サイエンス＆テクノロジー List of Products and Services

A book compiled over three years by Hirodo Noguchi, who has been active at Dai Nippon Ink and Chemicals and Canon, and is currently working as a consultant! This book explains recent technological trends based on the author's research data, published literature, and patent literature, covering approximately 900 pages, and serves as a valuable resource for gaining a broad and deep understanding of inkjet (IJ) printing. In Part 1, "The Diverse Forms of Inkjet Printing," readers can understand that IJ printing encompasses a wide range of printing targets and multiple ink types, leading to the emergence of various distinctive printers. In Part 2, "Phenomena and Solutions of Troubles," readers can grasp how head and printer designers confront ink to achieve the intended image formation. Part 3, "Image Quality, Process Control, and Ink Technology," explains the drying methods and materials for water-based inks, the acceleration of printing, and the surfactant technologies that support dot formation. Part 4, "Applications of Ink and Printers," examines recent examples of new printer products and the roles played by inks, based on published literature and related invention documents. Additionally, it includes discussions on the application trends of "IJ dyeing," which is expected to develop further, as well as introductions to technologies and products in various industrial printing fields.

• Technical and Reference Books

◆Explaining the technological trends towards the high performance of LiB and the trends in the electric vehicle and automotive battery industry <Technical Explanation Section> ▼Possibilities and challenges of LiB ▼Trends in various electrode materials and electrode slurry manufacturing technologies <Industry Trends Section> ▼The electrification route gaining momentum in response to regulations and the future strategies of major automobile manufacturers ▼Impacts of China's subsidy policies and revisions to NEV regulations ▼Investment status of LiB companies and their connections with vehicle manufacturers, the power dynamics since 2020 ▼Trends of Chinese battery-related companies

• Technical and Reference Books

【Book + eBook】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/22452.html ～What PIC/S inspectors noted during the joint workshop with PDA regarding API GMP inspections～ ～We will convey the insights of European (EMA) inspectors, who are said to have limited information, through "live" comments～ 【This book has been officially authorized by PIC/S for translation and publication】 What is AIDE MEMOIRE… It is a manual created to assist inspectors from PIC/S member countries during GMP inspections. At the joint workshop held in May 2012 in Geneva, Switzerland, between European PDA and inspectors from PIC/S member countries, numerous comments and recommendations were made by inspectors from EU countries regarding issues related to API inspections! The author, who is well-versed in inspections in the three regions, has included respective countermeasures alongside the translation of "API Facility Inspection (PI 030-1)"!

• Technical and Reference Books

【eBook version】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/27312.html *No application download is required for the Word format. (Membership registration is necessary) 【Downloadable SOP Word Data】 *Our company cannot be held responsible for any troubles or issues arising from the use of this format data. Please use it at your own risk. ● SOP format for the foundation of GMP-SOP ● SOP format for CAPA ● SOP format for deviation management ● SOP format for laboratory management ● SOP format for cleaning methods ● SOP format for clean rooms ● SOP format for pharmaceutical packaging ● SOP format for maintenance inspection management ● SOP format for supplier management ● SOP format for shipping determination, recalls, and complaint handling

• Technical and Reference Books

【Book + eBook】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/22196.html 【Comprehensive Guide to Microorganisms in Pharmaceuticals】 "Microorganisms that are Beneficial and Harmful" Unraveling the roles and issues of pharmaceuticals and microorganisms that are inextricably linked Natural product drug discovery methods and considerations for generic production, looking ahead to active pharmaceutical ingredient production Microbial management in laboratories/manufacturing sites compliant with PIC/S - Deviations/Alerts, Actions, Monitoring - ■ Considerations for natural product drug discovery aimed at new drug and generic development Are there really no useful microorganisms left that could become new drugs... What should be known at the development stage with an eye on the manufacturing line... The microorganisms involved in past pharmaceutical development and those currently being developed... ■ Considerations for microbial management in laboratories/manufacturing sites compliant with PIC/S What is microbial testing management and how to handle re-testing/validation... What are the environmental monitoring methods that comply with the three pharmacopoeias/GMP... What are the alert/action levels and deviation responses in microbial management...

• Technical and Reference Books

【Book + eBook】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/21523.html You can read this popular product at this price only in eBook format! The format is highly praised by monitors and CRCs for its usability in actual fieldwork! For those who find themselves spending too much time on document preparation due to "reconfirmation and revisits due to errors," we present a collection of formats to efficiently reduce workload. <Preventing excessive or insufficient documentation for each item such as protocols, consent forms, and clinical trial summary reports> - Guidelines for protocol creation compared to J-GCP / precise regulatory methods to prevent deviations - Differences in documentation methods between company-led and physician-led studies and materials for addressing each - How to address matters not typically covered in regular medical practice for physician-led clinical trials and the necessary organizational structure 【Pharmaceuticals Edition】 <Included Formats> - Investigational Drug Brochure - Clinical Trial Protocol - Informed Consent Document 【Medical Devices Edition】 <Included Formats> - Clinical Trial Protocol - Case Report Form - Informed Consent Form - Investigational Device Brochure - Clinical Trial Summary Report

• Technical and Reference Books

【Book + eBook】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/21019.html "Global GMP Requirements and Inspection Responses Interpreted from the PIC/S Inspector Manual" 【This book is officially authorized by PIC/S for translation and publication】 Understanding the intent of questions from the PIC/S Inspector Manual, and what responses and methods inspectors expect. Alongside the translation of the current QA personnel's "AIDE MEMOIRE ON ASSESSMENT OF QRM IMPLEMENTATION," we explore what PIC/S inspectors look for and require. This is a translation of PIC/S GMP compliance methods by active personnel. Contents: Introduction of risk management required by PIC/S GMP, considering quality risk management in ICH Q9 and Q10 - Quality risk management for manufacturing/equipment/utilities - Quality risk management as part of material management - Quality risk management as part of production

• Technical and Reference Books

★ The positioning of the first edition concept "Textbook of LCM Strategy" remains unchanged, with a complete revision to the latest perspectives! ★ New chapters on "Biopharmaceuticals," "BD Drug Discovery, Databases, and AI Drug Discovery," and "LCM/DR Pricing Strategies" have been established! ～≪Eye-opening! Common sense has been overturned!≫ A textbook on pharmaceutical lifecycle strategies that interprets case studies from a comprehensive perspective. ■ Point 1: The concept of the previous edition, which was well-received, maintains its position as a "textbook" in LCM strategy! Significantly enhanced with a large addition of case studies!!! ■ Point 2: Detailed discussion on LCM and DR utilizing artificial intelligence (AI), which was not covered in the first edition! ■ Point 3: Policies and related patent case law for biopharmaceuticals considered from the latest trends. ■ Point 4: Significantly revised based on the latest trends in the field! Explains how to write specifications with consideration for know-how management and patent extensions from the perspective of examiners! ■ Point 5: A new chapter detailing LCM/DR and pricing strategies!

• Technical and Reference Books

【Book】 + 【ebook】 set! With the ebook, you can search quickly! Photos are in full color! This book is available for viewing as an ebook in addition to the printed version. *Ebook viewing is a service for purchasers only (free/1 account). You can view it on up to two devices per person, and you can access it not only on your company PC but also on your tablet via the app during your commute. Ebook downloads are done within the S&T member "My Page," so S&T membership registration (free) is required. [Supported devices] Win and Mac OS, smartphones, and reading devices (iPhone, iPad, etc.) [Format] PDF (viewable through the application "bookend" for content protection) [Number of viewable PCs] 2 devices/1 account (limited to the same account) If you wish to view the ebook, please do the following after purchase: (1) Register using the "ebook viewing application form" enclosed with the book shipment. (2) Fill in the "invoice number," the "company name," "name," and "S&T registered email" of the person viewing, and send it via email.

• Technical and Reference Books

Sealant materials and raw material manufacturers, sealant material manufacturing equipment and sealant process equipment manufacturers To those in charge of development and manufacturing technology at user companies of sealant materials and companies considering new entries— This is a bible that details the past and future of sealant materials along with specific and practical technical information. ■ Expectations for new materials and technologies are rising in semiconductor sealing, entering a transformative era ~From EMC (solid materials and tablet products) to new materials such as inks, films, and powders~ - The emergence of new PKG types such as FO-type packages (PKG) and three-dimensional modules is changing the sealing targets. - The focus is shifting from traditional chips to sealing connection circuits (substrates and rewiring). ■ Thoroughly understand sealant materials! Practical and specific technical information related to the development and manufacturing of sealant materials ~Detailed explanations incorporating the author's experiences, experimental notes, and actual process diagrams~ - The development history of sealant materials in line with the evolution of PKG shapes, mounting methods, and sealing methods. - Requirements for resin sealing methods such as various molding methods, casting, dipping, dripping, and immersion methods. In addition, the "Column" section includes business customs and company information in the semiconductor and sealant material industries, as well as development experiences.

• Technical and Reference Books

【eBook Edition】 For details and applications regarding this product, please check our website. https://www.science-t.com/ebook/EB028.html "Timely" Technical Trend and Needs Catch-Up: "Technical Trend Report" Focusing on themes such as <TFT-LCD>, <OLED>, <MicroLED>, <Quantum Dots/QD LED>, and <Automotive Displays>, we review excellent examples of productization and research and development for each display, as well as trends in materials, components, and manufacturing technologies. Please take a look to grasp the future direction of technology and business development! ▼Keywords covered in this book▼ ● Challenges and prospects of new display technologies discussed at SID2019, examined from both technical and business perspectives. The keynote speech review introduces presentations from Samsung, Google, and BOE. ● Review of evolving LCD element technologies. ● Review of the latest OLED technologies. ● Development of MicroLEDs progressing towards practical application. ● Insights on Quantum Dots and QD LED. ● Automotive technology as a new focus application for displays.

• Technical and Reference Books

【Book + eBook】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/EB029a.html The highly acclaimed book is now available in digital format! Downloadable on up to 10 devices. ~Set version of Book + eBook~ A technical specialty book that can be read on smartphones and tablets during overseas business trips, commutes, or meetings, designed for multiple users*【eBook (electronic book)】 *5 accounts: Up to 2 devices per account *This product is a set version of the book + eBook. ~Science & Technology eBook (electronic book)~ ✔ Once downloaded, it can be viewed offline, making it accessible even while overseas or on business trips. ✔ Since up to 2 devices can be downloaded per person, you can view it on both your work PC and personal tablet by downloading the app. ✔ It can be viewed by up to 5 people (5 accounts), allowing for sharing within departments. ✔ If you change your PC, you can re-download it from the web page.

• Technical and Reference Books

【eBook Version】 For details and applications for this product, please check our website. https://www.science-t.com/ebook/EB029.html The highly acclaimed book is now available in electronic version! Downloadable on up to 10 devices. Whether on a business trip, during your commute, or at a meeting, you can read this multi-user viewing technical book on your smartphone or tablet【eBook (electronic book)】. *5 accounts: Up to 2 devices per account allowed. ~This product is the standalone eBook version. There is a special set price available when purchased together with the printed version.~ ~Science & Technology eBook (electronic book)~ ✔ Once downloaded, it can be viewed offline, making it accessible even while abroad or on business trips. ✔ Since up to 2 devices can be downloaded per person, you can view it on both your work PC and personal tablet by downloading the app. ✔ It can be viewed by up to 5 people (5 accounts), allowing for sharing within departments. ✔ If you change your PC, you can re-download it from the web page.

• Technical and Reference Books

A collection of corporate experiences and wisdom viewed through the lens of "technology transfer"! This book is beneficial not only for practitioners involved in technology transfer but also for management overseeing operations and government officials! <Key Points of This Book> ✔ What are the challenges and organizational strategies for addressing technology transfer from the perspective of the QbD approach and ICH Q12 (pharmaceutical lifecycle)? ✔ What should be done, when, and to what extent? What development strategies change at different stages of development for successful technology transfer? This book explains technology transfer in active pharmaceutical ingredient and formulation development based on actual case studies from the perspective of ensuring equivalence! ✔ Diversifying manufacturing outsourcing to domestic and international CMOs... What are the selection and management processes for outsourcing partners, actual trouble cases that arise, and the various responses required by overseas authorities for each manufacturing CMO? ✔ As manufacturing outsourcing becomes common in biopharmaceuticals and antibody drugs, what are the key points for establishing an outsourcing system to ensure production as intended?

• Technical and Reference Books

<<Key Points of This Book>> ■ The Status of Prefilled Syringes in the Medical Market Challenges of Self-Administration and GMP & QMS Management in Medical Product Manufacturing ■ Standard Testing of Prefilled Syringes in Japan, Europe, and the U.S. ~Current Situation and Differences in Pharmaceutical Regulatory Harmonization~ ■ Challenges to Consider and Required Quality Components for Prefilled Biopharmaceuticals ~Specific Development Examples from the Perspective of Syringe Manufacturing~ ■ Required Container Materials and Packaging Design Flow for Syringe Materials ~Basic Requirements and Adaptation to Drug Properties~ ■ Development Case of the Antibody Drug Actemra ~Post-Marketing - Appropriate Use and Actual Complaint Reporting~ ■ Points of Ease of Use and Areas for Improvement of Prefilled Kit Formulations from a Physician's Perspective ~How to Recognize Mistakes and Prevent Errors~ ■ Mechanisms of Aggregate Formation in Biopharmaceuticals and Key Points for Suppression ~Towards Stabilization of Formulations~ ■ Minimization of Aggregates in Biopharmaceuticals ~Introduction of Existing Technologies for Aggregate Removal and Suppression in Antibody Drugs, and Development Trends of New Aggregate Removal/Suppression Technologies~ ■ Understanding and Controlling Antibody Aggregation Mechanisms for the Purpose of Building Bioprocesses (Antibody Production CHO Cell Lines) ~Examples of Protein Aggregation~

• Technical and Reference Books

✔ Address the wave of significant transformations such as electrification and autonomous driving, the entry of companies from different industries, and this period of major change not seen in 100 years! ✔ Gain an overview and understanding of the current state and future trends of powertrain-related technologies, the heart of the automobile! ✔ Towards future business developments for the automotive industry and automotive-related companies.

• Technical and Reference Books

In EU pharmacovigilance operations, the establishment of a quality system based on Module I is mandatory; however, many organizations still lack sufficient implementation and development of such systems. This document explains the fundamental understanding of ISO 9001 and Module I, as well as the actual process construction and operation, audits, and CAPA responses, based on a process approach! It is a recommended read for everyone involved in global PV operations. ■ Key points of this document: 【1】 The explanation is structured along the flow of practical work, making it easy for beginners to understand! Written by an author with many years of experience in PV operations and training at major pharmaceutical companies, this is a textbook on quality systems in PV. 【2】 It complements deficiencies using ISO 9001, which is consistent with Module I. 【3】 PV audits and CAPA responses: ■ In PV audits conducted by organizations independent of the PV department, it is required to possess the capability to evaluate the effectiveness and performance of the system and processes. ■ In reality, there are still many cases where there are issues with root cause analysis, impact assessment, and the content of CAPA.

• Technical and Reference Books

With the advanced development of electrical and electronic devices, various problems caused by heat generated internally have become apparent. As a powerful measure to address these issues, efforts are being made to impart thermal conductivity to rubber, plastics, adhesives, and greases, allowing heat to dissipate outside the system. Originally, polymers possess an inherent property that hinders thermal conductivity. Bestowing thermal conductivity to their compositions presents a significant challenge and is also a battle against high technical difficulties. As part of addressing this issue, a seminar titled "Eye-Opening Thermal Conductive Compositions Design Guide" was held in November 2011, attracting numerous participants. Following the seminar, questions and consultations continued, leading to the planning of this lecture transcript as a technical document that can be referenced on demand. The lecture transcript includes parts that could not be explained in detail during the seminar due to time constraints, as well as sections that were omitted from the program, all newly drafted and incorporated. It is structured to enable understanding and confirmation of all technical elements, from formulation design and manufacturing technology to thermal conductivity measurement and theoretical considerations.

• Technical and Reference Books

Thermal Management and Air Conditioning Systems for Improved Fuel Efficiency and Comfort ~ A Comprehensive Explanation from Both Practical Technology and R&D Perspectives ~ ✔ Insulation technology for engine parts and engine rooms to reduce heat loss and enable quick warm-up ✔ Air conditioning technologies such as thermal storage heating and heat-driven refrigeration cycles to reduce air conditioning energy ✔ Power and energy recovery technologies from waste heat ✔ Requirements for cooling systems for each power source and heat exchanger technologies such as EGR coolers, intercoolers, condensers, and radiators ✔ Overview of air conditioning systems for each power source and trends in technologies such as heat pumps, heating elements, and CO2 refrigerant air conditioners ✔ Energy-saving air conditioning through interior and exterior materials like glass interlayers, heat-shielding and infrared-reflective films, reflective paints, and seat heaters ✔ Cooling technologies for PCUs, motors, and battery systems, which are increasingly required due to electrification ✔ Thermal management and air conditioning control required for autonomous vehicles that are becoming closer to living spaces, along with improvements in comfort We will deliver a wealth of technical information in a volume exceeding 500 pages!

• Technical and Reference Books

There are few clear regulations regarding the manufacturing and quality control of non-sterile pharmaceuticals... To what extent is it necessary to respond? Approaching that gray area!! ✔ Frequency of monitoring, examples of deviation handling ✔ Risk-based approach to contamination control in the manufacturing of non-sterile pharmaceuticals ~ Management of environmental monitoring in non-sterile manufacturing areas (frequency, acceptance criteria) according to USP <1115> ✔ Handling of deviations ~ Guidance from the ECA Pharmaceutical Microbiology Working Group ✔ Microbial monitoring of pharmaceutical water - Standards and testing methods for microorganisms in pharmaceutical water ✔ Necessary levels of microbial control for non-sterile pharmaceuticals and considerations for validation and implementation of microbial limit testing methods ✔ Operational examples and case studies of microbial limit testing for non-sterile products (formulations, pharmaceutical raw materials) ~ Points to consider for each dosage form (powder, liquid, ointment, tablet, capsule, aerosol, transdermal patch) ✔ Implementation methods and application examples of rapid microbial testing methods in manufacturing environments (airborne bacteria) (pharmaceutical water) ✔ Development and reconstruction methods for foreign matter and insect management programs in non-sterile manufacturing areas, along with training examples.

• Technical and Reference Books

Deepen your understanding with behind-the-scenes stories from case studies in the book! Topics include: 【Biopharmaceuticals】【AI Drug Discovery】【Drug Repositioning Case Studies】【Drug Pricing Strategies】, etc... Get the inside scoop on new items and numerous additional case studies in the book! You can only hear this here! Behind-the-scenes stories and anecdotes that can't be written in the book, and raw stories unique to the seminar! ✔ Researchers will take the "lead" with plenty of ideas and hints for proposing LCM and DR ✔ Learn from the latest industry trends and business models, including 【AI Drug Discovery】【DR】【Biopharmaceuticals】【Drug Pricing Strategies】 ✔ How to write specifications considering know-how management and patent extensions In celebration of the release of the fully revised edition of our highly acclaimed book "LCM Extension Strategy Case Studies/Precedents," which has been updated for the first time in four years, we have decided to hold a commemorative lecture! Published in February 2019 '【Fully Revised Edition】 Behind the Scenes of Pharmaceutical LCM Extension Strategy Case Studies and Precedents, and Overlooked Gaps in Rights Acquisition' ◎ Over 200 rich case studies/data on various companies' LCM strategies and their explanations ◎ Responding to the latest industry trends such as biopharmaceuticals, AI drug discovery, drug repositioning case studies, and drug pricing strategies *Purchasers of the book will receive special benefits when attending this seminar. Please contact us for details.

• Technical Seminar

◆The first introductory book explaining the basics and principles of polarizers and phase difference plates, as well as industrial technologies◆ ◆For beginners, those who will be engaged in the field of optical films, and for those looking to reaffirm their fundamentals◆ ● What are the properties of light and what is polarization? How do polarizers and phase difference plates work? ● What basic performance is required of polarizers and phase difference plates, and what technologies support them? ● How are polarizers and phase difference plates manufactured? ● Materials that make up polarizers and phase difference plates, such as PVA, TAC, PET films, and adhesives ● Various types and characteristics of polarizers and phase difference plates, and the essential technologies for functionalization ● The roles of polarizers and phase difference plates in various applications, including LCDs, and the evolution process... etc. You can learn the necessary foundational knowledge for developing functional films in line with the evolution of displays.

• Technical and Reference Books

This book explains and presents case studies based on the authors' experiences regarding approaches to risk. Please use the cases introduced here as a reference to prevent omissions in risk when implementing them in your own company. # Points raised in inspections related to risk management # Are you unsure about how to specifically confront risks? # Have you been conducting risk assessments until now? # Understanding of risk, sharing within the company, and the quality of risk assessments.

• Technical and Reference Books