日本アイアール Product Lineup

This seminar explains the fundamentals of bioreactors, covering the basic principles of container, equipment, and operation design, as well as important considerations for application to various types of cells. It focuses on biomanufacturing based on material balance and kinetics, addressing the formulation of reactions within bioreactors, application to operational design, methodologies for scale-up, and considerations in the culture of microorganisms, animal cells, iPS cells, and plant cells. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar aims to acquire basic knowledge necessary for instrumentation design, including the meaning and purpose of instrumentation, an explanation of instruments which are fundamental to instrumentation, and knowledge to interpret instrumentation design documents. The seminar will explain instruments and instrumentation symbols, and exercises will be conducted in each chapter. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course that visually and systematically explains the fundamentals to applications of spectroscopic ellipsometry, as well as measurement and analysis know-how. Participants will learn the essence of dielectric constant and refractive index, the basics and principles of spectroscopic ellipsometry, and through demonstrations of fitting analysis, they will learn how to proceed with analysis and key points for constructing optical models. Case studies on multilayer films, effective medium approximation, surface roughness, and optically anisotropic films will also be covered. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain the amendments to the Labor Safety and Health Act that came into effect in April 2026, focusing particularly on the strengthening of chemical substance management. It will cover the transition from the previous management centered on certain specified chemical substances to a system that manages all chemical substances according to their risks, the expansion of the obligation to provide Safety Data Sheets (SDS), the mandatory measurement of individual exposure, the obligation to appoint chemical substance managers, key points regarding corporate operational systems and responses, and other amendments. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will reset conventional images and misconceptions about GND, deepen understanding of its essential role, and explain EMC design methods using simulations that can be immediately applied from the circuit diagram design stage. It will introduce specific approaches for designing with EMC considerations from the early stages of design, focusing on power and signal lines, as well as concepts and techniques for practical wiring design of printed circuit boards. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar aims to provide an understanding of the fundamental principles and theories related to the dynamics and performance of automobiles, focusing on the basic functions and technologies of vehicles, namely "moving, turning, and stopping." It will cover topics such as maneuverability and stability, ride comfort and vibrations, braking performance, rolling resistance and power performance, new automotive technologies, human-vehicle system dynamics, research and applications of driving simulators, and next-generation automotive technologies. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain the development and entry processes specific to regulated industries that are required for new entrants in the medical and healthcare fields. Taking into account the risks of setbacks due to insufficient understanding of regulations and deficiencies in the application of QMS in the early stages of development, we will systematically explain practical know-how to avoid "pitfalls" during entry, based on our experience of consulting over 500 companies and on-site practices. This includes an overview of business permits, QMS, commercialization, schedule design considering regulatory classifications, exit strategies from the development stage, and the utilization of public support. *For more details, please check the related links or the seminar details in the catalog.

• Technical Seminar

This seminar will systematically explain how to discover and screen early-stage seeds from academia and drug discovery startups from the perspective of pharmaceutical companies, and how to evaluate the feasibility and business potential based on the Target Product Profile (TPP) through Scientific/Translational Drug Development (DD). It will cover the process of filling data gaps with additional tests and validations, nurturing seeds while sharing roles with academia and startups, and making decisions on re-evaluation or postponement after acquiring additional data. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain the creation procedures, key points, considerations, and utilization methods of control plans required by IATF 16949, using specific examples. Leveraging knowledge from the CP Reference Manual and taking into account the contents of the CP Manual issued in 2024, we will introduce the concepts, creation methods, and utilization methods of control plans that are useful for managing manufacturing processes. The program will cover an overview of control plans, the requirements of IATF 16949, creation procedures, interpretation, an overview of the first edition of the CP Manual, and exercises on creation and interpretation. *For details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain how to incorporate generative AI into the workflow, using a fictional patent case as a subject, covering everything from preparing a patent application to creating application documents and handling intermediate processes. It will address the division of roles between generative AI and humans, workflow design, organizing the invention content, prior art searches, drafting claims, specifications, and drawings, responding to rejections, and integrating these practices into business, through lectures and demonstrations. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will clarify who needs what information to make judgments as a starting point for IP landscape analysis and explain how to set appropriate questions. It will introduce methods for incorporating dialogue with relevant departments, organizing discussion points using generative AI, designing searches, forming hypotheses, comparing technologies and companies, conducting scenario analysis, and creating potential winning strategies. Through multiple hypothetical cases, it will demonstrate how to derive winning strategies from analysis results and how to rearrange proposal stories according to the audience. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain the creation procedures, key points, considerations, and utilization methods of FMEA, which are required for the automotive industry's QMS standard IATF 16949 and the European automotive industry's VDA standard, through specific examples. It will cover the concept of FMEA, its history and development, the D/P-FMEA creation procedures based on case studies, evaluation criteria, considerations and key points when applying it, and the integrated FMEA of AIAG & VDA, along with practical exercises. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will cover the 2026 revisions of ISO 9001 and ISO 14001, explaining the key points of the revisions and practical aspects of the transition. We will compare the differences with the 2015 version point by point, discuss alignment with Annex SL, address climate change and sustainability responses, outline the planning for changes, and explain the shifts in the approach to documented information. Additionally, we will provide specific examples to explain how to create a gap analysis sheet, key points for revising manuals, regulations, and forms, internal audit checklists, and how to reflect these in management review minutes. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course designed to cultivate logical thinking skills by training "shape recognition" and "spatial awareness," enabling participants to correctly understand and utilize drawings. It covers the differences between 2D and 3D in design, methods for representing three-dimensional shapes in two-dimensional plans, and expressing ideas using sketches. Participants will engage in exercises such as sketching three-dimensional images, dividing and combining shapes, and assembling three-dimensional models. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is aimed at intellectual property personnel and will provide a practical explanation of the overall picture of pharmaceutical development, including the basics of CMC, quality assurance, PMDA review, how to read CTD, technology transfer, comparability, and the distinction between trade secrets and patents. It will also cover advanced modalities, competitive analysis using public CTDs and PMDA review reports, and the role of the intellectual property department in technology transfer and licensing agreements with CDMOs. *For details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will focus on the fields of "cancer" and "infectious diseases," explaining the essential technological elements, development schemes, processes for solving challenges, and future prospects necessary for the business development of related diagnostic drugs, taking into account the latest regulatory trends. It will cover the latest trends in in vitro diagnostic drugs, biomarkers and companion diagnostics, rapid diagnosis of infectious diseases, factors that differentiate success from failure, and the importance of overall design. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar aims to help participants understand the principles of heat generation and heat transfer in electronic devices, enabling quantitative thermal design through mathematical formulation, and acquiring knowledge for thermal transient analysis using SPICE. It will cover the three elements of heat conduction, thermal calculations, the current-voltage characteristics of MOSFETs, thermal circuit networks and SPICE simulations, self-heating of MOSFETs, and the creation of self-heating MOSFET models and thermal simulations. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is aimed at individuals newly assigned to departments related to pharmaceutical GMP and those responsible for pharmaceutical manufacturing operations. It will explain what regulations (GMP) need to be complied with and what their objectives are. The seminar will cover the basic elements of GMP regulations necessary to grasp the overall picture of GMP, including pharmaceuticals, the Japanese legal system, the origins of GMP, GMP compliance inspections, and the management tasks stipulated by GMP regulations. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar systematically organizes the basic concepts of CSV and standard lifecycle management, explaining the risk-based approach as indicated by GAMP5 2nd Edition and CSA using practical examples. It will cover practical steps for CSV activities using examples of cloud implementation, addressing CSV compliance for data integrity and AI, as well as a live Q&A session. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course on how to write "technical documents that clearly convey content," which cannot be done by AI, emphasizing the importance of creating technical documents with the reader in mind. It will address the difference between "conveying content" and "conveying content 'clearly'," and discuss the mindset needed to establish technical documents as a means of communication. The seminar will include specific writing techniques, necessary elements, daily on-the-job training, comprehension exercises, and a Q&A session. *For details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a practical and hands-on course that covers the effectiveness audit in ISO 9001 internal audits, including the concept of effectiveness audits, how to create checklists, how to ask questions, criteria for determining nonconformities, and how to prepare audit reports, all through exercises. It will address how to conduct internal audits, how to carry out effectiveness audits, process approach effectiveness audits, and exercises on creating audit checklists based on descriptions of manufacturing processes. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar aims to understand the mechanisms of EMI generation that pose problems in EMC design and the principles of EMS reduction, with the goal of acquiring knowledge to implement designs that are less likely to cause EMC issues from the early stages of product development. Topics covered include resonance, electrostatic induction, electromagnetic induction and shielding, antennas, differential mode/common mode and radiated electric fields, EMC countermeasure components, EMC design, and examples of SPICE simulation. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain water electrolysis technology for producing green hydrogen, focusing on low-temperature water electrolysis methods. It will cover the basics of electrochemistry necessary to understand water electrolysis, the fundamentals of water electrolysis, the basic principles and research and development trends of various water electrolysis methods, recent research and development trends both domestically and internationally, and the challenges of water electrolysis. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course designed to understand transmission line theory using LTspice and to learn the basics of signal and power integrity design and analysis. It covers transmission line theory, coplanar transmission lines, microstrip differential transmission line design, transient analysis, AC analysis, and FFT analysis using SPICE, current paths in printed circuit boards, driver model creation, and SiPi simulations using various models. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will cover data-driven chemistry aimed at the research and development of new molecular structures and materials, the planning of production processes, and process monitoring and control. We will learn a holistic approach that incorporates process conditions into correlation models of material properties and structure/composition, covering material design, process condition examination, and quality control, through examples from process informatics, soft sensors, and polymer alloy design. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course to learn the basic characteristics of electronic components and how to effectively use LTspice. It quantitatively explains the basic characteristics of inductors (L), capacitors (C), and MOSFETs using formulas, and conducts transient analysis, AC analysis, and FFT analysis. It covers the frequency characteristics of L and C, the channel length, width, threshold, and temperature dependence of CMOS ICs, the use of voltage sources and current sources, as well as the compact, behavioral, S-parameter, and IBIS models of MOSFETs, the library creation of SPICE models, and how to utilize measures and raw files. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a practical workshop led by professional writers and editors, aimed at acquiring direction and editing skills on how to effectively utilize and communicate with AI. It covers the characteristics of generative AI, the mindset for AI writing, the article production flow, web articles, copy and catchphrases, public relations and social media, and the approach to information dissemination in the AI era. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will explain the meaning of the requirements of the ISO 9001 standard, and how to apply it as a quality management system that fits the characteristics and actual conditions of a company, through practical examples. It will cover an overview of the ISO 9000 family of standards, the structure and key points of the ISO 9001:2015 standard, the implications of the requirements in Chapters 4 to 10 of ISO 9001, as well as considerations and practical examples of application. *For more details, please check the related links or the seminar details in the catalog.

• Technical Seminar

This seminar will explain the current state of data sharing and utilization in R&D departments, as well as the causes and issues arising from the accumulation of person-dependent data. It will cover methods for achieving data sharing, data accumulation and operation with a focus on data exploration and analysis, ways to incorporate AI and machine learning into actual experimental research, and the challenges and countermeasures for maintaining and expanding the integration and operation of databases and machine learning, using concrete examples. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will introduce the mechanisms and systems of next-generation vehicles, focusing on the cutting-edge technologies of the era of autonomous driving and electric vehicles. We will cover the mechanisms and systems actually used in automobiles, the effectiveness of next-generation automotive mechanisms, the individual functions that make up advanced mechanisms, the evolving driving mechanisms, the state-of-the-art technologies that control vehicle motion, the mechanisms of autonomous driving, and the latest information from automobile manufacturers. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar will systematically explain extracellular vesicles (EVs), including exosomes, covering domestic and international market trends, regulatory environments, industrial manufacturing methods, quality assessment, applications in liquid biopsy, and next-generation exosome technologies. It will address the definition, classification, and functions of exosomes, industry and market trends, applications and business opportunities, regulatory environments and quality control, industrial manufacturing methods, quality assessment and standardization, business models, and industry outlook. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is an introductory technical course aimed at those who have no prior experience in building immunological measurement systems, while considering the use of biomarkers in biological samples at various stages of drug discovery research. It will explain the significance of biomarkers in drug development, exploration methods, specificity confirmation, immunological measurement methods, performance evaluation of measurement systems, specific evaluation cases, and the development of companion diagnostics. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar covers the effectiveness audit in ISO 9001 internal audits, including the concept of effectiveness audits, how to create checklists, how to ask questions, criteria for determining nonconformities, and how to prepare audit reports, all through practical exercises. It will address how to conduct internal audits, how to carry out effectiveness audits, process approach effectiveness audits, and the creation of audit checklists based on the description of manufacturing process conditions.

• Technical Seminar

This seminar is aimed at those who have recently been assigned to departments related to pharmaceutical GMP or those who are responsible for businesses related to pharmaceutical manufacturing, even if they are not part of a pharmaceutical company. It will explain what the regulations that must be complied with (GMP) require and what their purpose is. The seminar will cover the basic matters of GMP regulations necessary to grasp the overall picture of GMP, including pharmaceuticals, Japan's legal system and GMP, the origins of GMP, GMP compliance inspections, and the management tasks stipulated by GMP regulations. *For more details, please check the related links or the seminar details in the catalog.*

• Technical Seminar

This seminar is a course that organizes practical thinking about "gray zone quality" in biopharmaceuticals such as antibody drugs, regenerative medicine products, and nucleic acid drugs, which cannot be judged solely by GMP and standards/procedures. It explains the differences between scientific rationality and regulatory rationality in situations where manufacturing results and quality data cannot be clearly defined, the roles of GMP documents and CTD (Module 3), and the differences in judgment among departments such as QA, CMC, research, and clinical. Participants will learn to view quality judgment as a responsibility of the entire company rather than just individuals, and will acquire perspectives that can be utilized for explainable judgment criteria and medium- to long-term quality strategies.

• Technical Seminar

We offer a translation service called 'Chinese Translation PRO,' which boasts industry-leading achievements. Our team mainly consists of individuals with study abroad experience in science and engineering graduate schools in Japan and Western countries, as well as those who have been involved in advanced technology research and development at Japanese and Western companies, focusing on the translation of technical documents such as patents. Additionally, we have implemented an advanced translation management system that includes tool-based checks, terminology unification, and the construction of client-specific specialized dictionaries, all aimed at maintaining high and stable quality. **Features** - Overwhelming achievements that are top-class in the industry - Translators with a level that sets us apart from other companies - Reliable quality management system *For more details, please download the PDF or feel free to contact us.*

• Translation/Interpretation

When considering the Chinese character representation of products and services for business development in China, it is important to note that the meanings of kanji can differ between Japanese and Chinese. Our naming service offers three suggested Chinese names (in kanji) that are deemed suitable by native brand naming specialists, while conducting prior trademark searches to avoid similarities. When making our suggestions, we will also report on the pronunciation, meaning, and reasons for selection of the trademark name (Chinese kanji representation), which can serve as a reference for your trademark selection process. 【Features】 ■ Proposing three naming options (kanji representation) while conducting prior trademark searches ■ Reporting on the pronunciation, meaning, and reasons for selection of the trademark name (Chinese kanji representation) ■ Can be used as a reference for trademark selection work *For more details, please refer to the PDF materials or feel free to contact us.

• Other contract services

At Japan I.R., we offer a "China Trademark Survey" service, which includes a research report detailing comments in Japanese on the extracted prior trademarks. When manufacturing and selling products or services in China under a trademark, it is necessary to conduct a preliminary investigation to ensure that you are not infringing on others' trademark rights, regardless of whether you plan to file an application yourself. Naturally, trademark infringement in China can lead to injunctions and claims for damages, which can cause significant harm to business operations. It is also important to conduct a prior trademark search at the time of application. If there are existing prior trademarks, the application may be rejected, resulting in wasted application costs. [Services Offered] ■ Trademark Search (Word Marks) ■ Trademark Search (Design Marks) *For more details, please refer to the PDF materials or feel free to contact us.

• Other contract services

At Japan IR, we provide services entirely in Japanese, from pre-application guidance, application preparation, intermediate processing, to registration, allowing for smooth communication even with complex procedures. In China, comprehensive designations of goods and services and the description of class headings are not permitted, requiring careful judgment. We also support the description (designation) methods and expressions for designated goods, so please rest assured. Additionally, our company achieves extremely high cost performance by having professionals in Chinese trademark practice who are fluent in Japanese handle everything in a one-stop manner. 【Features】 ■ Quick and accurate response ■ Achieving overwhelming cost performance ■ Providing all services in Japanese ■ One-stop support by professionals in Chinese trademark practice who are fluent in Japanese *For more details, please refer to the PDF materials or feel free to contact us.

• Other contract services

The Japan IR Corporation's comprehensive catalog for Chinese trademarks introduces the "Total Solution for Chinese Trademarks," which supports Chinese trademark strategies quickly and accurately. It features "Chinese Trademark Applications" that achieve rapid and precise responses with overwhelming cost performance, "Chinese Trademark Investigations" that deliver high-precision research results, and "Chinese Trademark Watching (SDI)" that emphasizes the importance of early responses through regular monitoring, among many others. 【Featured Products】 ■ Chinese Trademark Applications ■ Chinese Trademark Investigations ■ Chinese Trademark Watching (SDI) ■ Chinese Trademark Naming Services ■ Designated Goods Compliance Check Service, etc. *For more details, please contact us or download the catalog.

• Patent/Copyright related services
• Translation/Interpretation

In this course, we will introduce the basics of rapidly advancing vacuum technology and thin film technology, as well as the principles of various thin film techniques. We will explain important points from thin film design to quality enhancement and defect countermeasures. In the public session, we will present the latest application examples of thin film technology, focusing on fields that are expected to gain attention in the future, such as medical devices, home appliances, building materials, automobiles, and aerospace, along with explanations of the technical principles. The application areas are expanding endlessly, including the substitution of plastics for metals and glass, the addition of surface functions through biomimetics, and the use of thin film potentials, sensors, and devices in IoT. We hope you find this information useful for the development and utilization of thin film technology, which is essential for manufacturing in the new era.

• Technical Seminar

Revolutionary low cost starting from 9,800 yen per month at one company! The educational content of Japan IR, which continues to be utilized by many large corporations, is created with a focus on friendliness and clarity, using a lot of illustrations. The course content can be switched on a monthly basis upon request from the education personnel. By dynamically selecting learning content according to your company's intellectual property education plan, you can continuously utilize e-learning without waste and at a low cost. Furthermore, customization of the courses is also possible. By using content tailored specifically for your company that reflects internal circumstances, even more effective education can be achieved.

• Distance learning/E-learning
• Patent/Copyright related services