We have compiled a list of manufacturers, distributors, product information, reference prices, and rankings for Authentication Services.
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Authentication Services Product List and Ranking from 34 Manufacturers, Suppliers and Companies

Last Updated: Aggregation Period:Nov 19, 2025~Dec 16, 2025
This ranking is based on the number of page views on our site.

Authentication Services Manufacturer, Suppliers and Company Rankings

Last Updated: Aggregation Period:Nov 19, 2025~Dec 16, 2025
This ranking is based on the number of page views on our site.

  1. UL Japan Tokyo//Testing, Analysis and Measurement
  2. null/null
  3. ドイツ品質システム認証 Tokyo//others
  4. 4 メトラー・トレド Tokyo//Testing, Analysis and Measurement
  5. 5 マーケットリサーチセンター Tokyo//Service Industry

Authentication Services Product ranking

Last Updated: Aggregation Period:Nov 19, 2025~Dec 16, 2025
This ranking is based on the number of page views on our site.

  1. Support for obtaining PSE/PSC/S marks UL Japan
  2. [Data] List of Radio Laws by Country for Wireless Devices (Excerpt) UL Japan
  3. China ROHS and CQC Mark Certification Services (Voluntary Product Certification)
  4. 4 Booklet "Q&A on Safety Standards for Laser Products" UL Japan
  5. 5 Calibration, verification, certification services メトラー・トレド

Authentication Services Product List

16~30 item / All 88 items

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Comparison of SSO and IDaaS

The difference between "SSO" and "IDaaS"! Introducing the benefits of implementation and recommended services.

In recent years, the number of people using multiple web services and applications for both business and personal purposes has increased. The emergence of diverse services has improved convenience, but the one significant drawback has been the hassle of logging in. This issue has been resolved by SSO (Single Sign-On) and IDaaS (Identity as a Service). So, what exactly are SSO and IDaaS? Additionally, what are the specific benefits of implementing them? In this article, we will compare SSO and IDaaS, and introduce their advantages and recommended services. *For more detailed information, please refer to the related links. Feel free to contact us for further inquiries.*

  • Other security
  • Integrated operation management

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S-JQA Mark Certification: A mark of assurance for electrical products certified by JQA.

The S-JQA mark certification is a comprehensive product safety certification system by JQA for electrical and electronic products.

The third-party certification system operated by the Safety Certification Council for Electrical Appliances (SCEA) certifies products through safety verification testing and quality management inspections of manufacturing facilities. Certified products can display the "S-JQA Mark." 【Features】 ■ All businesses engaged in the manufacturing, importing, or selling of electrical and electronic products, components, etc., both domestically and internationally, can apply. ■ By objectively proving that the certified products meet safety standards as a third-party organization, trust from business partners and consumers is enhanced. ■ By confirming the quality management system of manufacturing facilities, the organization clarifies points for improvement and enhancement of the system. ■ For products covered by the Electrical Appliance and Material Safety Law, it can be used as a self-verification tool by businesses. ■ Compliance assessments are conducted for each product model, and the quality management of the manufacturing facility is verified annually. ■ Compliance assessments are conducted against the technical standards set by the Electrical Appliance and Material Safety Law, and for certain products, certification can be based on additional standards adopted by SCEA or standards such as IEC and JIS. *For more details, please refer to the PDF document or feel free to contact us.

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Obtain certifications from various countries and regions all at once through a single point of contact - International Certification Services.

We propose the optimal application route through our partner overseas organizations to customers who are advancing the acquisition of overseas certifications for electrical products and the like, and we handle the application procedures on their behalf.

We can act on your behalf for the application procedures for safety, EMC, and communication certifications in over 120 countries. You can request the application procedures for certifications in multiple countries and regions all at once. Through our overseas partnership network with certification bodies and testing laboratories in various countries, we can conduct the necessary tests for certifications at our own testing facilities. Additionally, based on commissions from overseas certification bodies, we conduct factory inspections by our inspectors primarily within Japan. We also provide research services on the scope of application and technical standards of certification systems in various countries. 【Features】 ■ Utilizing our unique global network of overseas certification bodies built over many years to support your exports. ■ By utilizing IECEE CB certification for safety and EMC tests, including tests based on standards such as EN, GB, CSA, and UL, obtaining overseas certifications becomes easier. *For more details, please refer to the PDF materials or feel free to contact us.

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Total support for medical device certification and testing

Providing certification required for the manufacturing and sales of medical devices, evaluation and testing related to the safety and quality management of medical devices, and assistance with global certification applications.

We provide total support for our customers in obtaining certifications and evaluating and testing safety and quality, including certification under the Pharmaceuticals and Medical Devices Act for medical devices, various safety assessments, ISO 13485 certification for management systems of manufacturers and distributors, traceability certification for measuring instruments used in medical device manufacturing, and support services for obtaining global certifications for overseas exports. 【Features】 ■ As a registered certification body under the Pharmaceuticals and Medical Devices Act (Registration Number: AH), we conduct certifications for "Highly Controlled Medical Devices" (Class 3) and "Controlled Medical Devices" (Class 2). ■ In safety evaluations of medical devices, we conduct a wide range of product evaluations related to medical devices, including safety testing, Radio Law testing, wireless testing, electromagnetic environment testing, software evaluation, biocompatibility testing, and battery performance testing. ■ We issue valid product evaluation test reports as testing data for compliance with safety standards during certification under the Pharmaceuticals and Medical Devices Act and applications for overseas certifications (test reports can be issued with the ILAC-MRA logo). ■ For home medical devices, in addition to the safety evaluation tests under the Pharmaceuticals and Medical Devices Act mentioned above, we also conduct tests for compliance with technical standards required by the Electrical Appliance and Material Safety Act simultaneously. *For more details, please refer to the PDF materials or feel free to contact us.

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GRIDY Security

Security solutions tailored to our company's security policy!

We would like to introduce our "GRIDY Security." This solution provides an authentication feature called "SAML2.0 Single Sign-On Authentication Service," which allows users to log in to the "Knowledge Suite" with a single ID, as well as an "IP Address Connection Restriction Service" that permits logins only from fixed IP addresses. Please feel free to contact us if you have any inquiries. 【Services Offered】 ■ SAML2.0 Single Sign-On Authentication Service ■ IP Address Connection Restriction Service *For more details, please refer to the related links or feel free to contact us.

  • Software (middle, driver, security, etc.)
  • Other security

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Measures against spoofing emails, specifications for email encryption: What is DMARC?

Explicit processing notification and audit for SPF and DKIM authentication failures!

On our company website, we introduce measures against spoofing emails and the specifications for email encryption. "DMARC" (Domain-based Message Authentication, Reporting & Conformance) is an extension of existing email authentication mechanisms, SPF and DKIM, and is a protocol specification that provides email domain owners with the ability to prevent spoofed email sending. We will provide detailed information about the three major roles of DMARC in the related links. Please take a look. [Contents] ■ The sending domain specifies the policy for how to handle emails that violate SPF or DKIM ■ Detecting spoofed From addresses (DMARC Alignment) ■ Receiving reports necessary for email auditing *For more details, please refer to the related links. Feel free to contact us for more information.

  • Other server related
  • Other security
  • Server monitoring and network management tools

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PowerDMARC Features: Hosted Service

Instead of directly setting it in DNS, centrally manage various settings on the PowerDMARC portal site!

We would like to introduce the features of the email security service 'PowerDMARC' under MENAInfoSec in the United States. The "hosting service" allows for centralized management from the portal's settings screen by referencing the values on the PowerDMARC side using CNAME, rather than directly rewriting the values of the DNS resource records. Please feel free to contact us if you have any inquiries. 【Features】 ■PowerSPF ■Hosted DKIM ■Hosted DMARC ■PowerBIMI ■PowerMTA-STS *For more details, please refer to the PDF document or feel free to contact us.

  • Other services
  • Other security
  • Other server related

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How to set up DMARC in Office 365?

What is missing from Office 365? A step-by-step guide introduced in the blog.

Microsoft is expanding support for email authentication protocols like DMARC across all email platforms. However, to fully leverage its benefits, it is essential to know how to correctly implement DMARC in Office 365. In recent years, many companies have transitioned to effective and robust cloud-based platforms and hosted email solutions like Office 365. Consequently, cybercriminals have upgraded their malicious techniques to cleverly manipulate the security solutions integrated into these platforms to carry out email fraud. This blog will explain how to set up DMARC in Office 365. [Overview (Partial)] ■ Why set up DMARC in Office 365? ■ Is DMARC really necessary if you are using Office 365? ■ How does DMARC function within Office 365? *For more details, you can view the blog through the related links. Please feel free to contact us for more information.

  • Other information systems
  • Other network tools
  • Other analyses

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[Blog] Is SPF necessary for subdomains?

SPF for each subdomain! We will introduce how to manage SPF for subdomains on the blog.

Unlike DMARC, SPF behaves differently for each subdomain. If you are unsure whether to set up SPF for your subdomains or whether to implement a separate (DMARC) policy for them, this article may be helpful. To summarize briefly, the DMARC policy of a domain is automatically applied to its subdomains. This means that if there is a DMARC record with p=reject published for company.com, emails sent from subdomains like support.company.com or marketing.company.com will inherit the same DMARC policy as the zone apex domain, so there is no need to manually configure individual sp (subdomain policy) DMARC tags. [Overview] ■ How does SPF work with subdomains? ■ Creating SPF records for subdomains ■ Why do subdomains (and domains) need SPF? ■ What is an SPF record? *You can view the detailed content of the blog through the related links. For more information, please feel free to contact us.

  • Other information systems
  • Other network tools
  • Other analyses

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ISO/IEC 27001 2022 Edition Compliance Project Special Service

Certification at a very reasonable price! Applicable for both transition audits and ongoing/renewal audits.

We would like to introduce our "ISO/IEC 27001 2022 Version Compliance Planning Special Service" that we are implementing. The international standard ISO/IEC 27001 (Information Security Management) was revised to its latest version in October 2022. In response to this revision, we are prepared to conduct audits compliant with the 2022 version promptly. As part of our special service period for the 2022 version, starting from January 2023 (end date undecided), we will offer reasonable special pricing for new certification registrations and changes in certification bodies. We encourage you to take this opportunity to consult with us. 【Features】 ■ Issuance of the registration certificate in as little as about 3 weeks ■ Audits based on the 2013 version are also possible ■ Audits conducted within the current audit cycle ■ Transition to the 2022 version must be completed by spring 2025 ■ Transition audits can be either continuation audits or renewal audits for the 2022 version *For more details, please refer to the PDF materials or feel free to contact us.

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Product certification based on the Pharmaceuticals and Medical Devices Act.

Before applying for certification, we offer a preliminary consultation (by appointment, up to approximately 2 hours)! Please feel free to contact us.

We provide product certification based on the Pharmaceuticals and Medical Devices Act. Our company has over 20 years of experience in medical devices and possesses a worldwide network of more than 200 experienced auditors. We also actively participate in standard committees and technical committees. Please download the catalog to view the list of certified product categories. 【Why choose DQS?】 ■ Over 20 years of experience in medical devices ■ Active participation in standard committees and technical committees ■ A worldwide network of more than 200 experienced auditors *For more details, please refer to the PDF materials or feel free to contact us.

  • Other contract services

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[Information] Quality Management System ISO 9001

Reduction of management costs and improvement of profit margins through increased productivity and reduced defect rates! Introduction of benefits obtained, etc.

ISO 9001 is a widely recognized international standard for quality management systems. It aims to establish an effective quality management framework and promote continuous improvement across various industries. Whether it is the quality of processes or the quality of final products, quality is a critical aspect of business management and a key competitive factor against other companies. The principles of quality management help your company focus on purpose-driven, systematic management and the continuous improvement of performance. 【Benefits of Acquisition】 ■ Reduction in management costs and improvement in profit margins through increased productivity and reduced defect rates ■ Enhanced reliability through the introduction of globally recognized global standards, as well as reduced or exempted second-party audits ■ Improved operational efficiency through the standardization of business processes ■ Clarification of responsibilities, authorities, and role divisions ■ Development of the organization through the activation of continuous improvement activities *For more details, please refer to the PDF document or feel free to contact us.

  • ISO certification body

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[Information] Occupational Health and Safety Management System ISO 45001

Improving the reliability of occupational health and safety management! Boosting motivation for employees and others through improvements in the work environment!

ISO 45001 is an internationally recognized standard for the effective management of occupational health and safety (OHS) systems. It recommends the proper identification and management of risks such as accidents, disasters, and surrounding threats, enabling smooth operations. It advocates for an integrated management system that combines with other management systems such as environmental and quality management, continuously improving the effectiveness of overall organizational management, and managing and improving not only current occupational health and safety risks but also future risks. [Benefits of Acquisition (Partial)] - Improvement in the reliability of occupational health and safety management - Reduction of risks related to safety in the workplace: self and disaster occurrence, and mental health issues such as depression - Increased motivation of employees through improved working conditions - Enhanced business performance through improved working conditions *For more details, please refer to the PDF document or feel free to contact us.

  • ISO certification body

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[Information] Medical Device Quality Management System ISO 13485

Advantage in new market entry and overseas exports due to international standards! Introduction of benefits of acquisition, etc.

ISO 13485 is the international standard for medical device quality management systems. Companies that belong to one or more stages of the entire lifecycle of medical devices, from design and manufacturing to disposal, are eligible for certification. DQS Japan provides audit and registration services from the customer's perspective, keeping in mind that "there are as many systems as there are organizations," allowing management to determine whether the management system is truly beneficial within the organization. 【Benefits of Acquisition (Excerpt)】 ■ Competitive advantage in new market entry and overseas exports due to international standards ■ Increased trust from the market and customers, improved customer satisfaction ■ Contribution to employee awareness and corporate culture improvement ■ Standardization and clarification of work, enhanced sense of achievement in operations ■ Compliance with laws and regulations, enabling more accurate risk analysis *For more details, please refer to the PDF document or feel free to contact us.

  • ISO certification body

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