ベリフィケーションテクノロジー Product Lineup

This document summarizes our cybersecurity services in accordance with ISO/SAE 21434. It includes the necessity of compliance with ISO/SAE 21434, features of the standard, and a diagram of the standard's structure. You can also check the details of our services, including support for implementation through seminars, threat analysis and risk assessment, and process development support. 【Contents (partial)】 ■ Necessity of compliance with ISO/SAE 21434 ■ What is the international standard "ISO/SAE 21434"? ■ Diagram of the ISO/SAE 21434 standard structure ■ Vtech's services ■ Support for security implementation ■ Threat analysis and risk assessment (TARA) *For more details, please download the PDF or feel free to contact us.

This document is an informational material regarding a seminar on design specifications and verification specifications. It discusses the importance of specifications in design and verification, as well as efforts to standardize based on over 500 achievements. It introduces the use of specification formats that are useful for preventing "omissions and leaks." [Contents] ■ Importance of specifications in design and verification ■ Efforts in standardization at Vtech ■ Seminar on design specifications and verification specifications *For more details, please download the PDF or feel free to contact us.

This document is a technical material that introduces our company's achievements in the design of real-time image processing circuits and high-speed IF circuits. In addition to examples of contracted design for image processing modules such as image processors for digital cameras and endoscope systems, it includes the contracted design flow from C models. It also contains implementation achievements of high-speed serial IFs such as HDMI 2.0, 12G-SDI, and USB 3.0. 【Contents (partial)】 ■ Real-time image processing requires HW implementation ■ Image processing achievements and design flow ■ Achievements in contracted design of image processing modules ■ Contracted design flow from C models (fixed-point model) ■ Contracted design flow from C models (floating-point model) ■ Implementation achievements of high-speed serial IFs (FPGA) *For more details, please download the PDF or feel free to contact us.

This document is a technical material introducing our company's achievements in building a UVM verification environment. It includes improvements in the quality and efficiency of the verification environment through the introduction of UVM, as well as enhancements in the reusability of the verification environment in 1Chip hierarchical design. You can find practical initiatives for improving reusability and support for HW Emulators. 【Contents (partial)】 ■ Features of UVM ■ Improvements in the quality and efficiency of the verification environment through UVM introduction ■ UVM and 1Chip hierarchical design ■ Importance of verification environment planning ■ Examples of UVM compliance in verification environments and measures for improving reusability ■ Measures for improving the reusability of verification environments (1) *For more details, please download the PDF or feel free to contact us.

This document is a technical material summarizing the functional safety services of Verification Technology Co., Ltd. It covers a wide range of topics, from the basic concepts of functional safety to the structure of the ISO 26262 standard, examples of responses to overall safety management, and examples of responses to development projects. It also introduces numerous achievements in functional safety in LSI development, which can be used as a reference for product development. [Contents (partial)] ■ What is functional safety ■ Response to overall safety management ■ Response to development projects ■ Achievements in functional safety in LSI development ■ Summary *For more details, please download the PDF or feel free to contact us.

This document summarizes the support services for security measures under the Cyber Resilience Act. It includes what manufacturers should do to comply with the CRA, the target classifications, and the technical documents required for the self-EU declaration of conformity. You can also check our support offerings, including GAP analysis, process development support, vulnerability testing, and development support/contracting. [Contents (partial)] ■ What manufacturers should do ■ CRA targets ■ Self-EU declaration of conformity ■ Overview of the product development process for CRA compliance ■ Vtech support services ■ GAP analysis *For more details, please download the PDF or feel free to contact us.

This document is an introduction to the "Integration Compliance Support Service for European Market Regulations (Machinery Directive/CRA/EU AI Act)." It includes the content that manufacturers should implement under the Machinery Directive/CRA/EU AI Act, as well as specific actions in response to the requirements of these regulations. Using security risk assessment as an example, we will also present one example of what we consider to be "specific actions." [Contents] ■ Introduction ■ Content that manufacturers should implement under the Machinery Directive/CRA/EU AI Act ■ Service Overview *For more details, please download the PDF or feel free to contact us.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). In the development of robots and industrial equipment for the EU market, compliance with new regulations such as CE marking and the CRA (Cyber Resilience Act) is required. On the other hand, due to a lack of resources for design and certification compliance, there are often challenges such as delays in development schedules and the need to reassess market launch timings. This document organizes the application timelines and compliance schedules for various regulations and introduces efficient ways to obtain certification. It helps reduce the risks of setbacks and delays in product launches due to regulatory compliance. 【Solutions to Your Concerns】 ■ I want to understand the deadlines for CRA and CE marking compliance. ■ I want to prevent development delays caused by regulatory compliance. ■ I want to proceed with certification compliance with limited design resources. *For more details, please download the PDF. If you have any concerns or issues regarding regulatory compliance, feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). CE marking is the conformity marking required to sell products within the EU. In recent years, the implementation of the Machinery Directive and the Cyber Resilience Act (CRA) has complicated the requirements, necessitating cybersecurity measures and vulnerability management for network-connected devices and AI-equipped products. This document organizes the application schedules and requirements of various regulations, as well as explains practical points for obtaining CE marking. It aims to help reduce the risks of development delays and compliance oversights due to regulatory compliance. 【Solutions to Your Concerns】 ■ I want to understand the deadlines for CE marking and CRA compliance. ■ I want to prevent development delays caused by regulatory compliance. ■ I want to know how to respond to cybersecurity requirements. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The Machinery Directive is a new EU regulation that will be fully applicable from January 20, 2027. With the proliferation of machines utilizing AI and IoT, in addition to traditional safety measures, there is a need to address cybersecurity measures and software update management. Non-compliance can lead to delays in market entry and sales risks, making early preparation crucial. This document explains the requirements and key points of the Machinery Directive and the Cyber Resilience Act (CRA). It offers useful information for practical responses, from risk assessment to the creation of technical documentation. 【Solutions to Your Concerns】 ■ I want to understand the requirements and application schedule of the Machinery Directive. ■ I want to know how to respond to EU regulations, including the CRA. ■ I want to prevent development delays and rework due to regulatory compliance. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The CRA (Cyber Resilience Act) is an EU regulation that requires cybersecurity measures and vulnerability management for products with digital elements from the design stage. Some obligations will begin in 2026, with full application by December 2027. Compliance will require cyber risk assessments, the creation of SBOMs, and the establishment of vulnerability management systems, which poses challenges due to increased workload. This document explains the requirements of the CRA and points for compliance. It introduces practical approaches from risk analysis to technical documentation preparation. 【Solutions to your concerns】 ■ I want to understand the requirements and deadlines of the CRA. ■ I want to know how to respond to SBOM and vulnerability management. ■ I want to advance regulatory compliance despite a lack of design resources. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The European Machinery Directive, which will be applicable from January 2027, requires manufacturers to conduct risk assessments from the design stage and to prepare technical documentation. In particular, for machinery that includes software, the burden of cybersecurity measures and evidence management to demonstrate compliance is increasing. This document explains the key implementation requirements for manufacturers under the Machinery Directive. It also introduces efficient approaches and practical points while considering overlapping requirements with the CRA. 【Solutions to your concerns】 ■ I want to know the requirements for manufacturers under the Machinery Directive. ■ I want to organize responses to EU regulations, including the CRA. ■ I want to reduce the burden on the design department due to regulatory compliance. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The CRA (Cyber Resilience Act) requires manufacturers to conduct cyber risk assessments, create SBOMs (Software Bill of Materials), and establish vulnerability management systems. Additionally, post-market, it is necessary to address vulnerabilities and report incidents, which increases the burden on design and quality assurance departments. This document explains the key requirements for manufacturers under the CRA. It organizes the points of action from pre-market to post-market, providing information that aids in efficient regulatory compliance. [Solutions to your concerns] ■ I want to organize the requirements under the CRA. ■ I want to know how to respond to SBOMs and vulnerability management. ■ I want to advance regulatory compliance with limited resources. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The requirements in the European Machinery Directive, CRA, and EU AI Act are presented on a principle basis, leading to an increasing number of cases where design teams struggle to determine specific response methods. This document introduces practical examples of security risk assessment methods, such as data flow analysis using DFD, threat analysis using STRIDE, and risk verification using Attack Trees. It explains how to translate requirements into concrete actions and provides points for efficiently advancing technical documentation and conformity assessments. 【Solutions to Your Concerns】 ■ Unsure how to implement the requirements of the Machinery Directive, CRA, and EU AI Act ■ Want to know how to conduct security risk assessments and evaluation methods ■ Looking to establish technical documentation and conformity evidence that can withstand audits *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

This document provides a clear explanation of European market regulations (Machinery Directive/CRA/EU AI Act). The EU AI Act requires manufacturers of products classified as high-risk AI systems to implement risk management, data governance, and the preparation of technical documentation. Additionally, there are various practical measures that need to be addressed, such as establishing human oversight, quality management, and post-market monitoring. This document explains the key implementation requirements for manufacturers under the EU AI Act. It also introduces an efficient approach to regulatory compliance, taking into account the relationship with the Machinery Directive and CRA. 【Solutions to Your Concerns】 ■ I want to organize the compliance requirements of the EU AI Act. ■ I want to know how to address high-risk AI systems. ■ I want to advance regulatory compliance, including the Machinery Directive and CRA. *For more details, please download the PDF. If you have any issues or concerns regarding regulatory compliance, please feel free to contact us. We will propose a specific action plan tailored to your company's situation.

In the aerospace field, high-precision and real-time image processing is required for surveillance applications. Particularly in operations in outer space and harsh environments, obtaining and analyzing reliable image data is essential. Detecting subtle changes and understanding extensive situations necessitate advanced image processing technologies and the high-speed interfaces that support them. Our achievements in designing real-time image processing circuits and high-speed IF circuits provide the technological foundation to meet these demands. 【Usage Scenarios】 - Observation and monitoring systems in outer space - Image processing modules mounted on aircraft - Real-time monitoring systems for ground facilities 【Benefits of Implementation】 - Acquisition and analysis of high-precision image data - Real-time situational awareness and rapid response - Improved reliability in harsh environments

In the automotive industry, when introducing products to the European market, compliance with increasingly complex regulations such as the Machinery Directive, the Cyber Resilience Act (CRA), and the EU AI Act is required. In particular, to ensure product safety and market reliability, it is crucial to accurately understand the requirements of these regulations and translate them into specific actions. Our service supports the compliance process with these regulations, helping your products to be smoothly introduced into the European market. 【Use Cases】 - New introduction of automotive parts and systems to the European market - Review of existing products for compliance with European market regulations - Compliance with the Machinery Directive, CRA, and EU AI Act 【Benefits of Implementation】 - Fulfillment of CE marking requirements - Reduction of time to market - Risk reduction through regulatory compliance

In the railway industry’s operation control systems, extremely high reliability and safety are required to support the safe movement of people. In particular, system failures can lead to serious accidents, making thorough safety management from the development stage essential. Our functional safety services respond to the stringent demands of the railway industry and support the realization of safe operation control systems. 【Usage Scenarios】 - Safety analysis of operation control systems - Establishment of safety design processes - Compliance with ISO 26262 standards - Utilization of functional safety achievements in LSI development 【Benefits of Implementation】 - Improved overall system safety - Streamlined development processes - Assurance of compliance with standards - Enhanced product reliability

In the aerospace field, particularly in pilot assistance systems, extremely high reliability and safety are required. Malfunctions in the system can lead to serious accidents, making strict adherence to safety standards and thorough verification from the development stage essential. Our functional safety services provide comprehensive solutions to meet the stringent demands specific to the aerospace sector and ensure the safety of products. 【Application Scenarios】 - Safety analysis of pilot assistance systems - Safety design in compliance with ISO26262 standards - Safety verification in development projects - Functional safety measures in LSI development 【Benefits of Implementation】 - Improved product safety - Streamlined development processes - Reliable compliance with regulatory requirements - Development of highly reliable products

To continue exports to Europe, appropriate responses to the CRA and machinery regulations are required. The requirements will be applied in phases, with the following obligations coming into effect on September 11, 2026: - Vulnerability Reporting Obligation - Reporting Obligation for Exploited Vulnerabilities and Major Incidents As the start of application approaches, many companies are facing challenges such as "not knowing where to start" and "lack of internal resources." This document introduces the support content of the **"CRA and Machinery Regulations Emergency Diagnosis Package,"** which diagnoses the current situation and clarifies priorities within **4 to 6 weeks.** Please download the PDF document for more information. *We also accept inquiries regarding regulatory compliance. We will propose specific action plans tailored to your company's situation.*

In the logistics automation industry, appropriate responses to the CRA (Cyber Resilience Act) and machinery regulations are required for continuous exports to the European market. These requirements will be applied in phases, with obligations for vulnerability reporting and reporting of exploited vulnerabilities and significant incidents coming into effect particularly from September 11, 2026. As the start of these applications approaches, many companies face challenges such as "not knowing where to start" and "lack of internal resources." This document introduces the support content of the "CRA and Machinery Regulations Emergency Diagnosis Package," which diagnoses the current situation and clarifies priorities within 4 to 6 weeks. Please download the PDF document to view it. We also accept inquiries regarding regulatory compliance. We will propose a specific action plan tailored to your company's situation. 【Use Cases】 - Exporting products to the European market - Responding to CRA and machinery regulations - Resolving internal resource shortages - Rapid regulatory compliance 【Benefits of Implementation】 - Continuation of exports to Europe - Risk reduction through regulatory compliance - Development of efficient response plans - Support from experts

In the industrial robot industry and its applications, appropriate responses to the CRA (Cyber Resilience Act) and machinery regulations are required for exports to the European market. In particular, ensuring product safety and cybersecurity is crucial for gaining user trust. Inadequate responses may lead to the risk of halting exports of products to the European market. Our "CRA and Machinery Regulations Emergency Diagnosis Package" supports swift and accurate responses to these challenges. 【Usage Scenarios】 - Industrial robot manufacturers planning to export to the European market - Companies wanting to confirm their compliance status with the CRA and machinery regulations - Companies needing expert support due to insufficient internal resources 【Benefits of Implementation】 - Continuation and smooth facilitation of exports to Europe - Risk reduction through regulatory compliance - Improvement in product reliability

In the semiconductor manufacturing equipment industry, appropriate responses to the CRA and Machinery Directive are required for continued exports to the European market. The requirements will be applied in phases, and from September 11, 2026, obligations for vulnerability reporting and reporting of exploited vulnerabilities and significant incidents will come into effect. As the start of application approaches, many companies face challenges such as "not knowing where to start" and "lack of internal resources." This document introduces the support content of the "CRA and Machinery Directive Urgent Diagnosis Package," which diagnoses the current situation and clarifies priorities within 4 to 6 weeks. 【Usage Scenarios】 - Want to continue exporting products to Europe - Have concerns about compliance with the CRA and Machinery Directive - Lack internal resources - Want to clarify the priorities for compliance 【Benefits of Implementation】 - Enables continued exports to Europe - Reduces risks through regulatory compliance - Facilitates rapid understanding of the current situation and development of response plans

In the medical device industry, appropriate responses to the CRA and Machinery Directive are required for the continuous export to the European market. The requirements will be applied in stages, and from September 11, 2026, obligations for vulnerability reporting and reporting of exploited vulnerabilities and serious incidents will come into effect. As the start of application approaches, many companies face challenges such as "not knowing where to start" and "lack of internal resources." This document introduces the support content of the "CRA and Machinery Directive Emergency Diagnosis Package," which diagnoses the current situation and clarifies priorities within 4 to 6 weeks. 【Usage Scenarios】 - Exporting medical devices to Europe - Responding to the CRA and Machinery Directive - Streamlining the certification acquisition process 【Benefits of Implementation】 - Continuation of exports to Europe - Increased reliability through regulatory compliance - Risk reduction through prompt responses