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
Go to Company Ranking

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

61～75 item / All 88 items

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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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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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[Blog] Three Strengths of Quality Management Adapted to Digitalization

[Blog] Three Strengths of Quality Management Adapted to Digitalization

How will QM be affected during this transformation process? This will be introduced in the blog.

To continue being a strong partner in production and services, how should quality management (QM) confront the changes brought about by digitalization? The Senior Quality Manager of Siemens AG's Digital Industries division focused on two questions at the DQS Customer Day event held in Karlsruhe. What impact will QM experience during this transformation process? And what contributions can QM make towards digitalization? 【Contents】 ■ Quality Management: A Reliable Response to Digitalization ■ Digital Transformation: Recognizing Future Changes ■ Great Opportunity: Quality Managers Must Be Role Models ■ Quality Managers Lead *We also hold seminars on related 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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[Blog] Current Standards for TISAX Assessment

[Blog] Current Standards for TISAX Assessment

Main changes from VDA ISA 5.0 - Introduction to the blog article!

Since 2022, the new VDA ISA Catalog 5.1 has been applied to all new TISAX assessments. According to VDA, there have been only minor changes from version 5.0. The new TISAX 5.1 test catalog has been further simplified and enables more efficient work for both users and testers. [Contents] ■ Main changes in VDA ISA 5.1 ■ What is the deadline for users? ■ TISAX 5.1 - Background information ■ DQS - A suitable partner from the start *We also hold seminars on related 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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【Blog】What is IATF?

【Blog】What is IATF?

Improve the overall quality of products in the automotive industry! Mission of the International Automotive Task Force.

The task force, established in 1996, currently represents major automotive manufacturers (OEMs) in the United States, India, and Europe (Germany, France, the United Kingdom, Italy) as well as supplier associations from various countries. However, not all international automotive manufacturers are members of the IATF, particularly in Southeast Asia (such as Japan, South Korea, and China). The mission of the IATF is to harmonize the quality management methods and quality management standards implemented in each country, thereby improving the overall quality of products in the automotive industry. *Our company also conducts seminars on related 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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Multi-Factor Authentication Service "JinCreek"

Multi-Factor Authentication Service "JinCreek"

We will achieve the highest level of security in telework and promote digital transformation (DX).

"JinCreek" is an authentication service that prevents impersonation and unauthorized access through authentication with three or more elements, serving as an alternative to ID/PASS and accommodating various network configurations. By eliminating the concept of external access and allowing access within the company's IP address range, it is possible to maintain a state as if one is present in the office even when outside the company. Additionally, biometric authentication can be freely chosen, allowing for optimization of which authentication elements are most suitable for the company while enhancing security. [Reasons for Choosing Us] ■ Identity verification through multi-factor authentication ■ Compatibility with various network configurations ■ Enables AD integration and continuity of policies ■ Enhanced security through variable elements ■ Possible integration with existing carriers and current authentication systems ■ Integration with software is also possible *For more details, please download the PDF or feel free to contact us.

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

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iPad Compatible: Make Telecommuting Safer with Stronger Security!

iPad Compatible: Make Telecommuting Safer with Stronger Security!

Achieve the same access environment as the office even during telework, balancing enhanced security and improved operational efficiency!

In recent years, the spread of remote work has led to an expansion in the use of devices such as iPads for business purposes in general companies, local governments, and educational institutions. However, with the traditional security level, once the device is unlocked, there is no authentication of the device or the user, allowing unlimited access to the SIM closed network. In the event that the device or SIM is lost or stolen, there is a risk that malicious third parties could use the device to infiltrate the customer's business network and gain unauthorized access, which is one of the challenges. This service, "JinCreek for Quick Access," addresses the user's challenge of "improving information security during remote access." It is also possible to enhance security tailored to the user's operations. For more details, please download the materials or contact us.

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

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[Model Case] Construction and Manufacturing

[Model Case] Construction and Manufacturing

Providing a system that enables remote implementation with enhanced security guarantees!

We would like to introduce examples of utilizing our 'JinCreek' in industries such as construction and manufacturing. We provide a system that enables remote collaboration between the field and management, as well as the sharing of information and operations from headquarters, all while ensuring security and safety. Additionally, we conduct multi-factor personal authentication through a simple system via closed networks or Internet VPNs, balancing efficiency and safety. 【Business Challenges and Effects】 ■ Measures to prevent the leakage of important blueprints and similar documents are crucial, necessitating a system to identify individuals using devices such as computers to prevent unauthorized use. ■ The exchange of data between construction/manufacturing sites and management/headquarters has increased the number of tools, making both work and data heavier, but we want to achieve a more secure environment more easily. ■ In some locations, it is difficult to establish communication environments like Wi-Fi, and we want to enable remote work using LTE (SIM closed network) that allows for safe and reliable communication. *For more details, please refer to the PDF document or feel free to contact us.

  • Other security

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[Model Case] Medical Care

[Model Case] Medical Care

Block unauthorized access to and use of information to enhance safety!

We would like to introduce examples of how our service "JinCreek" can be utilized in industries such as healthcare. In medical institutions that handle sensitive and highly confidential personal information, we block unauthorized access and use of information to enhance safety. Additionally, while ensuring the security of medical information, we enable medical institutions to establish a telework environment safely and swiftly, thereby improving operational efficiency. 【Business Challenges and Effects】 ■ As infectious diseases spread, the handling of electronic medical records and medical information is a highly confidential task, leading to delays in the adoption of telework and increased workload. ■ There are also significant challenges in identifying doctors and staff within the network, necessitating a system that allows for easy personal authentication while maintaining high security. *For more details, please refer to the PDF document or feel free to contact us.

  • Other security

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[JinCreek Case Study] B Local Government in Chiba Prefecture

[JinCreek Case Study] B Local Government in Chiba Prefecture

Introducing examples that ensure employee safety and time reduction, which can also be applied to remote work!

We would like to introduce a case study of the implementation of "JinCreek" in a local government in Chiba Prefecture. Previously, after taking photos with a digital camera, there was a time lag and burden on staff as they had to return to the office to upload images of the disaster area, no matter how late it was. After the implementation, remote data uploads from the field became possible, ensuring the safety of staff and reducing time. [Case Overview] ■ Issues - There was a time lag and burden on staff as they had to return to the office to upload images of the disaster area after taking photos. - We wanted to connect to the business network without using the internet. ■ Implementation Effects - Remote data uploads from the field became possible, ensuring the safety of staff and reducing time. - Since it is a SIM closed network connection, it became possible to connect to the business network. *For more details, please refer to the PDF document or feel free to contact us.

  • Other security

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