP 2112: Something which is old does not become patentable upon the discovery of
a new property.
• Obviousness “cannot be predicated on what is unknown,” and unknown
characteristics of the prior art do not constitute a teaching.
• Honeywell v. Mexichem
– “dismissing properties of the claimed invention as merely inherent, without further
consideration as to unpredictability and unexpectedness, erred as a matter of law.”
40. Prosecution Disclaimer
40
• Admissions as Prior Art (MPEP 2152)
Make background descriptions short!
• Prosecution Disclaimer
– Specification descriptions: “present invention,” “the objective of the
invention”
– Arguments in a response
– Arguments in IPR
41. • Expiration date: Determine the expiration of patents
• Patent Term Adjustment/Extension: PTA v. PTE
Patent Term & PTA
41
Patent Term Adjustment (PTA)
under 35 USC §154
Patent Term Extension (PTE)
under 35 USC §156
Eligibility Any Issued Patents Drug & Device Patents
Delay Patent Office Examination FDA Regulatory Review
Calculation 14 + 4 + 4 + 4 Rule ½ Clinical Trial + FDA Review
Terminal
Disclaimer
Reduces PTA No Reduction
Maximum
Term
PTO Delay (A+B+C periods) Five Years
42. Restriction Requirement
(Continuation v. Divisional)
42
Restriction
Requirement
Allowance &
Rejoinder
Election of a group with traverse
Traverse the restriction
US non-provisional:
No independent and
distinct inventions
PCT Nat’l phase:
“Unity of invention”
standard requiring
special technical
features
Withdrawal of restriction,
• Advantage: No divisional filing(s)
• Disadvantage: Continuation
filings only (which is subject to
double patenting rejection that
may require terminal disclaimer)
Maintained rejection Wasted
time and money for the response.
Divisional
Application
(for unelected
inventions)
• Advantage: No double patenting
rejection Full PTA extension
• Disadvantage: New filing costs
Election of a group without traverse
43. Total Claim Number
43
• National phase of a PCT application containing 40 claims:
(1) a product (20 claims)
(2) a method of using the product (10 claims)
(3) a method of making the product (10 claims)
– Preliminary Amendment & Claim Fee
– 312 Amendment Strategy (after allowance amendment)
• Why do we need more claims?
– Higher burden for patent challenger (in IPR and litigation)
– No extra maintenance costs
44. Response to Final Rejection
44
Final
Rejection
After Final
Response
After Final
Consideration
Pilot (AFCP) 2.0
RCE (Request for
Continued
Examination)
Appeal
Pre-Appeal Brief
Review Request
Continuation/
Divisional
Abandonment
Relatively simple amendment/
response (for advisory action)
Narrowing (minor) claim
amendments + interview
requirement
New arguments/amendments +
RCE fee renewed examination
Review by Appeal Board
Review by three examiners
(for apparent errors)
For examination of new claims
45. PTAB Appeal Strategy
45
Notice of Appeal +
Fee
Appeal
Brief
(within 2
months)Pre-Appeal
Conference
Examiner’s
Answer
Appeal
Forwarding fee
+ Optional
Reply Brief
(within 2
months)
Decision
by
Appeal
Board
Notice of Allowance
or Re-open prosecution
with new rejection(s)
Optional request
for oral hearing
with fee
OR
Any claims twice rejected
(e.g., final OA or first OA after RCE)
RCE or continuation can be filed
any time during the appeal.
46. U.S. Design Patent
46
Utility Patent Design Patent
Protects construction or function, not
appearance
Protects appearance, not construction or
function
3.5/7.5/11.5 year maintenance fees No maintenance fees
Allows product to be marked patent
pending
Allows product to be marked patent
pending
20 years from the filing date 15 years from issuance
Usually harder to get and more
expensive than a design patent
Usually easier to get and less expensive
than a utility patent
Allows recovery of infringer’s profits
• Protection: The aesthetic appearance of a product
• Patent Term: 15 years from issuance