The document discusses proposed rule changes and initiatives at the US Patent and Trademark Office (USPTO) to address issues with patent examination including pendency, quality, and keeping up with growth. Specifically, it notes the USPTO has hired more examiners, formed a central re-examination unit, extended second-layer review office wide, collected more software prior art, changed the patent academy, instituted examiner re-certification, allowed telecommuting, reduced allowance rates, and reduced error rates in patent allowance. It also shows data on pendency and inventory by technology area.
SKGF_Presentation_What You Need To Know About The Proposed USPTO Rule Changes...SterneKessler
The document discusses proposed rule changes and initiatives at the USPTO aimed at addressing issues related to patent application pendency, quality, and backlog. Specifically, it outlines proposed rules that would limit continuing applications and requests for continued examination by requiring additional showings for second or subsequent filings. It also discusses a proposed rule change to allow examiners to focus initial examination on representative claims designated by the applicant and defer examination of non-designated claims. The document provides examples and recommendations for practitioners regarding the proposed changes.
Indian Patent Office Status of Granted Patents| Patent Prosecution Law Firm in India
If you need business advisory services, you can refer to our Business Accelerator (TechCorpCapital), our law firm (TechCorpLegal) and our tech business consultancy (Tech Corp International Consultants, Singapore).
For technology specific advisory, you can refer to our premium service offerings for Mobile Applications, Social Media & Cyber Laws (CyberCorpLegal) and Pharmaceuticals, Biotechnology, Food & Healthcare (BioCorpLegal).
To know more about us, get connected with us on LinkedIn or mail us at info [at] techcorplegal [dot] com
The document provides guidelines for examination of patent applications in the field of pharmaceuticals in India. It discusses the historical development of pharmaceutical patenting in India and key provisions of Indian patent law. It covers assessment of inventions, novelty, inventive step, industrial applicability, non-patentable subject matter, and sufficiency of disclosure and claims. The guidelines are intended to help patent examiners achieve consistent examination standards and introduce harmonious practice.
Navigating Patents- Law and Process to FileIncuba8
The document discusses several international intellectual property treaties and conventions:
1. WIPO administers many intellectual property treaties and helps set up national IP laws.
2. The Paris Convention established procedures for filing internationally.
3. The Patent Cooperation Treaty provides an international filing system and 18-month publication.
4. TRIPS established more uniform global IP protections and enforcement as part of WTO agreements. Members must provide patents, copyrights, trademarks and enforcement.
UNCTAD was established in 1964 as a permanent intergovernmental body within the UN with 194 member countries. Its goals are to maximize trade, investment, and development opportunities for developing countries. It is headquartered in Geneva and oversees committees on commodities, manufactures, shipping, and other areas related to promoting international trade and formulating trade policies. UNCTAD's main functions include promoting global trade, establishing trade principles and policies, and reviewing and coordinating activities of other institutions to serve as a center for harmonious trade relations.
This slide deck is prepared by Mindy Bickel, a USPTO employee since 1989. Mindy works with innovators, entrepreneurs and local educators in and around New York City, providing them with appropriate information and resources offered by the USPTO and the Department of Commerce. This slide was used for a CoInvent event on Sept. 4th, 2014.
Intellectual property rights(I.P.R.) and traditional knowledge protection of ...Abhishek Singh
This document discusses traditional knowledge protection and provides examples of biopiracy cases involving neem, turmeric, and other plants from India. It describes how traditional knowledge from India regarding the medical properties of plants like neem and turmeric was patented in other countries. For example, the US Patent and Trademark Office granted a patent for wound healing properties of turmeric, despite it being used traditionally in India for thousands of years. Both these patents were later revoked after India provided evidence of prior art. The document advocates for protecting traditional knowledge from misappropriation and promoting its sustainable use.
This document provides an overview of various types of intellectual property rights including copyright, patents, trademarks, laws of confidence, design rights, and passing off. It discusses each type of intellectual property right in 1-2 paragraphs, outlining what they protect, relevant laws and statutes, and duration of protection. For each type of intellectual property, it also provides 1-2 sentences on how they are administered in Tanzania.
SKGF_Presentation_What You Need To Know About The Proposed USPTO Rule Changes...SterneKessler
The document discusses proposed rule changes and initiatives at the USPTO aimed at addressing issues related to patent application pendency, quality, and backlog. Specifically, it outlines proposed rules that would limit continuing applications and requests for continued examination by requiring additional showings for second or subsequent filings. It also discusses a proposed rule change to allow examiners to focus initial examination on representative claims designated by the applicant and defer examination of non-designated claims. The document provides examples and recommendations for practitioners regarding the proposed changes.
Indian Patent Office Status of Granted Patents| Patent Prosecution Law Firm in India
If you need business advisory services, you can refer to our Business Accelerator (TechCorpCapital), our law firm (TechCorpLegal) and our tech business consultancy (Tech Corp International Consultants, Singapore).
For technology specific advisory, you can refer to our premium service offerings for Mobile Applications, Social Media & Cyber Laws (CyberCorpLegal) and Pharmaceuticals, Biotechnology, Food & Healthcare (BioCorpLegal).
To know more about us, get connected with us on LinkedIn or mail us at info [at] techcorplegal [dot] com
The document provides guidelines for examination of patent applications in the field of pharmaceuticals in India. It discusses the historical development of pharmaceutical patenting in India and key provisions of Indian patent law. It covers assessment of inventions, novelty, inventive step, industrial applicability, non-patentable subject matter, and sufficiency of disclosure and claims. The guidelines are intended to help patent examiners achieve consistent examination standards and introduce harmonious practice.
Navigating Patents- Law and Process to FileIncuba8
The document discusses several international intellectual property treaties and conventions:
1. WIPO administers many intellectual property treaties and helps set up national IP laws.
2. The Paris Convention established procedures for filing internationally.
3. The Patent Cooperation Treaty provides an international filing system and 18-month publication.
4. TRIPS established more uniform global IP protections and enforcement as part of WTO agreements. Members must provide patents, copyrights, trademarks and enforcement.
UNCTAD was established in 1964 as a permanent intergovernmental body within the UN with 194 member countries. Its goals are to maximize trade, investment, and development opportunities for developing countries. It is headquartered in Geneva and oversees committees on commodities, manufactures, shipping, and other areas related to promoting international trade and formulating trade policies. UNCTAD's main functions include promoting global trade, establishing trade principles and policies, and reviewing and coordinating activities of other institutions to serve as a center for harmonious trade relations.
This slide deck is prepared by Mindy Bickel, a USPTO employee since 1989. Mindy works with innovators, entrepreneurs and local educators in and around New York City, providing them with appropriate information and resources offered by the USPTO and the Department of Commerce. This slide was used for a CoInvent event on Sept. 4th, 2014.
Intellectual property rights(I.P.R.) and traditional knowledge protection of ...Abhishek Singh
This document discusses traditional knowledge protection and provides examples of biopiracy cases involving neem, turmeric, and other plants from India. It describes how traditional knowledge from India regarding the medical properties of plants like neem and turmeric was patented in other countries. For example, the US Patent and Trademark Office granted a patent for wound healing properties of turmeric, despite it being used traditionally in India for thousands of years. Both these patents were later revoked after India provided evidence of prior art. The document advocates for protecting traditional knowledge from misappropriation and promoting its sustainable use.
This document provides an overview of various types of intellectual property rights including copyright, patents, trademarks, laws of confidence, design rights, and passing off. It discusses each type of intellectual property right in 1-2 paragraphs, outlining what they protect, relevant laws and statutes, and duration of protection. For each type of intellectual property, it also provides 1-2 sentences on how they are administered in Tanzania.
Focus on Pharma: Creating, Protecting & Enforcing High-Value IP AssetsSterneKessler
A two-day conference held by Sterne, Kessler, Goldstein & Fox P.L.L.C., which focused on on recent trends in substantive case law, their impact on patent prosecution and examination, and implications regarding the enforcement of patents in the pharmaceutical and biopharmaceutical industry.
This document summarizes a USPTO Bio/Chem/Pharma Customer Partnership meeting in September 2006. About 100 people attended in person and 40 attended virtually. Key topics discussed included recent changes to restriction practice, data on restriction petition outcomes, new accelerated examination rules, the examination of bioinformatics cases, and upcoming proposed rule changes regarding claims, continuations, IDS practice and Markush claims. Speakers from various technology centers and art units provided updates in their areas. Attendees engaged in discussion and questions.
SKGF_Advisory_US Design Patents Strengthened by Recent Federal Circuit Ruling...SterneKessler
The Federal Circuit issued a decision strengthening US design patents. It threw out the "point of novelty" test for infringement and returned to a test of whether the accused design is "substantially the same as" or a "colorable imitation" of the patented design. This simplifies the test for infringement and shifts the burden of comparing the patented design to prior art to the accused infringer. The decision also cautions against describing a design patent's drawings with words, which could unduly emphasize particular features over the design as a whole. This ruling should reduce design patent litigation costs for patent holders and make summary judgment of infringement more likely.
SKGF_Advisory_Two Questions Every Wind Energy Company Should Ask Itself_2009SterneKessler
Before bringing a new wind turbine product to market, companies should ask two important questions: 1) Does someone hold a patent that could block sales of the product? and 2) Can the company's patents block competitors from selling similar products? To answer the first question, companies should thoroughly review their product and related patents to ensure freedom to operate without infringement. They should also consider pending patent applications that could issue as enforceable patents. To answer the second question, companies should seek patents on novel and non-obvious aspects of their product to create roadblocks for competitors. Conducting this analysis can help companies avoid infringement liability and protect their market position.
The document summarizes the February 24, 2006 hearing between NTP, RIM, and the US government over NTP's patent infringement claims against RIM regarding Blackberry technology. It outlines two possible scenarios for how the judge, James R. Spencer, may rule on damages and an injunction. The first scenario has Judge Spencer siding more with NTP, awarding them full damages and ultimately blocking Blackberry services. The second scenario favors RIM more, with lower initial damages and no service interruption. The authors believe the first outcome is more likely.
SKGF_Advisory_Strategies for Life Under the New USPTO Rules on Continuation a...SterneKessler
The document summarizes new rules from the USPTO regarding continuation and claims practice that take effect on November 1, 2007. Key points of the new rules include: limiting the number of claims to 5 independent and 25 total without an examination support document; limiting continuations and RCEs to two "as of right" per family; requiring commonly owned applications to be identified. The document provides strategies for dealing with the new rules such as using suggested restriction requirements and filing continuations serially after a parent is allowed.
SKGF_Advisory_SKGF Forms Stem Cell Task Force Advisory_2005SterneKessler
A law firm formed a Stem Cell Task Force in 2004 to stay up-to-date on legal and policy developments regarding stem cells and inform clients. The task force has published three pieces on stem cell patenting, including one on California's Proposition 71 and the stem cell patent landscape. Their latest publication discusses whether patent pools could help resolve stem cell patent issues.
SKGF_Advisory_Reexamination Practice with Concurrent District Court or USITC ...SterneKessler
This document discusses the interplay between patent litigation in federal courts or the International Trade Commission and concurrent reexamination proceedings involving the same patent before the US Patent and Trademark Office. It notes that these "parallel universes" operate with separate rules, standards, procedures, timelines and results. The increased use of reexamination as an alternative venue to challenge patent validity when district court litigation has been initiated is discussed. Key factors driving this include the USPTO's focus on making reexamination more efficient and changes in the legal landscape regarding patent validity and obviousness standards from Supreme Court cases. The impact of potential reexaminations is now commonly considered in nearly all patent litigation.
SKGF_Advisory_Real World Impacts of Reexamination Practice and Procedure_2008SterneKessler
This document discusses issues related to patent reexamination procedures and their impact on patent owners. It provides background on ex parte and inter partes reexamination procedures. It then discusses concerns about the low standard for instituting reexaminations, the impact of reexaminations on capital markets, and identifying the real party in interest in inter partes reexaminations. It proposes solutions such as increasing the standard for reexaminations involving previously litigated patents or previous reexams and keeping reexamination proceedings confidential until a final office action.
SKGF_Advisory_Preparing and Prosecuting a Patent that Holds up in Litigation_...SterneKessler
This document provides guidance on preparing and prosecuting a patent application to obtain a patent that will withstand litigation. It discusses considerations prior to filing such as conducting a prior art search, carefully drafting claims to avoid obvious errors or unnecessary limitations, and ascertaining inventorship. During prosecution, it recommends fully complying with the duty of disclosure and using interviews and narrowing amendments strategically. Post-issuance, it suggests using certificates of correction, reissue applications, and reexamination where needed to strengthen the patent. The overall goal is to obtain a valid, enforceable patent by addressing weaknesses before they can be exploited in litigation.
SKGF_Advisory_Living in a Post KSR World_2007SterneKessler
This document provides an overview of how the Supreme Court's 2007 decision in KSR International Co. v. Teleflex Inc. has impacted obviousness determinations at the Federal Circuit, district courts, and USPTO. Since KSR, the Federal Circuit has found inventions obvious in 6 out of 9 precedential decisions. While some language in opinions remains similar to pre-KSR cases, the standard for determining obviousness is less rigid, with motivation or reason to combine references no longer required to be explicit. District courts are more readily granting summary judgment of obviousness. The USPTO has also been impacted but specifics are still emerging.
SKGF_Advisory_Federal Circuit Issues Decision in TAFAS v. Doll_2009SterneKessler
The United States Court of Appeals for the Federal Circuit issued a decision in Tafas v. Doll regarding USPTO rules on claims, continuation applications, and Requests for Continuation Examination (RCEs). While the Federal Circuit found the rules to be procedural and within the USPTO's authority, it determined the rule limiting continuation filings to two was inconsistent with statute. The validity of the rules limiting claims and RCEs was not affirmed and was remanded for further consideration. The opinion was issued by a three-judge panel with disagreement on some aspects. The parties can request rehearing by the full panel of judges.
SKGF_Advisory_Stem Cells-Patent Pools to the Rescue_2005SterneKessler
Stem cell research faces challenges due to numerous existing and pending patents covering related technologies. A patent pool is proposed to consolidate these patents into a single license to streamline access for researchers and developers. A patent pool would integrate complementary patents and reduce costs by avoiding multiple licensing agreements. However, any patent pool must be carefully designed to avoid anti-competitive behaviors like restricting innovation. If properly structured, a stem cell patent pool could enable continued progress while respecting patent holders' rights.
SKGF_Advisory_Nanotechnology Practice News_2005SterneKessler
The law firm Sterne, Kessler, Goldstein & Fox provides an update on its growing nanotechnology practice. It has hired three new Ph.D. scientists - Dr. Barron, Dr. Lukas, and Dr. Tuminaro - to strengthen its technical expertise in areas like tissue engineering, protein microarrays, nanoporous materials, and solid state physics. It has also analyzed nanotechnology patent prosecution histories and plans to present preliminary results of its comprehensive study of all nanotube patents issued in 2004 at the 2005 NSTI conference.
SKGF_Presentation_The Supreme Courts Renewed Interest In IP_April 2007SterneKessler
The Supreme Court has recently taken a renewed interest in intellectual property cases, reviewing and reversing several Federal Circuit rulings over the past decade. This suggests the Supreme Court is unhappy with the Federal Circuit's handling of patent law and prefers flexibility over bright-line rules. There are indications the Supreme Court views IP law as more important today than in the past and wants to ensure consistency with how other types of cases are handled. The talk examines this growing tension between the two courts with implications for how patent cases may be decided going forward.
This document discusses intellectual property considerations for nanotechnology. It defines intellectual property and outlines patent, trademark, copyright and trade secret protections. It focuses on patent rights, describing the requirements to obtain a patent, the patent application process, and key stages from conception of an idea to patent issuance. Challenges in nanotechnology such as incomplete ideas and newness of the field are addressed. The importance of documentation, education of attorneys, broad claims, and leveraging the patent process are emphasized for obtaining strong nanotechnology patent rights.
SKGF_Presentation_Stem Cells The Patent Landscape_2005SterneKessler
1. Several patents exist related to stem cell research, including patents covering methods of culturing primordial germ cells and pluripotent embryonic stem cells.
2. The Wisconsin Alumni Research Foundation (WARF) owns patents related to human embryonic stem cells that are reportedly available for licensing.
3. WARF is asking for $100,000 upfront fee and $25,000 annual fee to license their patents for commercial use related to stem cell therapies.
The document summarizes the results of a 2004 study of 206 US patents issued that year containing "nanotube" in the claims, finding that the patents covered a wide range of technologies, took an average of 28 months to issue, and examinations showed relatively high allowance rates, suggesting less rigorous review by the Patent Office.
SKGF_Presentation_Nanotechnology IP Licensing Think Big, But Keep Your Feet O...SterneKessler
This document summarizes a presentation on nanotechnology intellectual property licensing. It discusses how the USPTO is handling nanotechnology patents, noting the disruptive and pervasive nature of nanotechnology. It outlines challenges in obtaining patent protection for nanotechnology inventions due to issues like enablement, inherency, and breadth of claims. The document also discusses considerations for nanotechnology licensing agreements, including ownership issues, license income structures, and performance requirements.
Marvin C. Guthrie presented at the International Engineering Consortium NanoEngineering World Forum on June 23, 2003. The presentation discussed intellectual property strategies for transferring technology depending on whether you are from academia, industry or venture capital. It also covered issues like funding source encumbrances, acquiring technology through assignments and licenses, exclusivity in licenses, and considerations in licensing agreements like maintenance of IP and enforcement.
Focus on Pharma: Creating, Protecting & Enforcing High-Value IP AssetsSterneKessler
A two-day conference held by Sterne, Kessler, Goldstein & Fox P.L.L.C., which focused on on recent trends in substantive case law, their impact on patent prosecution and examination, and implications regarding the enforcement of patents in the pharmaceutical and biopharmaceutical industry.
This document summarizes a USPTO Bio/Chem/Pharma Customer Partnership meeting in September 2006. About 100 people attended in person and 40 attended virtually. Key topics discussed included recent changes to restriction practice, data on restriction petition outcomes, new accelerated examination rules, the examination of bioinformatics cases, and upcoming proposed rule changes regarding claims, continuations, IDS practice and Markush claims. Speakers from various technology centers and art units provided updates in their areas. Attendees engaged in discussion and questions.
SKGF_Advisory_US Design Patents Strengthened by Recent Federal Circuit Ruling...SterneKessler
The Federal Circuit issued a decision strengthening US design patents. It threw out the "point of novelty" test for infringement and returned to a test of whether the accused design is "substantially the same as" or a "colorable imitation" of the patented design. This simplifies the test for infringement and shifts the burden of comparing the patented design to prior art to the accused infringer. The decision also cautions against describing a design patent's drawings with words, which could unduly emphasize particular features over the design as a whole. This ruling should reduce design patent litigation costs for patent holders and make summary judgment of infringement more likely.
SKGF_Advisory_Two Questions Every Wind Energy Company Should Ask Itself_2009SterneKessler
Before bringing a new wind turbine product to market, companies should ask two important questions: 1) Does someone hold a patent that could block sales of the product? and 2) Can the company's patents block competitors from selling similar products? To answer the first question, companies should thoroughly review their product and related patents to ensure freedom to operate without infringement. They should also consider pending patent applications that could issue as enforceable patents. To answer the second question, companies should seek patents on novel and non-obvious aspects of their product to create roadblocks for competitors. Conducting this analysis can help companies avoid infringement liability and protect their market position.
The document summarizes the February 24, 2006 hearing between NTP, RIM, and the US government over NTP's patent infringement claims against RIM regarding Blackberry technology. It outlines two possible scenarios for how the judge, James R. Spencer, may rule on damages and an injunction. The first scenario has Judge Spencer siding more with NTP, awarding them full damages and ultimately blocking Blackberry services. The second scenario favors RIM more, with lower initial damages and no service interruption. The authors believe the first outcome is more likely.
SKGF_Advisory_Strategies for Life Under the New USPTO Rules on Continuation a...SterneKessler
The document summarizes new rules from the USPTO regarding continuation and claims practice that take effect on November 1, 2007. Key points of the new rules include: limiting the number of claims to 5 independent and 25 total without an examination support document; limiting continuations and RCEs to two "as of right" per family; requiring commonly owned applications to be identified. The document provides strategies for dealing with the new rules such as using suggested restriction requirements and filing continuations serially after a parent is allowed.
SKGF_Advisory_SKGF Forms Stem Cell Task Force Advisory_2005SterneKessler
A law firm formed a Stem Cell Task Force in 2004 to stay up-to-date on legal and policy developments regarding stem cells and inform clients. The task force has published three pieces on stem cell patenting, including one on California's Proposition 71 and the stem cell patent landscape. Their latest publication discusses whether patent pools could help resolve stem cell patent issues.
SKGF_Advisory_Reexamination Practice with Concurrent District Court or USITC ...SterneKessler
This document discusses the interplay between patent litigation in federal courts or the International Trade Commission and concurrent reexamination proceedings involving the same patent before the US Patent and Trademark Office. It notes that these "parallel universes" operate with separate rules, standards, procedures, timelines and results. The increased use of reexamination as an alternative venue to challenge patent validity when district court litigation has been initiated is discussed. Key factors driving this include the USPTO's focus on making reexamination more efficient and changes in the legal landscape regarding patent validity and obviousness standards from Supreme Court cases. The impact of potential reexaminations is now commonly considered in nearly all patent litigation.
SKGF_Advisory_Real World Impacts of Reexamination Practice and Procedure_2008SterneKessler
This document discusses issues related to patent reexamination procedures and their impact on patent owners. It provides background on ex parte and inter partes reexamination procedures. It then discusses concerns about the low standard for instituting reexaminations, the impact of reexaminations on capital markets, and identifying the real party in interest in inter partes reexaminations. It proposes solutions such as increasing the standard for reexaminations involving previously litigated patents or previous reexams and keeping reexamination proceedings confidential until a final office action.
SKGF_Advisory_Preparing and Prosecuting a Patent that Holds up in Litigation_...SterneKessler
This document provides guidance on preparing and prosecuting a patent application to obtain a patent that will withstand litigation. It discusses considerations prior to filing such as conducting a prior art search, carefully drafting claims to avoid obvious errors or unnecessary limitations, and ascertaining inventorship. During prosecution, it recommends fully complying with the duty of disclosure and using interviews and narrowing amendments strategically. Post-issuance, it suggests using certificates of correction, reissue applications, and reexamination where needed to strengthen the patent. The overall goal is to obtain a valid, enforceable patent by addressing weaknesses before they can be exploited in litigation.
SKGF_Advisory_Living in a Post KSR World_2007SterneKessler
This document provides an overview of how the Supreme Court's 2007 decision in KSR International Co. v. Teleflex Inc. has impacted obviousness determinations at the Federal Circuit, district courts, and USPTO. Since KSR, the Federal Circuit has found inventions obvious in 6 out of 9 precedential decisions. While some language in opinions remains similar to pre-KSR cases, the standard for determining obviousness is less rigid, with motivation or reason to combine references no longer required to be explicit. District courts are more readily granting summary judgment of obviousness. The USPTO has also been impacted but specifics are still emerging.
SKGF_Advisory_Federal Circuit Issues Decision in TAFAS v. Doll_2009SterneKessler
The United States Court of Appeals for the Federal Circuit issued a decision in Tafas v. Doll regarding USPTO rules on claims, continuation applications, and Requests for Continuation Examination (RCEs). While the Federal Circuit found the rules to be procedural and within the USPTO's authority, it determined the rule limiting continuation filings to two was inconsistent with statute. The validity of the rules limiting claims and RCEs was not affirmed and was remanded for further consideration. The opinion was issued by a three-judge panel with disagreement on some aspects. The parties can request rehearing by the full panel of judges.
SKGF_Advisory_Stem Cells-Patent Pools to the Rescue_2005SterneKessler
Stem cell research faces challenges due to numerous existing and pending patents covering related technologies. A patent pool is proposed to consolidate these patents into a single license to streamline access for researchers and developers. A patent pool would integrate complementary patents and reduce costs by avoiding multiple licensing agreements. However, any patent pool must be carefully designed to avoid anti-competitive behaviors like restricting innovation. If properly structured, a stem cell patent pool could enable continued progress while respecting patent holders' rights.
SKGF_Advisory_Nanotechnology Practice News_2005SterneKessler
The law firm Sterne, Kessler, Goldstein & Fox provides an update on its growing nanotechnology practice. It has hired three new Ph.D. scientists - Dr. Barron, Dr. Lukas, and Dr. Tuminaro - to strengthen its technical expertise in areas like tissue engineering, protein microarrays, nanoporous materials, and solid state physics. It has also analyzed nanotechnology patent prosecution histories and plans to present preliminary results of its comprehensive study of all nanotube patents issued in 2004 at the 2005 NSTI conference.
SKGF_Presentation_The Supreme Courts Renewed Interest In IP_April 2007SterneKessler
The Supreme Court has recently taken a renewed interest in intellectual property cases, reviewing and reversing several Federal Circuit rulings over the past decade. This suggests the Supreme Court is unhappy with the Federal Circuit's handling of patent law and prefers flexibility over bright-line rules. There are indications the Supreme Court views IP law as more important today than in the past and wants to ensure consistency with how other types of cases are handled. The talk examines this growing tension between the two courts with implications for how patent cases may be decided going forward.
This document discusses intellectual property considerations for nanotechnology. It defines intellectual property and outlines patent, trademark, copyright and trade secret protections. It focuses on patent rights, describing the requirements to obtain a patent, the patent application process, and key stages from conception of an idea to patent issuance. Challenges in nanotechnology such as incomplete ideas and newness of the field are addressed. The importance of documentation, education of attorneys, broad claims, and leveraging the patent process are emphasized for obtaining strong nanotechnology patent rights.
SKGF_Presentation_Stem Cells The Patent Landscape_2005SterneKessler
1. Several patents exist related to stem cell research, including patents covering methods of culturing primordial germ cells and pluripotent embryonic stem cells.
2. The Wisconsin Alumni Research Foundation (WARF) owns patents related to human embryonic stem cells that are reportedly available for licensing.
3. WARF is asking for $100,000 upfront fee and $25,000 annual fee to license their patents for commercial use related to stem cell therapies.
The document summarizes the results of a 2004 study of 206 US patents issued that year containing "nanotube" in the claims, finding that the patents covered a wide range of technologies, took an average of 28 months to issue, and examinations showed relatively high allowance rates, suggesting less rigorous review by the Patent Office.
SKGF_Presentation_Nanotechnology IP Licensing Think Big, But Keep Your Feet O...SterneKessler
This document summarizes a presentation on nanotechnology intellectual property licensing. It discusses how the USPTO is handling nanotechnology patents, noting the disruptive and pervasive nature of nanotechnology. It outlines challenges in obtaining patent protection for nanotechnology inventions due to issues like enablement, inherency, and breadth of claims. The document also discusses considerations for nanotechnology licensing agreements, including ownership issues, license income structures, and performance requirements.
Marvin C. Guthrie presented at the International Engineering Consortium NanoEngineering World Forum on June 23, 2003. The presentation discussed intellectual property strategies for transferring technology depending on whether you are from academia, industry or venture capital. It also covered issues like funding source encumbrances, acquiring technology through assignments and licenses, exclusivity in licenses, and considerations in licensing agreements like maintenance of IP and enforcement.
SKGF_Presentation_USPTO Patent Examination Reform and Proposed Rule Changes-2006
1. USPTO Patent Examination Reform
and
Proposed Rule Changes
Michael Messinger, Esq.
February 27, 2006
504895_1.ppt
2. USPTO Initiatives
• Overview
• Backdrop at the USPTO
• Proposed Rules Changes
• Other Initiatives
2
3. USPTO Initiatives
• Changes on the Ground Already
New Building
Hired 1000 new Examiners in 2005
Central Re-exam Unit Formed July 2005
Second-Layer Review – extended Office wide
Software Prior Art
Patent Academy Changes
Examiner re-certification
Telecommuting/Remote Sites/Regional Offices
3
4. USPTO Initiatives
• Changes on the Ground Already
Reduced Allowance rate
58.7% Allowance rate Office Wide (down from
traditional 80%+ rate)
11% Allowance rate in business methods
Reduced Patent Allowance error rate
In FY 2005, 4.55% error rate
Increased Pendency
But dramatic reduction in pendency for cases on appeal
4
5. Problems from PTO Perspective:
• Pendency
• Keeping Up with Growth
• Quality
• Past Solutions Failed
5
6. First Action Pendency by Art Areas
Pendency Pendency
High Pendency Art Areas Low Pendency Art Areas
1 1
(months)
(months)
1640 – Immunology, Receptor/
1620 – Heterocyclic Compounds
27.7 16.9
Ligands, Cytokines, Recombinant
and Uses
Hormones, and Molecular Biology
1743 – Analytic Chemistry & Wave
30.8 1752 – Radiation Imagery 12.1
Energy
2123 – Simulation and Modeling, 2125 – Manufacturing Control
39.7 20.0
Emulation of Computer Systems and Chemical/
Components Mechanical/Electrical Control
2617 – Interactive Video 2651 – Dynamic Information
50.4 16.1
Distribution Storage & Retrieval
2836 – Control Circuits 24.3 2833 – Electrical Connectors 8.8
3628 – Finance & Banking,
52.1 3612 – Land Vehicles 12.0
Accounting
3731 – Surgery: Cutting, Clamping,
30.9 3723 – Tools & Metal Working 10.9
Suturing
1
“Average 1st action pendency” is the average age from filing to first action for a newly filed application, completed during October-December 2005.
6
7. Inventory by Art Examples
Months of Months of
High Inventory Art Areas Low Inventory Art Areas
Inventory* Inventory*
1614, 1615, and 1617 – Drugs,
38-51 1620 – Organic Chemistry 15
Bio-affecting and Body
Treatment
1734 – Adhesive Bonding and
1753 – Radiation Imagery 34 10
Coating Apparatus
2125 – Manufacturing Control
2127 – Computer Task
46 10
Systems and Chemical/
Management
Mechanical/Electrical Control
2611 – Interactive Video 2651, 2653 – Information
111 12
Distribution Storage and Retrieval
2836 – Control Circuits 22 2831 – Electrical Conductors 8
3620 – Business Methods 25-130 3651 – Conveying 12
3731 and 3737 – Medical
3742 – Thermal and
Instruments, Diagnostic 38-47 8
Combustion Technology
Equipment
*The number of months it would take to reach a first action on the merits (e.g., an action addressing patentability issues) on a new application filed in
July 2005 at today’s production rate. Today’s production rate means that there are no changes in production due to hiring, attrition, changes to
examination processing or examination efficiencies, and that applications are taken up in the order of filing in the given art unit/area. Of course,
USPTO is taking aggressive steps to ensure changes that will significantly lower the inventory rates in high-inventory art areas.
7
8. TC Application Inventory
1600 1700 2100 2600 2800 3600 3700 Total* Design
New
Applications1 55,402 63,923 71,778 97,380 77,651 56,738 65,005 508,878 18,451
9/30/2004
New 115,58
Applications1 62,644 72,697 76,529 94,425 70,354 83,225 586,580 24,534
5
9/30/2005
Overall
102,44 138,82 101,09
Pending
95,006 105,447 137,458 108,039 809,323 27,599
Applications2 0 2 7
9/30/2004
Overall
107,64 117,72 167,72 117,04
Pending
120,767 159,687 130,168 932,300 38,104
Applications2 7 8 1 5
9/30/2005
“New Application inventory” is the number of new applications designated or assigned to a technology center awaiting a first action.
1
“Overall Pending Application inventory” is the total number of applications designated or assigned to a technology center in an active status. Includes
2
new applications; rejected awaiting response; amended; under appeal or interference; suspended; reexams and allowed applications awaiting grant
publication.
*Total inventory includes applications not assigned to a particular TC, awaiting processing either pre- or post-examination.
8
9. Technology Centers Rework* Statistics
FY 2002 FY 2003 FY 2004 FY 2005
TC % FAOM % FAOM % FAOM % FAOM
Summary Rework Rework Rework Rework
1600 36.4% 39.7% 40.3% 42.4%
1700 25.2% 26.9% 27.1% 28.0%
2100 23.9% 24.0% 24.6% 28.2%
2600 24.8% 24.2% 24.3% 25.4%
2800 19.1% 22.0% 24.9% 24.1%
3600 17.7% 21.2% 23.2% 28.5%
3700 22.2% 25.1% 24.0% 28.1%
UPR 23.2% 25.3% 26.1% 28.3%
* Rework first actions are those actions that are in a Continuing (CONs and CIPs), RCE, CPA or 129(a)
applications (excludes Divisionals).
9
17. USPTO Initiatives
• Rule Making Proposals
– Limits to Continuation Practice (comments
due May 3, 2006)
– Limits to Claim Examination (comments due
May 3, 2006)
17
18. Goal of Proposed Rule Changes
• Proposed Rule Changes aim to free up
Examiner resources now spent on re-work and
initial claims so more time can be spent on
initial examination of first time cases in
backlog.
18
19. Limitation on Continuations/RCEs
• The key provisions in the proposed change to
limit continuations/RCEs are:
– Only one continuation or RCE as a matter of right
allowed.
– Additional continuations or RCE available only if
special showing is made. This showing is
expected to be fairly strict. Applicant must show
that amendment, argument or evidence “could not
have been” presented earlier.
19
20. Special rules for Divisionals/CIPs include:
• No voluntary divisionals allowed.
• Divisional can be filed only when Examiner
has made a restriction requirement.
• Divisional may only claim benefit of a single
prior-filed non-provisional application.
20
21. Special rules for Divisionals/CIPs (cont’d)
• CIPs have an identification requirement:
– Applicants must identify what claims are
supported by parent disclosure
– Claims not identified are only given filing date of
CIP
– Continuation of CIP permitted but only entitled to
benefit of CIP
• Practical result is only claims drawn to “new
matter” of CIP will be pursued in continuation
of CIP.
21
22. Limits to Double Patenting
• Key provisions are:
– Identification requirement. Applicants must identify other applications
or patents having common inventor, common assignee, and filed within
two months of each other (taking into account priority/benefit claims).
– Rebuttable presumption of double patenting is created if identified
applications/patents have same effective filing date and substantially
overlapping disclosure.
– Applicant can overcome presumption by showing claims are patentably
distinct; or filing a terminal disclaimer AND explaining why patentably
indistinct claims in different applications should be maintained.
– USPTO can require merger or cancellation of patentably indistinct
claims in one application or across multiple applications where at least
one common inventor and commonly-owned, unless applicant can
provide a good and sufficient reason.
22
23. Representative Claim Examination
• Key provisions are:
– Representative Claim Designation. Applicant must designate up to 10
claims for initial examination. Full initial examination conducted for
designated representative claims only. Only when representative
claims are allowed are remaining dependent claims examined for 35
U.S.C. §101 and §112 compliance.
– Examination Support Document. Designation of more than 10 claims
is only possible if Applicant also provides an Examination Support
document. Examination Support document must: identify scope of
search conducted by Applicant (including US and Intl patents, non-
patent literature), identify all limitations of representative claims that
are disclosed by cited references, explain how all representative claims
are patentable over the cited references, show support in specification
for each representative claim, and identify utility for each independent
claim.
– Retroactivity. Will apply to pending applications that have not yet
received first action on merits.
23
24. Representative Claim Examination (cont’d)
• Normal pattern will be – Applicant identifies up
to 10 representative claims for initial
examination:
– must include all independent claims
– if less than 10 independent claims, then can
designate dependent claims up to a total of 10
(indep and dep.)
24
25. Election of Claims – Example 1
1 6 7 10 11 12
= independent claim
Red = elected claim
2 4
8 9 13 14 Black = non-elected claim
3 5
All independent claims must be elected.
The election of claim 3 is improper. An elected dependent claim must depend
from another elected claim. Applicant can choose to re-write claim 3 to depend from
1, or also elect claim 2 to be examined.
25
26. Election of Claims – Example 10
An applicant files an application with claims to 3 distinct
inventions. The application is filed with 30 claims: 3
independent claims and 27 dependent claims.
If applicant designates all 27 dependent claims for initial examination,
the application will have 30 representative claims. The applicant
must:
• submit an examination support document covering the 30
representative claims;
• reduce the number of representative claims to 10 or fewer by
canceling independent claims, rescinding the designating of
dependent claims for initial examination, or a combination thereof;
and/or
• reduce the number of representative claims to 10 or fewer by
suggesting a requirement for restriction and election w/out traverse of
such representative claims.
26
27. Continuations
Benefit Claims under 35 USC 120, 121, or 365(c)
One RCE, Continuation, or CIP Permitted
#1 #2 #3
Nonprovisional
Provisional Applicant may file:
Application
Application an RCE, or
claiming the a continuation or a CIP
benefit of the application, claiming a benefit
provisional under 35 USC 120, 121 or 365(c)
application,
35 USC 119(e)
27
28. Continuations
Benefit Claims under 35 USC 120, 121, or 365(c)
Divisional Applications Can Only Claim Benefit of One
Prior Nonprovisional Application That Was Subject to a
Restriction or Unity of Invention Requirement
Restriction made #2 #3
#1
in Application #1
Applicant may file
Nonprovisional Applicant
Divisional Applications claiming only the
Application elected invention
benefit of application #1 and the claims
with claims to A and canceled
must be directed non-elected inventions
inventions A, claims directed
in application #1
B, and C to B, and C
28
29. Continuations
Benefit Claims under 35 USC 120, 121, or 365(c)
One Continuing Filing after a Divisional Permitted
Restriction made
in Application #2 #3
#2
#4
#1
Provisional Nonprovisional Divisional Applicant may file:
Application Application claiming the Application (as a single RCE, or
benefit of the defined in proposed continuation or CIP
provisional application, rule) to non-elected application of the divisional
35 USC 119(e) invention application
29
30. Continuations
Benefit Claims under 35 USC 120, 121, or 365(c)
Second Continuing Filing Requires Petition &
Showing That the Amendment, Argument, or
Evidence Could Not Have Been Earlier
Submitted
#1 #2 #3 #4
Provisional Nonprovisional A first Applicant may file a second
Application Application continuing or subsequent RCE or
claiming the application or continuing application w/ a
benefit of the an RCE
petition and showing
provisional
application
30
31. Continuations – Example 1
Scenario: Applicant files application #1 with 65 claims. The USPTO requires
restriction between the following groups:
Invention 1 - 15 claims; 3 independent + 12 dependent claims
I.
Invention 2 - 30 claims; 5 independent + 25 dependent claims
II.
Invention 3 - 20 claims; 1 independent + 19 dependent claims
III.
Applicant may file two divisional applications, one each for inventions 2 and 3.
But, both will need to be filed during the pendency of application #1 in
order to be entitled to claim the benefit of application #1’s filing date.
If divisional #3 is filed during the pendency of divisional #2, but not
during pendency of application #1, it will only be entitled to the filing
date of divisional #2.
31
32. Continuations – Example 2
Scenario: Applicant files application #1 claiming only 1 invention. Later, applicant
files application #2 with the same disclosure but claims direction to a different
invention. In application #2, the applicant claims the priority of application #1’s
filing date.
This is permitted, but application #2 will be treated as the one continuation of
application #1 allowed as a matter of right.
Therefore, neither applications #1 or #2 can have any additional RCEs or
continuations absent a petition.
Also, as both applications have the same effective filing date, there will be
rebuttable presumption of double patenting. The applicant will need to file a
terminal disclaimer or argue persuasively that the claims are patentably
distinct.
32
33. Examples of a Showing for Filing a
Second Continuing Application
Example 1: In a continuation application,
• An interference is declared in an application
containing both claims corresponding to the
count(s) and claims not corresponding to the
count(s), and
• The APJ suggests that the claims not
corresponding to the count(s) be canceled from
the application in interference and pursued in a
separate application.
33
34. Examples of a Showing for Filing a
Second Continuing Application
Example 2: In a continuation application,
• Data necessary to support a showing of
unexpected results just became available to
overcome a final rejection under 35 U.S.C.
103, and
• The data is the result of a lengthy
experimentation that was started after
applicant received the rejection for the first
time.
34
35. Examples of a Showing for Filing a Second
Continuing Application
Example 3: In a continuation application,
• The final rejection contains a new ground of
rejection that could not have been
anticipated by the applicant, and
• The applicant seeks to submit evidence
which could not have been submitted earlier
to overcome this new rejection.
35
36. Examples of Unacceptable Showing for Filing
a Second Continuing Application
Example 1:
• An argument that a final rejection in one of
the prior applications was premature.
• Applicant should address the propriety of the
final rejection during prosecution of the prior
application, and not collaterally in a petition
for a continuation application.
36
37. Examples of Unacceptable Showing for Filing a
Second Continuing Application
Example 2:
• An argument that an amendment after final
rejection should have been entered in the
prior application.
• Applicant should address the non-entry in
the prior application, and not collaterally in a
petition for a continuation application.
37
38. IMPACT OF
PROPOSED RULE CHANGES ON SMALL
BUSINESSES
38
40. EXTRACT VALUE
INCREASED COSTS
$970 $3,000
$895
$14,415 $3,378
RCE / CON.
$12,665 $2,937
1
First Office Final Office
NON-PROVISIONAL $10,624
Action Action
● special $ 9,369
showing
APPEAL
PENDENCY
THE filed filed
4 years
INVENTION 1st Final
10 ● retroactive OA OA
ALLOWANCE
$30,000 Examination Support Document $5,000 $1,722
$1,722
● identification
● rebuttable presumption
● Rigid
● terminal disclaimer + showing
● Loss of Rights
● PTO merger / cancel right
● Increase Work
● Undercut Value DIVI- RCE /
APPEAL
SIONAL CON.
● More Contentious win-lose predicaments
● not
$6,000
matter
(3-way)
ALLOWANCE
of right
● Continuation / RCE limit: 1 absent special showing
● Divisional: not a matter of right
RCE or
APPEAL
● CIP: identification, continuation limited to new matter C-I-P
CON.
● Double Patenting: identification, rebuttable presumption,
terminal disclaimer plus showing, PTO merger / cancel right
● Claims: 10, retroactive ● identifi-
$3,000
ALLOWANCE
cation
40
41. Problems from PTO Perspective:
• Pendency: Time to first Office Action – e.g., 50
months in Interactive Video.
• Keeping Up: Growth in Filings – 8.1% overall FY
2005, 21% wireless communication; Avg. number of
claims at filing rose from 15 to 23 between 1990-
2005; 28% of First Office Actions issued were re-
work after one or more RCE/CON, but 83% of CON
were a first CON.
• Quality: Rise in claims and re-work – burdensome –
reduces examination quality.
• Past Solutions Failed: Hiring alone not enough,
Backlog grows.
41
42. Goal of Proposed Rule Changes
• Proposed Rule Changes aim to free up
Examiner resources now spent on re-work and
initial claims so more time can be spent on
initial examination of first time cases in
backlog.
42
43. Small Business Perspective
• Proposed Rule changes-
– Disproportionately impact individual inventors, start-ups, emerging
growth companies, and pioneering or active innovators.
– Provide less protection when most needed by small businesses
– Create more contentious process, more complex.
– Drive up cost of application preparation and prosecution throughout
process.
– Increase risk and reduce value of patent portfolios - more vulnerable to
latecomer, free riders.
– Reward lawyering not innovation.
– Exacerbate PTO pendency problem – shifts Examiner resources to
address procedural impediments not merits of claims sought
43
44. Small Business Perspective (cont’d)
• Time to Patent Issuance is the relevant pendency metric.
• Approximately 22 percent of all U.S. origin patents in 2000 claimed
small entity status including 15% individual inventor, 6% small
business and 1% non-profit organization.
• Pendency needs vary - one size fit all makes no sense -
– Inventions in basic R&D or with long development cycle (bio)
can wait longer.
– Inventions by small businesses need shorter time to patent.
– Fast moving technologies (Internet/wireless) need shorter time
to patent for some matters.
– For leading inventions short time to patent matters. For follow-
on improvements and continuations longer pendency is often
tolerable, but ability to introduce new claims critical.
44
45. Small Business Perspective (cont’d)
• Burden sharing – well-defined search burden can be
accommodated, but written comments burdensome
for small businesses, drive up cost, and risk to
portfolio.
• Quality – PTO is right - a quality issued patent is key,
quality first office action important; Examiner as lone
wolf unworkable model. Need to leverage interview
and negotiation time better - not written record of
prosecution. Written reasons for allowance are
better use of Examiners’ time than Office Action
remarks.
• Examiner skills: More technical industry experience
needed.
45
46. Limits on Continuation Practice
One RCE/Continuation absent special showing
• Direct Impact:
– more contentious examination process, all innovation
cannot be claimed, drives up cost at each stage of
prosecution, reduces ability of patent system to promote
useful arts – outnumbered innovator cannot thwart free
riding, Monday morning quarterbacking, and wordsmith
design arounds by latecomers up and down value chain.
• Unintended Consequence:
– reduces Examiner morale – reduces large territory of deal
making, increases work of Examiner - length and #
interviews , traversals to final rejection, time spent
reviewing special showing, and re-opening prosecution
from Board of Appeals (BPAI).
46
47. Limits on Double Patenting Practice
Identification requirement and special showing
• Direct Impact:
– Increases cost and complexity.
• Unintended Consequence:
– Hurts pioneering inventors and start-ups most. Works
against continued investment and development of most
important inventions – identified as patentable. More work
for examiners to review identification requirement, special
showing on patentably distinct, and contentions over
merger/cancellation, attempts to solve a problem that
does not exist, current system with duty of disclosure and
Terminal Disclaimer practice works.
47
48. Limits on Claims Practice
Only 10 claims initially examined absent submission of examination
support documentation, retroactive to pending cases
• Direct Impact: Increases complexity identifying/ tracking
designated claims at each stage of examination; leaves
innovation unprotected – ten sentences too little, retroactivity
unfair since currently pending claims drafted without
consideration of ten claim designation, requires immediate
expense to review claim strategy of all pending matters
(600,000 cases).
• Unintended Consequence: More work for Examiner,
undercuts efficiency of a complete first office Action,
increases likelihood of new work after first action when
different designated claims are selected or considered for first
time at allowance; impact compounded by limits on
continuation to make it likely that all innovation cannot be
claimed, reduces ability of patent system to promote useful
arts x
48
49. Limits on Divisional Practice
• No divisionals allowed as a matter of right – only in
response to Examiner initiated restriction, must be
co-pending with first filed parent.
• Direct Impact:
– Applicants more vulnerable to inappropriate Examiner multi-
way restrictions, increased cost to file multiple divisional during
life of parent.
• Unintended Consequence
– More work for Examiner to consider traversals to restriction
requirements, more work to consider Applicants’ requests for
restrictions to create opportunities not provided under proposed
limits to continuation practice.
49
50. Limits on CIP (continuation-in-part) Practice
Continuation of CIPs limited to claim new subject
matter in CIP, and CIP claims must identify
support in parent.
• Direct Impact: Increases cost and complexity
of CIP filing and examination
• Unintended Consequence: More work for
Examiner to ensure support identification
requirement met and new claims directed to
new subject matter only in continuing CIPs.
50
51. Solutions with Better Aim,
Better Results
• Applicants select level of pendency service – deferred examination,
regular examination, or accelerated examination.
• Remove 2-year limitation on broadening reissue.
• Permit wider interview practice and negotiation.
• Encourage more written analysis by Examiner at Allowance less during
active examination/ negotiation.
• Shifting search burden workable for Applicants and Examiner – require
only that Applicants describe scope of search not comments on particular
references.
• Increase fees for successive continuations/RCEs.
• Automatic deferred examination for successive continuations/RCEs
absent special fee or request.
• Reduce credit given to Examiner for work on successive
continuations/RCEs.
• Increase credit given to Examiner for interviews.
• Increase credit given to Examiner for successful focused Examination
51
52. USPTO Initiatives
• Other Initiatives
– Web-based electronic filing (EFS-web) – in beta – to be
released March 17, 2006
– New 5-yr Strategic plan for 2007-2012 underway
– Interim Guidelines on Eligible Subject Matter (comments
due June 2006)
– Accelerated 12 month Examination
– IDS Practice/Rule 1.56
– Limits on Markush practice
– Interviews before first Office Action
– Community Patent Review
52
53. The End
Credits: Several slides and statistical data taken from
presentations by John Doll and James Toupin of USPTO and
made available to public in February 2006.
53