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 32 Manufacturers, Suppliers and Companies

Last Updated： Aggregation Period:Oct 08, 2025～Nov 04, 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:Oct 08, 2025～Nov 04, 2025
This ranking is based on the number of page views on our site.

  1. UL Japan Tokyo//Testing, Analysis and Measurement
  2. Spelldata Tokyo//Information and Communications
  3. ドイツ品質システム認証 Tokyo//others
  4. 4 イニシャル・ポイント Tokyo//IT/Telecommunications
  5. 5 DEKRAサーティフィケーション・ジャパン 医療機器事業部 Tokyo//others
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Authentication Services Product ranking

Last Updated： Aggregation Period:Oct 08, 2025～Nov 04, 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. ISO certification services アームスタンダード
  4. 4 Shot2Play ショットツープレイ
  5. 4 Medical device product safety standards evaluation, testing, and certification services. UL Japan

Authentication Services Product List

46～60 item / All 83 items

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Pharmaceutical application / Review and certification services

Pharmaceutical application / Review and certification services

[Overseas Expansion, Pharmaceutical Application Support] Medical Image Management / Development of Various Hospital Information Systems

Development of various systems such as medical image management systems and hospital information systems, as well as medical software systems that comply with various standards and protocols like DICOM/HL7. Support for the import and export of medical devices related to the Pharmaceutical Affairs Law. Comprehensive support for certification of standards such as KFDA, CE marking, and ISO. A total solution one-stop service to assist customers with "preparation of technical documents, testing requests, applications, and obtaining certifications." *For more details, please download the catalog.

  • ISO-related consultant

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SGS Japan Inc. Medical Device and In Vitro Diagnostic Related Certification Services

SGS Japan Inc. Medical Device and In Vitro Diagnostic Related Certification Services

We have top-class certification achievements within Japan and receive high trust from our customers through a global network of highly specialized auditors.

SGS Japan Co., Ltd. provides certification services related to medical devices and in vitro diagnostic products. As a certification body with a top-class track record in medical device certification globally, we support your company's entry into the medical device market, so please feel free to consult with us. 【Features】 ■ One of the few certification bodies in Japan capable of handling comprehensive medical device standards and regulations ■ Experienced auditing staff ■ Trust and proven results

  • Other contract services

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Managed PKI for IoT - Electronic Certificate and Authentication Service

Managed PKI for IoT - Electronic Certificate and Authentication Service

A customized certification authority that enables mass issuance of certificates for IoT.

"Managed PKI for IoT" is a service that can quickly issue certificates in environments that require a large number of certificates, such as IoT. You can customize the format and validity period of the certificates issued according to the environment in which they will be used. Depending on the price you pay, the speed at which certificates can be issued varies, with a maximum issuance speed of 3,000 certificates per second. [Features] ■Mass issuance of 3,000 certificates per second ■Choice of certificate authority format ■Wide range of maximum validity periods *For more details, please download the PDF or feel free to contact us.

  • Embedded system design service

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ID and access management authentication service 'Entra ID'

ID and access management authentication service 'Entra ID'

Flexible access control with conditional access! Centralized ID management.

We would like to introduce "Azure AD/Intune," which we handle. "Azure AD (Azure Active Directory)" is a cloud-based identity and access management authentication service. It enables improved convenience and security through SSO (Single Sign-On). Additionally, by using it in conjunction with "Intune," you can centralize device management and identity management across various operating systems. As a cloud service, it allows management of devices that are not connected to the internal network via the internet. 【Features】 ■ Integration of passwords for all SaaS applications / Prevention of password leaks during login ■ Enhanced security through device authentication and multi-factor authentication (MFA) along with identity management ■ Management of devices and applications from the cloud on a per-unit basis ■ Usable as a requirement for conditional access *For more details, please refer to the related links or feel free to contact us.

  • Other information systems

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What is an IdP? A clear explanation of its mechanism, role, benefits, and more.

What is an IdP? A clear explanation of its mechanism, role, benefits, and more.

Explaining the differences between IdP and SP, the flow of the authentication process, and the benefits of IdP!

SSO (Single Sign-On) is a system that streamlines the use of cloud services and enhances security. The service used in this system is called IdP. Additionally, the authentication method used by IdP is SAML authentication. So, what exactly are IdP and SAML authentication? In this article, we will clearly explain the overview of IdP and SAML authentication that enable SSO, as well as the flow of authentication. *For detailed content of the column, you can view it through the related links. For more information, please feel free to contact us.*

  • Encryption and authentication
  • Other security

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ISO 13485 Certification Services

ISO 13485 Certification Services

We are a registered certification body that provides ISO 13485 certification services!

We provide certification services for the international standard "ISO 13485," which offers guidelines and tools for establishing an effective quality management system for medical devices and services. It is also possible to combine CE certification as an option. The certificate is typically valid for three years from the date of initial issuance. 【Certification Process】 ■ Stage 1: First Stage Audit ■ Stage 2: Second Stage Audit *For more details, please download the PDF or feel free to contact us.

  • Other quality control and hygiene measures
  • Quality Display
  • Other Consulting Services

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Medical device certification service

Medical device certification service

Certification for "designated management medical devices (19 categories)" and "designated in vitro diagnostic drugs" is possible!

Our company provides "Medical Device Certification Services" as a certification body registered with the Ministry of Health, Labour and Welfare for designated management medical devices and designated in vitro diagnostic drugs. We mainly handle items such as anesthesia and respiratory devices, dental equipment, and medical electrical equipment. Please feel free to contact us first. 【Features】 ■ Highly specialized and experienced staff conduct the reviews ■ Rapid and reliable certification through our unique certification management system (Expedited service consultations are also available) ■ Provision of appropriate certification costs and clear services for customers ■ Capable of conducting electrical safety tests, EMC tests, wireless tests, and biocompatibility tests ■ Initial free consultations available upon request *For more details, please download the PDF or feel free to contact us.

  • Other Consulting Services
  • Other contract services

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Testing, evaluation, certification services

Testing, evaluation, certification services

Testing and evaluation of safety and reliability! Capable of handling high-energy batteries such as lithium-ion batteries for automobiles.

The remarkable proliferation of EVs (electric vehicles), HEVs (hybrid electric vehicles), and PHEVs (plug-in hybrid electric vehicles) has led to a sharp increase in the demand for high-output, high-energy-density drive batteries. To ensure the fundamental safety of batteries and obtain essential data regarding the design of automotive systems and battery packs, performance, reliability, and safety testing are essential. Our company provides a wide range of testing and evaluation services with testing facilities capable of handling high-energy batteries such as lithium-ion batteries for automotive use. Additionally, leveraging our track record in type approval testing for various vehicle components, we support obtaining approvals through testing services compliant with R100 and R136, which are mandatory for vehicles equipped with REESS. *For more details, please refer to the PDF document or feel free to contact us.*

  • Public Testing/Laboratory
  • Other contract services
  • Other services

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Fast examination and certification with minimal customer burden! ISO examination and certification services.

Fast examination and certification with minimal customer burden! ISO examination and certification services.

ISO audit and certification services that can be certified in as little as 3 months! Over 1,000 domestic companies have achieved this! Online consultations/estimates available, and remote audits are also supported.

Our company offers "ISO audit and certification services" for ISO 9001, ISO 14001, and ISO 27001 (ISMS), all of which can be certified in as little as three months. We conduct audits based on practical experience rather than paperwork. The main focus of the audit is on explaining daily operations. Additionally, we do not require the submission of a year's worth of documents before the audit, so there is no rush before the audit. Please feel free to consult us when needed. 【Features】 ■ Fast audits ■ Fast certification ■ Minimal burden on customers ■ Over 11,000 companies worldwide and more than 1,000 companies domestically have achieved certification ■ International mutual recognition agreement system * For more details, please refer to the PDF document or feel free to contact us.

  • Management Seminar

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ISO certification services

ISO certification services

We provide "ISO certification audits" for small and medium-sized enterprises to achieve sustainable growth.

Our company provides services focused on third-party checks through ISO certification audits in our Certification Division. We offer a "Certification Course" with a monthly fee structure, allowing you to maintain ISO certification without strain. We can conduct appropriate audits tailored to the specific circumstances of each customer. Please feel free to contact us if you have any requests. 【What you can do with the Certification Course】 ■ By managing in accordance with international standards related to quality and information security, you can enhance customer trust. ■ By having employees share the same rules and goals in their work, you can improve awareness of work within the company. *For more details, please download the PDF or feel free to contact us.

  • ISO certification body

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Push Notification & QR Authentication Service "Mamoru PUSH"

Push Notification & QR Authentication Service "Mamoru PUSH"

Easy and secure push notification & QR authentication service.

"Mamoru PUSH" is a push notification and QR authentication service that achieves simple yet strong authentication by balancing usability and security. We hold a wide range of unique patents for push notification authentication technologies, including those that require the use of tokens or prior consent from the user for authentication. Please feel free to contact us if you have any inquiries. 【Features】 ■ Balances security and usability ■ Rich functionality ■ Holds a wide range of unique patents for push notification authentication ■ Customizable to accommodate uses not covered by existing features *For more details, please download the PDF or feel free to contact us.

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

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European Medical Device Regulation (EU) 2017/745 (MDR)

European Medical Device Regulation (EU) 2017/745 (MDR)

Entry into further markets made possible! Approval of medical devices for sale or distribution in the European Economic Area.

As of May 26, 2021, the EU Regulation 2017/745 (MDR) has been established to replace the old EU directive on medical devices (93/42/EEC). In terms of content, the MDR differs significantly from the previous EU directives in many aspects. Among the important innovations are the expansion of the scope of application, the specification of minimum content for the creation and maintenance of technical documentation, and the tightening of requirements for clinical evaluation. Additionally, new classification rules have been introduced, including a new class classification for reusable surgical instruments, as well as devices that include software and nanomaterials. [Changes to Regulation (EU) 2017/745 for Medical Device Manufacturers (Partial)] ■ Expansion of the scope of application ■ Specification of minimum content for the creation and maintenance of technical documentation ■ Tightening of requirements for clinical evaluation ■ Introduction of new management procedures for high-risk medical devices ■ Appointment of a person responsible for regulatory compliance (PRRC) ■ Strengthening of requirements for post-market surveillance of medical devices *For more details, please refer to the related links or feel free to contact us.

  • Quality assurance support systems and services

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[MDR Application Reception] European Medical Device Regulation (EU) 2017/745

[MDR Application Reception] European Medical Device Regulation (EU) 2017/745

Timely support for consultations in Japanese! We are currently accepting MDR applications within Japan.

Medical devices for the European market are required to comply with the MDR (EU Regulation 2017/745) instead of the old MDD (EU Directive 93/42/EEC) as of May 26, 2021. Except for low-risk Class I devices, certification by a Notified Body (N.B.) is mandatory for Class Is, Im, Ir, Class IIa, IIb, and Class III medical devices. Our company acts as the Japanese contact point for the DQS Group, providing services for medical device certification based on Japan's Medical Device and In-Vitro Diagnostic Medical Device Act, as well as serving as the Japanese contact for DQS Medizinprodukte, the N.B. for MDR. Please feel free to consult us for more details. 【What DQS Japan Can Do for You】 ■ Provide bridging services between Japanese medical device manufacturers and DQS Medizinprodukte ■ Secure MDR auditors and Regulatory Affairs Managers residing in Japan, ensuring timely responses to inquiries in Japanese *For more details, please refer to the related links or feel free to contact us.

  • Quality assurance support systems and services

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How to Access the Japanese Market with Medical Devices <For Foreign Companies>

How to Access the Japanese Market with Medical Devices <For Foreign Companies>

Helping medical device manufacturers enter the Japanese market! Introducing the medical device approval (certification) steps.

In Japan, the Ministry of Health, Labour and Welfare (MHLW) regulates the manufacturing, sales, and distribution of medical devices. Medical device approval (certification) requires steps such as "application" and "QMS conformity assessment." Additionally, all application documents and technical documentation must be prepared in Japanese. The DQS Group can assist manufacturers of medical devices entering the Japanese market by dividing roles, so please feel free to contact us when needed. 【Medical Device Approval Steps (Partial)】 ■ Search for the general name of the medical device for which approval is sought, and examine the approval criteria and the status of existing devices in Japan to consider application methods and identify technical issues. ■ Select the applicant (MAH or D-MAH) and prepare the application. ■ Submit the application for medical device certification. ■ Conduct QMS conformity assessment. *For more details, please refer to the PDF materials or feel free to contact us.

  • Other contract services
  • others

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[Information] Environmental Management System ISO 14001

[Information] Environmental Management System ISO 14001

Improving the workplace environment to boost employee motivation! Introduction of benefits and more.

As environmental destruction due to corporate activities progresses, the depletion of resources is beginning to be recognized as a real issue. To break this situation, the first edition of ISO 14001 was issued in 1996. Environmental protection is becoming an increasingly important role for all organizations, and environmental management system standards are becoming a crucial prerequisite for succeeding in the global market. Regarding environmental performance, we recommend activities that are appropriate for the corporate level, taking into account factors such as corporate value (corporate image) and collaboration with the community. [Benefits of Acquisition (Excerpt)] ■ Improvement of reliability in environmental management ■ Reduction of risks of environmental accidents and disasters in the workplace ■ Increased motivation of employees due to improvements in the workplace environment ■ Enhanced business performance due to improvements in the workplace environment ■ Improvement of corporate image by demonstrating the company's commitment to environmental management to the public and related companies *For more details, please refer to the PDF document or feel free to contact us.

  • ISO certification body

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