Compulsory licensing is when a government authorizes a party other than the patent owner to produce the patented product or process, without the patent owner's consent.
Landmark case of Compulsory Licensing in IndiaKIRAN PATANGEThis document summarizes a landmark case in India involving the granting of a compulsory license for the cancer drug Sorafenib, marketed by Bayer as Nexavar. The key points are:
1) In 2012, Natco Pharma received a compulsory license from the Indian patent controller to manufacture and sell a generic version of Sorafenib, after Bayer refused to grant it a voluntary license.
2) The patent controller ruled in favor of Natco based on the grounds that the drug was not reasonably affordable or adequately available to the public in India. Bayer was charging over 45 times India's annual per capita income for the drug.
3) The compulsory license set the royalty rate
Patent war caseStudent Placement Coordinator,N.S.E.C Kolkata.The document summarizes two key patent cases in India - Novartis AG's plea seeking patent protection for its cancer drug Glivec, which was dismissed, and Natco Pharma's compulsory license application for the cancer drug Nexavar, which was granted. The Novartis ruling confirmed that slight modifications alone do not warrant patents under Indian law. The Nexavar ruling allowed Natco to sell cheaper copies of Nexavar, requiring it to pay Bayer royalties and supply some free doses annually. These rulings make life-saving drugs more affordable in India by allowing generics, though multinational companies argue they could reduce pharmaceutical investment and innovation.
CL PPTGunsaheb SinghThe document discusses compulsory licensing under Indian patent law. It provides context on what patents are, their purpose, and requirements for patentability. It then outlines key aspects of the Indian Patents Act of 1970 and amendments, including provisions for compulsory licensing. The grounds and process for obtaining a compulsory license are explained. It also summarizes a key legal precedent where Natco Pharma was granted a compulsory license for Bayer's anti-cancer drug Nexavar. The decision analyzed whether reasonable requirements were met, affordable pricing, and local working of the invention. The controller ultimately granted the license with price and royalty conditions.
Compulsory licenseAnubhav Mehracurrent scenario of patent act : compulsory license
article from indian journal of pharmaceutical education and research
compulsory license: natco vs bayer caseHelal Uddin MullahThis document provides an overview of the case of Natco Pharma Ltd. vs Bayer regarding the granting of the first ever compulsory license for a pharmaceutical patent in India. It discusses the key considerations and timeline of the case, including Natco's application for a compulsory license to produce the cancer drug Nexavar at an affordable price after Bayer refused to provide a voluntary license or lower the price. The document summarizes the Indian Patent Act provisions for compulsory licensing and the IPAB verdict upholding the license grant with a slightly increased royalty rate for Natco. It also outlines some of the effects on access to medicines and potential solutions.
Compulsory license of DrugsMahdy OsmanThis document discusses compulsory licensing of drugs under the TRIPS agreement. It defines compulsory licensing as allowing a government to produce a patented drug without the patent owner's consent. The Doha Declaration clarified that compulsory licensing can be used in cases of national emergency, non-commercial public use, and discriminatory pricing or refusal to supply drugs. Examples are given of countries that have issued compulsory licenses, including Egypt issuing one for Viagra and Thailand issuing them for several cancer drugs. Conditions for using compulsory licensing include attempting to obtain a voluntary license first and providing adequate remuneration to the patent holder.
Bayer vs Natco CaseManu DhunnaThe 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.
Patent fights in pharmaceutical sectorNitin PatelThis document discusses several patent cases in India between foreign pharmaceutical companies and Indian generic drug manufacturers. It summarizes key patent cases such as Novartis vs. India regarding Glivec, Bayer vs. Natco regarding Nexavar, Roche vs. Cipla regarding Tarceva. It also discusses India's patent laws including sections 3(d) and compulsory licensing. Many foreign drug patents were revoked by Indian courts based on lack of innovation or in the interest of public health and making medicines more affordable in India. The document supports India's stance on promoting generic competition and ensuring access to healthcare.
Compulsory licensing by surendraAnumulaSurendraThis document discusses compulsory licensing of patents in India. Compulsory licensing allows the government to grant a license to a third party to produce a patented product or use a patented process without the consent of the patent holder. The objectives are to reward patent holders while also making patented pharmaceutical products available to the public at affordable prices. Section 84 of the Indian Patent Act lays out the conditions for granting compulsory licenses, such as if the patented invention is not available to the public at a reasonable price. The first compulsory license granted in India was for the cancer drug Nexavar, allowing generic manufacturer Natco to sell a version at a much lower price than the branded version from Bayer.
Patent Overview in Novartis Case pptBizand LegisHuman rights and Patent Overview in Novartis Case power point presentation prepared by Anu B, Legal Intern published by Biz and Legis law firm.
Pharmaceutical patents in india – compulsory licensing, health emergency & af...Rahul DevPharmaceutical patents in india – compulsory licensing, health emergency & affordable healthcare – patent laws in india
pharmaceutical patenting in india, product patent in pharma, india pharmaceutical patent law, pharmaceutical patent cliff, pharmaceutical patent litigation, pharmaceutical patent lawyer, pharmaceutical patent expiry, pharmaceutical patent length, pharmaceutical patent expirations
Case analysis novartis vs union of indiaMohit BajajNovartis challenged the rejection of its patent application for the cancer drug Gleevec in India. The Madras Patent Office rejected the application on the grounds that Gleevec was merely a new salt form of the existing drug imatinib, and did not demonstrate enhanced efficacy as required by Section 3(d) of India's Patents Act. Novartis filed a legal challenge arguing that Section 3(d) violated international trade agreements and India's constitution. The court upheld Section 3(d) as compliant with trade rules and not arbitrary, finding that salt forms with modest improvements did not meet the standard of invention required for patents. The court also found it had jurisdiction to review compliance of domestic laws with international treaties.
Pharmaceutical patent Dr. Amit Gangwal Jain (MPharm., PhD.)Dr. amit gangwal ka pharmaceutical patent presentation
highly exhaustive and updated ppt on pharmaceutical patents, a must watch by all those concerned with the same.
Compulsory licensing (patents)Kumar Saurav Prasadcompulsory licensing of patents in India how to get compulsory licensing in India, procedure, rights involved, act and sections,limitation of compulsory licensing, government rights for compulsory licensing,well good for law students
Compulsory licensing Cyril JoseCompulsory Licensing: Regulatory perspective on how it can be filed and how they can be used for public health, especially essential anti-cancer molecules. A tool to scale down the cost of essential life saving medicines
Roche vs cipla patent case studyAniket VaidyaRoche sued Cipla for patent infringement over Cipla's generic version of Roche's cancer drug erlotinib. The single judge ruled in favor of Cipla, noting that Cipla's cheaper generic provided important public access to this life-saving drug. However, the division bench overturned this, finding that Roche's patent was for a mixture of polymorphs while Cipla's drug contained only polymorph B, which was not patented. The court criticized Roche for not properly describing the invention and not providing data to show Cipla's drug infringed the patent. Ultimately, Cipla was found not to infringe Roche's erlotinib patent.
Opposition and revocation of patent ipr presentationRahul Kumar MauryaThe document discusses opposition and revocation of patents in India. It describes pre-grant opposition, which allows opposing the grant of a patent within 3 months of publication. Post-grant opposition allows requesting revocation of a granted patent within 1 year of the grant. Revocation can occur beyond post-grant opposition on grounds such as lacking novelty or inventive steps. The document provides examples of opposition cases, such as Positive Women's Network opposing Boehringer Ingelheim's nevirapine syrup patent, and Cipla opposing Roche's osteoporosis drug patent. It describes who can file for revocation and the grounds for revoking a patent.
Patent opposition procedureAltacit GlobalThe document summarizes the key differences between pre-grant opposition and post-grant opposition of patents in India. Pre-grant opposition can be filed before the grant of a patent while a patent is still pending, allowing any person to oppose the grant of the patent. Post-grant opposition must be filed within 12 months of the patent grant, and allows for revocation of an already granted patent by interested parties. The document outlines the grounds, procedures, authorities, and timelines involved in each type of opposition process in India.
Patent infringementPatSnapThis 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.
Pregrant and Postgrant opposition pptAnumulaSurendraThe document discusses patent opposition in India. It defines patent opposition as a process where third parties can oppose the grant of a patent during specified time periods. There are two types of opposition: pre-grant opposition, where opposition can be filed after publication but before grant; and post-grant opposition, where opposition can be filed within one year of the patent being granted. The grounds for opposition include lack of novelty, prior claims, obviousness, insufficient disclosure, and non-compliance with requirements. The key differences between pre-grant and post-grant opposition are also outlined.
What is IP, Patents in Pharma IndustryAnthony Melvin Crasto Ph.DWhat is IP, Patents in Pharma Industry by Dr Anthony Crasto, a complete guide for patenting in drug synthesis, discovery, process, polymorphs, AN INSIGHT INTO PCT, DATES, CLAIMS, DEFINITIONS ETC, all you want to know about criteria, method mode, advantages etc, EMAIL ME amcrasto@gmail.com, call +91 9323115463
Intellectual Property Rights of Pharmaceuticals Hemanga HazarikaThis document discusses intellectual property rights of pharmaceuticals in India. It provides an overview of the various types of intellectual property covered by legislation in India, including copyright, patents, trademarks, designs, and geographical indications. It also summarizes the patent application process and requirements, as well as exceptions. The impact of patents on the pharmaceutical industry in India is also examined, noting both benefits and challenges. Recent patent disputes involving pharmaceutical companies are also summarized.
Infringement of patents and remediesatuljaybhayeThis 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
Patent Term Extension Case Law In JapankhirayamaThe document discusses three patent term extension cases in Japan regarding later drug approvals. The Intellectual Property High Court ruled that the Japan Patent Office (JPO) could not refuse extension applications without proving the patented invention's prohibition of use was not dissolved by marketing approval or that approved acts did not constitute working the invention. The court also redefined key terms, allowing later dosage form approvals to extend patent terms. This impacts pharmaceutical profitability but could delay patent law reforms until the Supreme Court rules on JPO's appeal.
THE PATENT INFRINGEMENT CASE - NEXIUMADAM SThis document outlines a patent infringement case between AstraZeneca and Ranbaxy regarding AstraZeneca's heartburn medication Nexium. It provides background on both parties and how Ranbaxy sought approval for a generic version. It describes how AstraZeneca sued Ranbaxy for patent infringement, triggering a 30 month stay of FDA approval for Ranbaxy. It then summarizes how AstraZeneca later settled litigation with Ranbaxy and other generic manufacturers, agreeing to drop lawsuits in exchange for the generics admitting patent validity and delaying market entry until May 2014.
Drug PatencyIman AjamiThe document discusses various aspects of drug patents including definitions, requirements, strategies, advantages and disadvantages. It defines a patent as a property right granted to an inventor that allows them to exclude others from making or selling their invention for a limited time in exchange for publicly disclosing the invention. Key requirements for a patent include novelty, inventive step, industrial applicability and sufficiency of disclosure. The document also discusses the role of patents in incentivizing drug development and issues around access to medicines, including evergreening and TRIPS waivers.
PatentAPCER Life SciencesThis document provides information about patents and the Indian patent system. It defines what a patent is, outlines the key features of Indian patent law, and describes the types of patents and application process. The document also includes a sample patent application for a drug delivery technology that uses humic and fulvic acids to improve drug solubility and bioavailability. Key details in the sample include the title, description of invention, drawings, claims, and conclusions section.
natco vs bayer case-finalHelal Uddin MullahThis document provides an overview of the case of Natco Pharma Ltd. vs Bayer regarding the compulsory licensing of the cancer drug Nexavar in India. It discusses how Natco applied for and was granted a compulsory license to produce a generic version at a lower price after Bayer refused to provide a voluntary license or lower the price. The considerations for granting the license included that Bayer had not made the drug sufficiently available or affordable to meet patient needs in India. The verdict upheld the license with some conditions for Natco and increased the royalty rate. The effects may include more compulsory licenses and lower drug prices but potential impacts on innovation.
Revocation , restoration of patent and compulsory licensesViraj Shinde1. This document summarizes key aspects of patent law in India, including who can revoke a patent, grounds for revocation, compulsory licensing, and restoration of lapsed patents.
2. It discusses the first case of compulsory licensing in India, where Natco Pharma received a license for the cancer drug Nexavar, significantly lowering its price in India.
3. The document also outlines the required patent application forms under Indian law.
Compulsory licensing - Talk by Gaurav Mishra at event organized by Departmen...BananaIP CounselsThis presentation is part of the talk delivered by Gaurav Mishra to the participants of a session organized by the department of Science and Technology, Rajasthan. The presentation deals with compulsory licensing of patents in India and gives ab overview of the relevant sections, rules, procedures and case studies.
Compulsory licensing by surendraAnumulaSurendraThis document discusses compulsory licensing of patents in India. Compulsory licensing allows the government to grant a license to a third party to produce a patented product or use a patented process without the consent of the patent holder. The objectives are to reward patent holders while also making patented pharmaceutical products available to the public at affordable prices. Section 84 of the Indian Patent Act lays out the conditions for granting compulsory licenses, such as if the patented invention is not available to the public at a reasonable price. The first compulsory license granted in India was for the cancer drug Nexavar, allowing generic manufacturer Natco to sell a version at a much lower price than the branded version from Bayer.
Patent Overview in Novartis Case pptBizand LegisHuman rights and Patent Overview in Novartis Case power point presentation prepared by Anu B, Legal Intern published by Biz and Legis law firm.
Pharmaceutical patents in india – compulsory licensing, health emergency & af...Rahul DevPharmaceutical patents in india – compulsory licensing, health emergency & affordable healthcare – patent laws in india
pharmaceutical patenting in india, product patent in pharma, india pharmaceutical patent law, pharmaceutical patent cliff, pharmaceutical patent litigation, pharmaceutical patent lawyer, pharmaceutical patent expiry, pharmaceutical patent length, pharmaceutical patent expirations
Case analysis novartis vs union of indiaMohit BajajNovartis challenged the rejection of its patent application for the cancer drug Gleevec in India. The Madras Patent Office rejected the application on the grounds that Gleevec was merely a new salt form of the existing drug imatinib, and did not demonstrate enhanced efficacy as required by Section 3(d) of India's Patents Act. Novartis filed a legal challenge arguing that Section 3(d) violated international trade agreements and India's constitution. The court upheld Section 3(d) as compliant with trade rules and not arbitrary, finding that salt forms with modest improvements did not meet the standard of invention required for patents. The court also found it had jurisdiction to review compliance of domestic laws with international treaties.
Pharmaceutical patent Dr. Amit Gangwal Jain (MPharm., PhD.)Dr. amit gangwal ka pharmaceutical patent presentation
highly exhaustive and updated ppt on pharmaceutical patents, a must watch by all those concerned with the same.
Compulsory licensing (patents)Kumar Saurav Prasadcompulsory licensing of patents in India how to get compulsory licensing in India, procedure, rights involved, act and sections,limitation of compulsory licensing, government rights for compulsory licensing,well good for law students
Compulsory licensing Cyril JoseCompulsory Licensing: Regulatory perspective on how it can be filed and how they can be used for public health, especially essential anti-cancer molecules. A tool to scale down the cost of essential life saving medicines
Roche vs cipla patent case studyAniket VaidyaRoche sued Cipla for patent infringement over Cipla's generic version of Roche's cancer drug erlotinib. The single judge ruled in favor of Cipla, noting that Cipla's cheaper generic provided important public access to this life-saving drug. However, the division bench overturned this, finding that Roche's patent was for a mixture of polymorphs while Cipla's drug contained only polymorph B, which was not patented. The court criticized Roche for not properly describing the invention and not providing data to show Cipla's drug infringed the patent. Ultimately, Cipla was found not to infringe Roche's erlotinib patent.
Opposition and revocation of patent ipr presentationRahul Kumar MauryaThe document discusses opposition and revocation of patents in India. It describes pre-grant opposition, which allows opposing the grant of a patent within 3 months of publication. Post-grant opposition allows requesting revocation of a granted patent within 1 year of the grant. Revocation can occur beyond post-grant opposition on grounds such as lacking novelty or inventive steps. The document provides examples of opposition cases, such as Positive Women's Network opposing Boehringer Ingelheim's nevirapine syrup patent, and Cipla opposing Roche's osteoporosis drug patent. It describes who can file for revocation and the grounds for revoking a patent.
Patent opposition procedureAltacit GlobalThe document summarizes the key differences between pre-grant opposition and post-grant opposition of patents in India. Pre-grant opposition can be filed before the grant of a patent while a patent is still pending, allowing any person to oppose the grant of the patent. Post-grant opposition must be filed within 12 months of the patent grant, and allows for revocation of an already granted patent by interested parties. The document outlines the grounds, procedures, authorities, and timelines involved in each type of opposition process in India.
Patent infringementPatSnapThis 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.
Pregrant and Postgrant opposition pptAnumulaSurendraThe document discusses patent opposition in India. It defines patent opposition as a process where third parties can oppose the grant of a patent during specified time periods. There are two types of opposition: pre-grant opposition, where opposition can be filed after publication but before grant; and post-grant opposition, where opposition can be filed within one year of the patent being granted. The grounds for opposition include lack of novelty, prior claims, obviousness, insufficient disclosure, and non-compliance with requirements. The key differences between pre-grant and post-grant opposition are also outlined.
What is IP, Patents in Pharma IndustryAnthony Melvin Crasto Ph.DWhat is IP, Patents in Pharma Industry by Dr Anthony Crasto, a complete guide for patenting in drug synthesis, discovery, process, polymorphs, AN INSIGHT INTO PCT, DATES, CLAIMS, DEFINITIONS ETC, all you want to know about criteria, method mode, advantages etc, EMAIL ME amcrasto@gmail.com, call +91 9323115463
Intellectual Property Rights of Pharmaceuticals Hemanga HazarikaThis document discusses intellectual property rights of pharmaceuticals in India. It provides an overview of the various types of intellectual property covered by legislation in India, including copyright, patents, trademarks, designs, and geographical indications. It also summarizes the patent application process and requirements, as well as exceptions. The impact of patents on the pharmaceutical industry in India is also examined, noting both benefits and challenges. Recent patent disputes involving pharmaceutical companies are also summarized.
Infringement of patents and remediesatuljaybhayeThis 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
Patent Term Extension Case Law In JapankhirayamaThe document discusses three patent term extension cases in Japan regarding later drug approvals. The Intellectual Property High Court ruled that the Japan Patent Office (JPO) could not refuse extension applications without proving the patented invention's prohibition of use was not dissolved by marketing approval or that approved acts did not constitute working the invention. The court also redefined key terms, allowing later dosage form approvals to extend patent terms. This impacts pharmaceutical profitability but could delay patent law reforms until the Supreme Court rules on JPO's appeal.
THE PATENT INFRINGEMENT CASE - NEXIUMADAM SThis document outlines a patent infringement case between AstraZeneca and Ranbaxy regarding AstraZeneca's heartburn medication Nexium. It provides background on both parties and how Ranbaxy sought approval for a generic version. It describes how AstraZeneca sued Ranbaxy for patent infringement, triggering a 30 month stay of FDA approval for Ranbaxy. It then summarizes how AstraZeneca later settled litigation with Ranbaxy and other generic manufacturers, agreeing to drop lawsuits in exchange for the generics admitting patent validity and delaying market entry until May 2014.
Drug PatencyIman AjamiThe document discusses various aspects of drug patents including definitions, requirements, strategies, advantages and disadvantages. It defines a patent as a property right granted to an inventor that allows them to exclude others from making or selling their invention for a limited time in exchange for publicly disclosing the invention. Key requirements for a patent include novelty, inventive step, industrial applicability and sufficiency of disclosure. The document also discusses the role of patents in incentivizing drug development and issues around access to medicines, including evergreening and TRIPS waivers.
PatentAPCER Life SciencesThis document provides information about patents and the Indian patent system. It defines what a patent is, outlines the key features of Indian patent law, and describes the types of patents and application process. The document also includes a sample patent application for a drug delivery technology that uses humic and fulvic acids to improve drug solubility and bioavailability. Key details in the sample include the title, description of invention, drawings, claims, and conclusions section.
natco vs bayer case-finalHelal Uddin MullahThis document provides an overview of the case of Natco Pharma Ltd. vs Bayer regarding the compulsory licensing of the cancer drug Nexavar in India. It discusses how Natco applied for and was granted a compulsory license to produce a generic version at a lower price after Bayer refused to provide a voluntary license or lower the price. The considerations for granting the license included that Bayer had not made the drug sufficiently available or affordable to meet patient needs in India. The verdict upheld the license with some conditions for Natco and increased the royalty rate. The effects may include more compulsory licenses and lower drug prices but potential impacts on innovation.
Revocation , restoration of patent and compulsory licensesViraj Shinde1. This document summarizes key aspects of patent law in India, including who can revoke a patent, grounds for revocation, compulsory licensing, and restoration of lapsed patents.
2. It discusses the first case of compulsory licensing in India, where Natco Pharma received a license for the cancer drug Nexavar, significantly lowering its price in India.
3. The document also outlines the required patent application forms under Indian law.
Compulsory licensing - Talk by Gaurav Mishra at event organized by Departmen...BananaIP CounselsThis presentation is part of the talk delivered by Gaurav Mishra to the participants of a session organized by the department of Science and Technology, Rajasthan. The presentation deals with compulsory licensing of patents in India and gives ab overview of the relevant sections, rules, procedures and case studies.
Will Nexavar® (Sorafenib Tosylate) Become Unprecedented Case Study? Dr. Amit Gangwal Jain (MPharm., PhD.)The document discusses India granting its first compulsory license to Natco Pharma for the generic version of Nexavar, manufactured by Bayer. It summarizes the key points as follows:
1) Natco Pharma received a compulsory license from India's patent office to produce a generic version of Nexavar at a 97% lower price after Bayer refused to provide a voluntary license.
2) Nexavar is used to treat liver and kidney cancer. Bayer holds the Indian patent but was not making it widely available at an affordable price in India.
3) The ruling sets an important precedent and has wider implications for global pharmaceutical companies' businesses in India, though it also aims to balance intellectual property rights
Rohit sir pptSaurabh waniThis document discusses intellectual property rights (IPR) such as patents, copyrights, and trademarks. It focuses on patents, explaining what they are, how they are granted, requirements for patents, types of patent infringement, limitations of patents, and some notable patent cases from India involving drugs like Turmeric, Neem, and Glivec. Patents provide inventors exclusive rights to commercially use their inventions for a limited time period, usually 20 years, to protect their intellectual property from being copied. The document delves into the patent process and requirements including novelty, non-obviousness, and disclosure of the invention.
Intellectual property rights & Patent filing ProceduresDr.nagabhushanam maddiDetailed information on different types of intellectual property rights and how to protect them through patent filing, copy rights, geographical identification and other procedures
IntellectualpropertyrightssalsadmachingalThe document discusses intellectual property rights in India, including patents, copyrights, trademarks, and the history of related laws. It provides statistics on the size and growth of the Indian pharmaceutical industry. The top selling drug brands in India are also mentioned, such as Crocin, Corex, and Phensedyl cough syrup. The process for obtaining a patent and the duration of different types of intellectual property rights are summarized as well.
TTC newsletter Volume 4TT ConsultantsThis document provides news headlines about intellectual property from India, China, and Japan. The headlines cover a range of IP-related topics, including patents granted, compulsory licensing, copyright issues, and trademark rulings. The document also includes an editorial section from TT Consultants on IP topics.
Biosimilars: A U.S. PerspectivePatterson Thuente IPThis document discusses biosimilars regulation in the United States. It provides background on biosimilars and the Biologics Price Competition and Innovation Act (BPCIA) that established an approval pathway for biosimilars. The BPCIA requires biosimilars to be "highly similar" to an FDA-approved biologic and created provisions for resolving patent disputes between innovators and biosimilar applicants known as the "patent dance." A key case, Amgen v. Sandoz, addressed whether biosimilar applicants must follow the patent dance and provide notice of commercial marketing after FDA approval. The U.S. Solicitor General recommended the Supreme Court review issues in the case that will impact
Indian Intellectual Property Cases Report, 2021.pdfBananaIP CounselsBananaIP is happy to launch the IP Cases Report for the year 2021. This report covers cases related to intellectual property decided by Courts in India, in the form of case notes. These case notes cover important decisions on critical questions of law and fact with respect to various species of intellectual property.
Generic drugs product developmentSachin GThis document provides a summary of a presentation on generic drugs. It discusses the definition of generic drugs, the generic drug development and approval process, provisions of the Hatch-Waxman Act, and relevant sections of the Code of Federal Regulations. The summary highlights that a generic drug must be equivalent to the branded version in ingredients, dosage, safety and efficacy. It also outlines the steps in generic drug approval via an Abbreviated New Drug Application, including requirements for bioequivalence testing and patent certifications. Additionally, it notes provisions established by the Hatch-Waxman Act related to patent term extensions and patent challenges involved in the generic approval pathway.
Patents (With Popular Indian Case Studies)JASTINDER PAL SINGHPatents, copy-write, trademark, procedure of patents, Intellectual Property, Compulsory Licensing
Basmati Rice Patent Case (Rice Tec V/s India)
Bayer V/s NATCO Licensing Case
Freedom to OperateAshwani DhingraFreedom to Operate (FTO) refers to whether it’s commercially ‘safe’ for you to make or sell your product in the country in which you wish to do so, without infringing existing third-party rights.
Indian patent act - 1970VanithaVaniN1Indian patent act - 1970 - definitions, history, types, terms, inventions patentable and non-patentable, patent filling procedure, rights of a patentee, offences and penalties.
Intellectual property litigations: A case study of Anticancer drug Glivec in ...Dr Shahid SaacheThis presentation include brief about various intellectual property rights in India like patent, copyright, trademarks etc. It also include a detailed case discussion of Novartis anticancer drug Glivec i.e imatinib mesylate which is a patent case.
Origins of India's Patent LawAmanda BoddingtonIndia is no newcomer to patent protection. The discussion on having a law to protect inventions goes back as far as 1832. After a number of failed attempts, the first Patents Act of India, essentially a copy of British patent law, was finally enacted in 1856. A series of adaptations followed, again modeled on changes in British law.
PATENT.pptxARTINADEKAThe document discusses patents and intellectual property. It defines intellectual property as creations of the mind such as inventions, literary works, designs, and symbols. It notes that inventors need rights to protect their intellectual property and make a fair return on their investments. The document then summarizes the different categories of intellectual property including patents, trademarks, copyrights, and others. It provides details on what can be patented, the patent application process, and commercializing a patent through licensing.
Novartis V. Union of India (2013) 6 SCC 1.pptxNancyGarg60The Supreme Court upheld the rejection of Novartis' patent application for the drug Glivec. The court found that the beta-crystalline form of imatinib mesylate did not result in enhanced therapeutic efficacy over existing forms of the drug as required by Section 3(d) of the Indian Patent Act. The court also held that Section 3(d) was not unconstitutional as it aims to prevent "evergreening" of patents and promotes access to affordable life-saving drugs for Indian citizens. Novartis' appeal argued the provisions were vague and violated intellectual property rights, but the court disagreed and affirmed the patent rejection.
Para i iv orange bookAltacit GlobalThe document discusses the Hatch-Waxman Act and its role in facilitating generic drug approvals in the US. It introduced the Abbreviated New Drug Application (ANDA) process which allows generics to piggyback on the clinical trial data of branded drugs. The Act also established the Orange Book database which lists drug patents. Generic companies can file ANDAs with certifications (Paras I-IV) regarding the patents. Para IV filings are the most complex and involve claims of non-infringement or patent invalidity, often leading to litigation between generic and branded companies. The Act aimed to balance increased generic competition with incentives for continued drug innovation.
Rabies Bali 2008-2020_WRD Webinar_WSAVA 2020_Final.pptxWahid HuseinA decade of rabies control programmes in Bali with support from FAO ECTAD Indonesia with Mass Dog Vaccination, Integrated Bite Case Management, Dog Population Management, and Risk Communication as the backbone of the programmes
Enzyme Induction and Inhibition: Mechanisms, Examples & Clinical SignificanceSumeetSharma591398This presentation explains the crucial role of enzyme induction and inhibition in drug metabolism. It covers:
✔️ Mechanisms of enzyme regulation in the liver
✔️ Examples of enzyme inducers (Rifampin, Carbamazepine) and inhibitors (Ketoconazole, Grapefruit juice)
✔️ Clinical significance of drug interactions affecting efficacy and toxicity
✔️ Factors like genetics, age, diet, and disease influencing enzyme activity
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India’s first compulsory license upheld, but legal
1. India’s First Compulsory License
CL issued to Natco Pharma
BY……….
Harishankar Sahu
Hemant Chandwani
Dhruv Malha
2. Headlines
• New Delhi – India’s Intellectual Property Appellate Board (IPAB) upheld the
country’s first compulsory licence on a pharmaceutical product.
• The much-awaited verdict by Justice (Ms) Prabha Sridevan upholds the
compulsory licence issued to Hyderabad-based Natco Pharma Ltd, an Indian
generic drug manufacturer, which sells a much cheaper version of German
pharmaceutical company Bayer AG’s kidney and liver cancer drug Nexavar in
the market.
• Bayer on 5 March announced it will appeal the decision (IPW, Developing
Country Policy, 5 March 2013).
Vs.
3. Background
• Bayer holds an Indian patent for the chemotherapy drug sorafenib
tosylate, sold under the trade name Nexavar. On 9 March 2012, the then
Indian Patent Controller issued the first-ever compulsory licence to Natco
Pharma to manufacture an affordable generic version of sorafenib
tosylate.
• Bayer promptly filed an appeal against the compulsory licence order
before the IPAB in Chennai. Meanwhile, the CL had a dramatic effect on
the drug’s price – bringing it down to 8,800 rupees (approximately USD
160) for a month’s dose – a fraction of Bayer’s price of 280,000 rupees
(approximately 5,098 USD). Under the terms of the compulsory licence,
however, Bayer got a six per cent royalty on sales by Natco.
4. • The IPAB decision comes at a time when the final verdict on another
landmark case involving patents and pharma is awaited in India. Novartis
is seeking patent protection for the most recent formulation of its
blockbuster leukemia drug, imatinib, sold as as Gleevec in the United
States and Glivec in India.
Background (Con.)
5. • The mechanism of compulsory license, which has generated a lot of heat
globally, is embedded in India’s patent law. Section 84 of India’s Patents Act
provides that an interested person may apply for a compulsory license to
work the patented invention on any of the grounds.
• Granting the CL to Natco reinvigorated the old battle between multinational
pharmaceutical companies and the country’s generic drug manufacturers.
• Sridevan cited affordability and product access as the reasons for the
decision to dismiss Bayer’s appeal against the compulsory licence (CL).
However, the Chennai-based IPAB hiked the royalty which Natco would have
to pay to Bayer (under the terms of the CL) from 6 per cent to 7 per cent.
• Mr. Madineedi Adinarayana, company secretary and general manager
of Legal and Corporate Affairs at Natco Pharma Ltd, told Intellectual
Property Watch that the IPAB decision is “very significant” and he is
“happy” that the CL had been upheld. But, he said, “This is unlikely to be
the end of the legal battle.”
Case
6. • Bayer spokesperson had said, “We strongly disagree with the conclusions
of the Patent Controller of India and have appealed his order on May 4th
2012 with the Intellectual Property Appellate Board. We will rigorously
continue to defend our intellectual property rights which are a
prerequisite for bringing innovative medicines to patients” (IPW, Public Health,
20 May 2012).
Case
7. Conclusion
• Through the whole case we relieve with the decision by the
IPAB to uphold India’s first compulsory license. The decision
confirms that the Indian Patent Office is able to use all the
means legally at its disposal to check the abuse of patents and
open up access to affordable versions of patented medicines.”