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

76～83 item / All 83 items

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DQS Japan【MDR Latest Information】Conditions for Extension of MDD Transition Period

DQS Japan【MDR Latest Information】Conditions for Extension of MDD Transition Period

We will deliver the latest information on MDR. This time's theme is "What are the conditions for the extension of the MDD transition period?"

On March 15, 2023, the European Council passed a proposal by a majority vote to extend the validity period for high-risk devices already certified under the MDD until May 2027, and for medium-risk and low-risk devices until May 2028. The official announcement was published in the EU Official Journal on March 20, 2023. The extension of the deadline is conditional upon companies that have obtained current MDD certification completing their formal MDR applications to the Notified Body (N.B.) by May 26, 2024, and finalizing contracts as stipulated in MDR Annex VII section 4.3 with the N.B. by September 26, 2024. Only legacy devices under the MDD (MDCG 2021 25), meaning devices that were placed on the market after the application date of the MDR (May 26, 2021), are eligible to apply for the extension. DQS is still accepting new MDR applications, but this decision is expected to prompt a rush of applications for the 70% of MDD-certified products that have not yet applied for MDR by 2024. Additionally, even for products already certified under the MDD, obtaining MDR certification will be necessary for design changes, so the resource shortage at the N.B. during the transition period is likely to continue.

  • Quality assurance support systems and services

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[JinCreek Case Study] Government Agencies

[JinCreek Case Study] Government Agencies

A case where existing PCs are used to reduce costs and prevent misuse even in the event of loss!

We would like to introduce a case where our product "JinCreek" was implemented in a government agency. Due to challenges such as "wanting to conduct business without connecting to the internet" and "wanting to utilize computers that do not support SIM cards," we proposed the urgent establishment of a telework environment. After implementation, it became possible to combine external communication devices, allowing for the realization of this without purchasing new computers. Additionally, external communication devices could also serve as authentication elements, resulting in a level of security that exceeded expectations. [Challenges] ■ Wanting to conduct business without connecting to the internet ■ Wanting to utilize existing computers (traditional PCs that do not support SIM cards) *For more details, please refer to the PDF document or feel free to contact us.

  • Other security

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[JinCreek Case Study] Medical Device Manufacturer

[JinCreek Case Study] Medical Device Manufacturer

There are many tasks after returning to the office from external duties! A case study on how the frequency of returning to the office has decreased and efficiency has improved.

We would like to introduce a case where our product 'JinCreek' was implemented for a medical device manufacturer. Previously, there were challenges such as the difficulty of coordinating the schedules of accompanying personnel during meetings at client sites, and a lack of information regarding security in telework, making it hard to make decisions. After implementation, employees can conduct business online anytime by simply opening their computers, and it has become easier to coordinate schedules as accompanying personnel can now participate in meetings via web conferencing. [Challenges] ■ There are many tasks to handle after returning from fieldwork, and we want to reduce the burden on employees. ■ It is difficult to coordinate the schedules of accompanying personnel during meetings at client sites. ■ There is little information on security in telework, making it hard to make decisions. *For more details, please refer to the PDF document or feel free to contact us.

  • Other security

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[Research Material] The Global Market for Testing, Inspection, and Certification

[Research Material] The Global Market for Testing, Inspection, and Certification

Global Market for Testing, Inspection, and Certification: In-house, Outsourced, Consumer Goods, Products, Industrial, LFE, Others

This research report (Global Testing, Inspection and Certification Market) investigates and analyzes the current state and outlook for the global testing, inspection, and certification market over the next five years. It includes information on the overview of the global testing, inspection, and certification market, trends of major companies (sales, selling prices, market share), market size by segment, market size by major regions, and distribution channel analysis. The segments by type in the testing, inspection, and certification market focus on in-house and outsourcing, while the segments by application target consumer goods, products, industrial, LFE, and others. The regional segments are categorized into North America, the United States, Europe, Asia-Pacific, Japan, China, India, South Korea, Southeast Asia, South America, the Middle East, and Africa, to calculate the market size for testing, inspection, and certification. It also includes the market share of major companies in testing, inspection, and certification, product and business overviews, and sales performance.

  • Other services

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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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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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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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