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1.
PLoS One ; 19(5): e0303802, 2024.
Article in English | MEDLINE | ID: mdl-38768189

ABSTRACT

The innovative performance of manufacturing and service companies can be impacted by the existing relationship between open innovation (OI) and the generation of confidentiality agreements (NDAs) as a tool for the protection of intellectual property. Based on the analysis of a cross-sectional sample of 6,798 industrial companies (2019-2020) and 9,304 companies in the service sector (2017-2019) that are part of the directory of the National Administrative Department of Statistics (DANE) in its Technological Innovation and Development Survey (EDIT and EDITS), it can be suggested that the interaction of these two variables (OI and NDAs) generate positive effects for the manufacturing industry but negative ones for the service sector. It could be deduced that the positive effect is due to the greater tradition of OI in the manufacturing industry and the negative effect to the caution that the service sector presents when collaborating with external actors.


Subject(s)
Confidentiality , Humans , Cross-Sectional Studies , Manufacturing Industry , Inventions , Intellectual Property , Industry , Surveys and Questionnaires
2.
J Drugs Dermatol ; 23(5): 347-352, 2024 May 01.
Article in English | MEDLINE | ID: mdl-38709700

ABSTRACT

This paper outlines a process undertaken by a physician to design a peptide aimed at impacting the extracellular matrix. From a position of very little expertise, a new peptide was designed with amino acid constituents based on the structural proteins collagen and elastin. Sequencing was also considered, given the periodic repetition observed in these proteins, and a peptide with reasonable molecular weight and physical characteristics was designed using available software. The sequence of events concerning intellectual property, functionality investigation, and eventual use of the peptide in new formulations is detailed. This may be of interest to physicians who consider this exercise out of the scope of the usual practice. J Drugs Dermatol. 2024;23(5):347-352.    doi:10.36849/JDD.7921.


Subject(s)
Peptides , Humans , Peptides/chemistry , Drug Design , Elastin/chemistry , Collagen/chemistry , Extracellular Matrix , Intellectual Property , Physicians
3.
PLoS Med ; 21(4): e1004381, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38662775

ABSTRACT

In this Policy Forum piece, Robin Feldman discusses how current legislation contributes to informational deficits around drug patents for biologic drugs in the United States.


Subject(s)
Biosimilar Pharmaceuticals , Intellectual Property , United States , Humans , Biological Products , Patents as Topic/legislation & jurisprudence , Legislation, Drug , United States Food and Drug Administration/legislation & jurisprudence
4.
Glob Public Health ; 19(1): 2335360, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38626321

ABSTRACT

Despite self-congratulatory rhetoric, Canada compromised COVID-19 vaccine equity with policies impeding a proposed global waiver of vaccine intellectual property (IP) rules. To learn from Canada's vaccine nationalism we explore the worldview - a coherent textual picture of the world - in a sample of Government of Canada communications regarding global COVID-19 vaccine sharing. Analysed documents portray risks and disparities as unrelated to the dynamics and power relations of the Canadian and international economies. Against this depoliticised backdrop, economic growth fueled by strict IP rules and free trade is advanced as the solution to inequities. Global vaccine access and distribution are pursued via a charity-focused public-private-partnership approach, with proposals to relax international IP rules dismissed as unhelpful. Rather than a puzzling lapse by a good faith 'middle power', Canada's obstruction of global COVID-19 vaccine equity is a logical and deliberate extension of dominant neoliberal economic policy models. Health sector challenges to such models must prioritise equity in global pandemic governance via politically assertive and less conciliatory stances towards national governments and multilateral organisations. Mobilisation for health equity should transform the overall health-damaging macroeconomic model, complementing efforts based on specific individual health determinants or medical technologies.


Subject(s)
COVID-19 Vaccines , COVID-19 , Humans , Pandemics/prevention & control , COVID-19/epidemiology , COVID-19/prevention & control , Canada/epidemiology , Intellectual Property , Global Health
5.
PLoS One ; 19(4): e0302693, 2024.
Article in English | MEDLINE | ID: mdl-38662668

ABSTRACT

Intellectual property is crucial for the development of firms. At the micro level, firm comprehensive intellectual property ability involves abilities about intellectual property creation, utilization, protection, and management. In order to develop the comprehensive intellectual property ability of firms, the China National Intellectual Property Administration began to implement the national intellectual property demonstration advantage firm (NIPDAF) policy in 2013. Based on this exogenous policy shock, using data from listed companies from 2011 to 2020 as the research sample, the time-varying DID method is used to test the impact of the NIPDAF policy intended to cultivate comprehensive intellectual property ability on firm productivity. The results show that after policy implementation, the total factor productivity of NIPDAFs increased by about 3.3% compared to the control group. This finding is robust after a series of tests. Furthermore, the NIPDAF policy promotes firm productivity through stimulating technology innovation, improving investment efficiency, and enhancing competitive advantage. In addition, the NIPDAF policy has a more significant incentive effect on the total factor productivity of non-state-owned enterprises, firms in the eastern region, and firms in patent intensive industries.


Subject(s)
Intellectual Property , China , Efficiency , Humans , Policy , Industry , Investments
6.
Neural Netw ; 174: 106199, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38452664

ABSTRACT

With the widespread application of deep neural networks (DNNs), the risk of privacy breaches against DNN models is constantly on the rise, resulting in an increasing need for intellectual property (IP) protection for such models. Although neural network watermarking techniques are widely used to safeguard the IP of DNNs, they can only achieve passive protection and cannot actively prevent unauthorized users from illicit use or embezzlement of the trained DNN models. Therefore, the development of proactive protection techniques to prevent IP infringement is imperative. To this end, we propose SecureNet, a key-based access license framework for DNN models. The proposed approach involves injecting license keys into the model through backdoor learning, enabling correct model functionality only when the appropriate license key is included in the input. To ensure the reusability of DNN models, we also propose a license key replacement algorithm. In addition, based on SecureNet, we designed defense mechanisms against adversarial attacks and backdoor attacks, respectively. Furthermore, we introduce a fine-grained authorization method that enables flexible granting of model permissions to different users. We have designed four license-key schemes with different privileges, tailored to various scenarios. We evaluated SecureNet on five benchmark datasets including MNIST, Cifar10, Cifar100, FaceScrub, and CelebA, and assessed its performance on six classic DNN models: LeNet-5, VGG16, ResNet18, ResNet101, NFNet-F5, and MobileNetV3. The results demonstrate that our approach outperforms the state-of-the-art model parameter encryption methods by at least 95% in terms of computational efficiency. Additionally, it provides effective defense against adversarial attacks and backdoor attacks without compromising the model's overall performance.


Subject(s)
Learning , Neural Networks, Computer , Algorithms , Benchmarking , Intellectual Property
7.
Recent Pat Biotechnol ; 18(2): 128-143, 2024.
Article in English | MEDLINE | ID: mdl-38282443

ABSTRACT

The current Intellectual Property Rights (IPR) framework supports the commercialization of seed improvement, monoculture, and the patent protection of novel plant varieties, microorganisms, and genetically modified animals. As a consequence, our rich biogenetic diversity is irreversibly dissipating. However, we need to figure out how to create a methodology for elective choices that will achieve harmony between the official Intellectual Property (IP) structure and maintainable biodiversity components. The majority of the biotechnology sector's programmes in India are managed by the Department of Biotechnology. It is under the Ministry of Science and Technology. Its goals are to provide services in the fields of study, infrastructure, human resource development, biotechnology popularisation, industry promotion, and establishment of centres of excellence. Implementation of practise biosafety regulations for genetically modified organisms, recombinant DNA products, and programmes is based on biotechnology for the good of society. This creates an information network for India's bioinformatics mission in the local, national, and worldwide scientific community.


Subject(s)
Inventions , Patents as Topic , Animals , Humans , Biotechnology/methods , Intellectual Property , India
8.
J Autism Dev Disord ; 54(4): 1594-1604, 2024 Apr.
Article in English | MEDLINE | ID: mdl-36637589

ABSTRACT

Intellectual disability in India is substantially under-reported, especially amongst females. This study quantifies the prevalence and gender bias in household reporting of intellectual disability by estimating the age-and-gender specific prevalence of the intellectually disabled by education, Socio-Demographic Index (SDI) score, place of residence, (rural/urban) and income of household head. We estimated prevalence (per 100,000) at 179 (95% CI: 173 to 185) for males and 120 (95% CI: 115 to 125) for females. Gender differences declined sharply with increased education, was higher for lower ages and low income and varied little by state development. Under-identification and under-reporting due to stigma are two plausible reasons for the gender differences in prevalence that increase with age.


Subject(s)
Autism Spectrum Disorder , Disabled Persons , Intellectual Disability , Humans , Male , Female , Prevalence , Intellectual Disability/epidemiology , Socioeconomic Factors , Sexism , India/epidemiology
9.
J Health Polit Policy Law ; 49(1): 9-42, 2024 Feb 01.
Article in English | MEDLINE | ID: mdl-37522338

ABSTRACT

CONTEXT: To facilitate the manufacturing of COVID-19 medical products, in October 2020 India and South Africa proposed a waiver of certain intellectual property (IP) provisions of a World Trade Organization (WTO) agreement. After nearly two years, a narrow waiver agreement that did little for vaccine access passed the ministerial despite the pandemic's impact on global trade, which the WTO is mandated to safeguard. METHODS: The authors conducted a content analysis of WTO legal texts, key-actor statements, media reporting, and the WTO's procedural framework to explore legal, institutional, and ideational explanations for the delay. FINDINGS: IP waivers are neither legally complex nor unprecedented within WTO law, yet these waiver negotiations exceeded their mandated 90-day negotiation period by approximately 18 months. Waiver opponents and supporters engaged in escalating strategic framing that justified and eventually secured political attention at head-of-state level, sidelining other pandemic solutions. The frames deployed discouraged consensus on a meaningful waiver, which ultimately favored the status quo that opponents preferred. WTO institutional design encouraged drawn-out negotiation while limiting legitimate players in the debate to trade ministers, empowering narrow interest group politics. CONCLUSIONS: Despite global political attention, the WTO process contributed little to emergency vaccine production, suggesting a pressing need for reforms aimed at more efficient and equitable multilateral processes.


Subject(s)
COVID-19 , Vaccines , Humans , International Cooperation , Negotiating , COVID-19/epidemiology , Commerce , Politics , Intellectual Property
10.
Recent Pat Biotechnol ; 18(3): 241-256, 2024.
Article in English | MEDLINE | ID: mdl-37605394

ABSTRACT

BACKGROUND: Morus nigra L. is a plant with significant potential for drug development due to the presence of numerous bioactive compounds in its various parts. OBJECTIVES: This article aims to compile the technological perspectives of Morus nigra L. towards drug development and therapeutic indications based on registered patents in databases. METHODS: The study analyzed patents published within the last five years, focusing on products derived from different parts of the Morus nigra L. plant. Patent databases such as the European Patent Office (EPO), the United States Patent and Trademark Office (USPTO), the World Intellectual Property Organization (WIPO), and the National Institute of Industrial Property Databases (INPI) were examined. RESULTS: A total of 45 patents were categorized by country of origin, type of applicant, extraction method, and therapeutic indications. China had the highest number of patent filings (43.48%), and private companies were the primary technology patent holders (38.64%). Noteworthy extraction methods included ultrasound-assisted extraction, decoction, infusion, and maceration. The most utilized plant parts were leaves (44.44%), followed by fruits (35.56%), root bark (15.56%), and stems (4.44%). The main therapeutic indications identified were the treatment of hyperglycemia and dyslipidemia (43.33%), along with digestive problems, cosmetics, nutrition, and cleaning applications. CONCLUSION: The study of patents covers discoveries and advancements often absent in scientific articles, making a review focused on this advanced information crucial for expanding existing scientific knowledge. Even if some therapies have been explored previously, patents can reveal innovative approaches and fresh perspectives that contribute to sustained scientific progress.


Subject(s)
Morus , Databases, Factual , Intellectual Property , Patents as Topic , Technology , United States
11.
Mol Inform ; 43(1): e202300221, 2024 Jan.
Article in English | MEDLINE | ID: mdl-38010631

ABSTRACT

The availability of patent chemical data offers public access to a chemical space that is not well covered by other sources collecting small molecules from scholarly literature. However, open applications to facilitate the search and analysis of biologically-relevant molecular structures present in patents are still largely missing. We have developed CIPSI, an open Chemical Intellectual Property Service @ IMIM to assist medicinal chemists in searching and analysing molecules in SureChEMBL patents. The current version contains 6,240,500 molecules from 236,689 pharmacological patents, of which 5,949,214 are confidently assigned to core chemical structures reminiscent of the Markush structure in the patent claim. The platform includes some graphical tools to facilitate comparative patent analyses between drugs, chemical substructures, and company assignees. CIPSI is available at https://cipsi.org.


Subject(s)
Intellectual Property , Molecular Structure
12.
Trends Biotechnol ; 42(3): 258-260, 2024 03.
Article in English | MEDLINE | ID: mdl-37980185

ABSTRACT

As China emerges as a synthetic biology (synbio) global leader, it faces distinct science-society challenges. Our series offers a snapshot of China's synbio state, emphasizing the intersection and its policy implications. The debut piece elucidates the intellectual property rights (IPR)-funding interplay in China's expanding synbio territory, underlining its key role in driving innovation and commercialization.


Subject(s)
Intellectual Property , Synthetic Biology , China , Policy
14.
Rev. derecho genoma hum ; (59): 55-88, jul.-dic. 2023.
Article in Spanish | IBECS | ID: ibc-232449

ABSTRACT

La expiración de patentes farmacéuticas sobre medicamentos favorece la realización de prácticas comerciales dentro del sector que obstaculizan la entrada de los medicamentos genéricos. La creación de terapias digitales a través de la incorporación de componentes digitales en productos farmacéuticos tradicionales es una alternativa innovadora que combina la aportación de un valor añadido a un producto farmacéutico obsoleto a la vez que aborda problemas sanitarios serios de forma transformadora. Este tipo de prácticas podría ayudar a las empresas farmacéuticas a mantener su hueco de mercado tras la expiración de la patente de un medicamento superventas. (AU)


The expiry of pharmaceutical patents on medical products encourages commercial practices within the sector that hinder the entry of generic medicines. The creation of digital therapies through the incorporation of digital components into traditional pharmaceuticals is an innovative alternative that combines adding value to an obsolete pharmaceutical product while addressing serious health problems in a transformative way. Such practices could help pharmaceutical companies to maintain their market niche after the patent expiry of a blockbuster drug. (AU)


Subject(s)
Intellectual Property of Pharmaceutic Products and Process , Drug Stability , Legislation, Drug , Inventions
15.
BMJ Glob Health ; 8(11)2023 11 30.
Article in English | MEDLINE | ID: mdl-38035734

ABSTRACT

This article aims to propose practical solutions that coordinate the conflicting interests between the global community and the pharmaceutical industry on the intellectual property (IP) waiver for COVID-19 vaccines and facilitate a more equitable vaccine supply chain in the post-COVID-19 world. We critically conducted a narrative literature review to identify procedural and practical issues in the current vaccine supply chain. The search was conducted across various academic disciplines, including biomedical science, life science, law and social science, using resources such as PubMed, Web of Science, Scopus and Westlaw. After screening 731 articles, 55 studies were selected for review. The narrative review revealed several critical barriers that hinder vaccine supply in less-developed countries (LDCs) as follows: (1) WTO Trade-Related Aspects of Intellectual Property Rights (TRIPs) waiver requests may not be granted due to its stringent consensus rule; (2) the current compulsory license system may not work due to the complexity of IP rights covering COVID-19 vaccine technologies; (3) only a few LDCs have domestic companies capable of manufacturing vaccines, and (4) political and economic tensions among countries exacerbate existing barriers to vaccine distribution in LDCs. Based on these findings, we proposed a comprehensive compulsory license system, which combines TRIPS's compulsory license system with the third-party beneficiary mechanism under Common Law. This integrated approach offers a balanced solution that ensures fair compensation for vaccine developers while facilitating broader vaccine access.


Subject(s)
COVID-19 , Vaccines , Humans , COVID-19/prevention & control , COVID-19 Vaccines/supply & distribution , Intellectual Property , International Cooperation
20.
Cad. Ibero Am. Direito Sanit. (Impr.) ; 12(3): 180-192, jul.-set.2023.
Article in Portuguese | LILACS | ID: biblio-1510790

ABSTRACT

Objetivos: identificar em que medida as iniquidades em saúde sempre foram integradas por injustas distribuições de poder, quais seriam as facetas principais dessa assimetria e em que realidades práticas elas mais se manifestam. Metodologia: revisão crítica de documentos produzidos em conferências e projetos internacionais relacionados à governança em saúde, aliada à revisão narrativa de textos científicos que tangenciam as temáticas neoinstitucionalistas. Resultados: desde a percepção inicial sobre os determinantes sociais da saúde, fez-se referência a determinantes políticos (em especial, a injusta distribuição de poder). O projeto Global Governance for Health evidenciou convir que os determinantes políticos sejam tratados em separado, pois, em certa medida, são os determinantes dos determinantes sociais. Os principais déficits políticos que afetam a tomada de decisão na área da saúde e impedem que sejam superadas as iniquidades em saúde são cinco: a) representatividade; b) transparência; c) adaptabilidade; d) intersetorialidade; e) regulação. As situações em que esses déficits se mostram mais evidentes são sete: i) diante da necessidade histórica de medidas de austeridade financeira; ii) no âmbito das políticas protecionistas dos detentores de propriedade industrial e intelectual; iii) na seara dos acordos de investimentos; iv) no âmbito do mercado de alimentos; v) diante da opção de deixar certas atividades corporativas desreguladas, vi) frente a opção de excluir os migrantes das tomadas de decisão; vii) diante da violência armada. Conclusão: o não enfrentamento das disfunções políticas de governança da saúde faz com que sejam mantidas as iniquidades de saúde e até mesmo cria ou agrava novas iniquidades.


Objectives: to identify the extent to which health inequities have always been integrated by unfair distributions of power, what would be the main facets of this asymmetry and in which practical realities they are most manifested. Methods: critical review of documents produced at international conferences and projects related to health governance, combined with a narrative review of scientific texts that touch on neo-institutionalist theme. Results: since the initial perception about the social determinants of health, reference has been made to political determinants (in particular, the unjust distribution of power). The Global Governance for Health project has shown that political determinants should be treated separately, as they are, to some extent, the determinants of social determinants. The main political deficits that affect health decision-making and prevent health inequities from being overcome are five: a) representativeness; b) transparency; c) adaptability; d) intersectorality; e) regulation. The situations in which these deficits are most evident are seven: i) in the face of the historical need for financial austerity measures; ii) in the context of protectionist policies of industrial and intellectual property holders; iii) in the area of investment agreements; iv) in the context of the food market; v) in the face of the option to leave certain corporate activities unregulated; vi) in the face of the option to exclude migrants from decision-making; vii) in the face of armed violence. Conclusion: failure to address the political dysfunctions of health governance means that health inequities are maintained and even creates or exacerbates new inequities.


Objetivos: identificar en qué medida las inequidades en salud siempre han estado integradas por distribuciones injustas de poder, cuáles serían las principales facetas de esa asimetría y en qué realidades prácticas se manifiestan más. Metodología: revisión crítica de documentos producidos en congresos y proyectos internacionales relacionados con la gobernanza sanitaria, combinada con una revisión narrativa de textos científicos que tocan temas neoinstitucionalistas. Resultados: desde la percepción inicial de los determinantes sociales de la salud, se ha hecho referencia a los determinantes políticos (en particular, a la injusta distribución del poder). El proyecto Global Governance for Health ha demostrado que los determinantes políticos deben tratarse por separado, ya que, en cierta medida, son los determinantes de los determinantes sociales. Los principales déficits políticos que afectan a la toma de decisiones sanitarias y impiden superar las desigualdades en salud son cinco: a) representatividad; b) transparencia; c) adaptabilidad; d) intersectorialidad; e) regulación. Las situaciones en las que estos déficits son más evidentes son siete: i) ante la necesidad histórica de medidas de austeridad financiera; ii) en el contexto de las políticas proteccionistas de los titulares de la propiedad industrial e intelectual; iii) en el ámbito de los acuerdos de inversión; iv) en el contexto del mercado alimentario; v) ante la opción de dejar sin regulación determinadas actividades empresariales; vi) ante la opción de excluir a los migrantes de la toma de decisiones; vii) ante la violencia armada. Conclusión: no abordar las disfunciones políticas de la gobernanza sanitaria significa que las desigualdades en salud se mantienen e incluso crean o exacerban nuevas desigualdades.


Subject(s)
Health Law
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