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 30 Manufacturers, Suppliers and Companies

Last Updated： Aggregation Period:Aug 20, 2025～Sep 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:Aug 20, 2025～Sep 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. SGSジャパン Kanagawa//Service Industry
  4. 4 DEKRAサーティフィケーション・ジャパン Tokyo//others 医療機器事業部
  5. 5 一般財団法人日本品質保証機構 Tokyo//Testing, Analysis and Measurement 計量計測部門、総合製品安全部門
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Authentication Services Product ranking

Last Updated： Aggregation Period:Aug 20, 2025～Sep 16, 2025
This ranking is based on the number of page views on our site.

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

Authentication Services Product List

46～60 item / All 78 items

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Medical Device CE Mark Certification Service

Medical Device CE Mark Certification Service

Leave the "CE" mark certification for medical devices for the European market to us!

We provide "CE mark" certification services that declare compliance with all safety, health, and environmental protection requirements specified in the Medical Device Directive. The CE certificate is valid for three years from the date of issuance, after which renewal of the certificate is required. Please feel free to contact us if you have any requests. 【Process to Obtain Certification】 1. Document Review 2. On-site 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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From application to certification in as little as 3 months! ISMS examination and certification service.

From application to certification in as little as 3 months! ISMS examination and certification service.

Minimal impact on daily operations with no chaos before the audit. Obtain ISMS in as little as 3 months! We resolve concerns such as not knowing what to do before the audit.

We offer a flexible "ISMS Audit and Certification Service" that can accommodate schedule adjustments. Online meetings and estimates are available, and we can also conduct remote audits. Audits that typically take two days with standard certification bodies can sometimes be completed in one day, allowing for flexible scheduling of the audit dates. Primarily, you can undergo the audit by explaining your daily business activities. Please feel free to consult us when you need our services. 【Features】 ■ Fastest certification from application in 3 months ■ Minimal impact on daily operations ■ Audits tailored to your business activities ■ No last-minute rush before the audit ■ Support for remote audits *For more details, please refer to the PDF materials or feel free to contact us.

  • Management Seminar

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[Blog] Strengthening Security by Increasing the Bit Count of DKIM Keys

[Blog] Strengthening Security by Increasing the Bit Count of DKIM Keys

Together with SPF and DMARC, we have dramatically improved the email security systems of organizations around the world.

Due to the threats lurking on the internet, companies need to adopt strong authentication methods to prove their legitimacy. One common method is DKIM (DomainKeys Identified Mail). This is an email authentication technology that uses cryptographic keys to verify the sender's domain, and using DKIM confirms the sender's domain. In this article, we will introduce how to upgrade the DKIM key for Microsoft Office 365 Exchange Online from 1024 bits to 2048 bits. [Contents] ■ The importance of upgrading the length of DKIM keys ■ Manually upgrading DKIM keys using Exchange Online PowerShell *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 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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MDSAP (Medical Device Single Audit Program for Canada, the United States, Brazil, and Australia)

MDSAP (Medical Device Single Audit Program for Canada, the United States, Brazil, and Australia)

To those considering entering the medical device market (Canada, the United States, Brazil, Australia)

To those considering entering the medical device market (Canada, the United States, Brazil, Australia): Introducing MDSAP certification.

  • Other quality control and hygiene measures

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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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ISO/IEC 27001: 2022 Edition Revision Commentary

ISO/IEC 27001: 2022 Edition Revision Commentary

[Online Seminar] Duration is 3 hours. We support everyone who wants to gather information early and prepare in advance!

This seminar supports those who want to gather information early and prepare in advance for the upcoming revised edition of ISO/IEC 27001, which will be published soon. The duration is 3 hours, and the content is summarized compactly. We sincerely look forward to your participation. 【Overview】 ■Location: Online ■Language: Japanese ■Capacity: 50 participants (registration will close once the capacity is reached) ■Date: Ongoing from April 2023 *Please feel free to contact us.

  • Management Seminar

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[Blog] What is documented information?

[Blog] What is documented information?

Is a quality management manual really essential? Introducing it on the blog.

In previous versions of international standards for management systems, terms such as "documents," "documented requirements," "documents," and "records" were still used. Currently, ISO standards consolidate these terms under "documented information." However, the use of this collective term is not mandatory for users of the standards. Of course, those who wish can continue to use their company's unique terminology when dealing with documented information. 【Contents】 ■ How is documented information defined? ■ Is any documented information considered "documented information"? ■ How do you create documented information? ■ To what extent must it be created? ■ Is a quality management manual still essential? ■ Conclusion: Documented information *Our company also conducts seminars related to relevant standards from time to time. For more details, please download the PDF or feel free to contact us.

  • ISO certification body

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