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Management System Product List and Ranking from 40 Manufacturers, Suppliers and Companies

Last Updated： Aggregation Period:Sep 03, 2025～Sep 30, 2025
This ranking is based on the number of page views on our site.

Management System Manufacturer, Suppliers and Company Rankings

Last Updated： Aggregation Period:Sep 03, 2025～Sep 30, 2025
This ranking is based on the number of page views on our site.

  1. null/null
  2. 東計電算 製造システム営業部 (第一事業所) Kanagawa//IT/Telecommunications
  3. ネクスタ Osaka//software
  4. 4 日鉄テックスエンジ システムソリューション事業部 Tokyo//others
  5. 5 株式会社ハイブリッチ／ビス Tokyo//IT/Telecommunications
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Management System Product ranking

Last Updated： Aggregation Period:Sep 03, 2025～Sep 30, 2025
This ranking is based on the number of page views on our site.

  1. Explanatory Material "Basic Knowledge of Production Management Systems" *Currently available for free.
  2. GxP Quality Document 10: How to Properly Manage Blank Forms
  3. Equipment Maintenance Management System "UNIVEAM4" new 日鉄テックスエンジ システムソリューション事業部
  4. 4 QUALISCAN QMS-12 Traverse-type Quality Management System 東洋機械
  5. 5 DX of Calibration Management: Manage Measuring Instruments Collectively! Measuring Instrument Calibration Management System 日本メカトロン 大阪事業所

Management System Product List

5251～5265 item / All 5378 items

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Achieving DX! "Cloud-based Production Management System for Sheet Metal"

Achieving DX! "Cloud-based Production Management System for Sheet Metal"

Ideal for eliminating dependency on specific individuals in business operations! Centralized data management with easy operation! Can be implemented at a low cost! *Case studies available.

"Taktory" is a cloud-based production management system for sheet metal that does not require server installation or network setup, utilizing a web system. Data is backed up in the cloud, allowing all employees to share work lists, load statuses, and more. Additionally, data created using our developed sheet metal CAD/CAM software "CADMAC(R)-NEX" is automatically registered in the product master of this system via the cloud server. We provide case studies of companies that have implemented a production management system for the first time, as well as those that have replaced their existing systems. 【Features】 ■ A flat rate for up to 50 users per account ■ Accessible from any device connected to the internet ■ All data is managed in the cloud, allowing access from anywhere, both inside and outside the company ■ iOS app allows for camera use, making it easy to register photos and scan barcodes ■ CADMAC(R)-NEX integration features (product registration and nesting integration) ■ Capable of integration with core systems and accounting systems *For more details, please download the PDF or feel free to contact us.

  • Production Management System

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Introduction of case studies from manufacturers.

Introduction of case studies from manufacturers.

Introduction of effects: Project value capture +5%, capital efficiency +2%, etc., examples from manufacturing companies.

Information distributed across multiple systems, extensive manual reporting and analysis... Delays in portfolio management and investment decisions due to increasing complexity. We present case studies of global companies that have eliminated such inefficiencies and ensured visibility across the organization through centralized management.

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  • project management

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Cloud-based document management system "Agatha Basic"

Cloud-based document management system "Agatha Basic"

For companies looking to achieve paperless solutions in line with Part 11 compliance! We enable a small start in both cost and scale.

Agatha Basic is a document management cloud service equipped with basic functions for sharing, storing, and managing documents related to clinical trials and research. It is a high-security, highly reliable system compliant with ER/ES guidelines, FDA regulations, and CFR 21 Part 11. It is simple and easy to use, and during implementation, dedicated consultants provide support, along with ongoing assistance from a help center, ensuring that even first-time users can use the document management system with confidence. <Recommended for> ● Those who are managing documents on paper and want to reduce the enormous workload and costs involved. ● Those who want to manage and share documents in compliance with ER/ES and CFR Part 11. ● Those who wish to achieve seamless information sharing and management beyond location and time constraints, whether on the go or across multiple facilities. ● Those who find file management complicated due to not knowing the latest version or accidentally overwriting files. ● Those troubled by the rising costs, complexity, and operation of existing systems. ● Those considering the latest security measures and disaster/pandemic response (BCP/BCM). *For more details, please refer to the PDF materials or feel free to contact us.

  • Document and Data Management

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[On-Demand Webinar] Data Integrity Compliance Seminar

[On-Demand Webinar] Data Integrity Compliance Seminar

Mr. Murayama from eCompliance Co., Ltd. will be speaking! Seminar on Data Integrity in relation to deviations, CAPA, change management, etc.

You can watch the video of the webinar held on May 17, 2024. Seminar on Data Integrity in Deviation, CAPA, and Change Management ~ Event management to comply with regulatory requirements in Japan, the U.S., and Europe ~ As data integrity measures progress, the pharmaceutical and medical device industries are required to manage a multitude of event data, including deviation management, change management, CAPA, nonconformance management, training, and audits. There are limitations to managing data based on human input, such as with Word and Excel, and we often hear about situations where related documents are stored separately due to paper management, making it impossible to manage them in a linked manner. Event data should inherently be interconnected, and it is crucial to have quick access to related data. So, how can we effectively manage these often complex data sets? In this seminar, we will clearly explain the principles of event management and how to ensure data integrity.

  • others

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Clinical Trial Document Management System_Case Study at the Japan Complement Society

Clinical Trial Document Management System_Case Study at the Japan Complement Society

Introducing a case study on streamlining document sharing and management in clinical research!

We would like to introduce a case study of the implementation of "Agatha Basic" by the Japan Complement Society. The society was previously exchanging test data and case reports via email, but this method was very cumbersome, required the hassle of password protection, and posed a risk of misdelivery. After the implementation, it became possible to simply enter progress into Excel and save it, allowing stakeholders to constantly share new information and retrieve past information when needed. 【Key Factors for Implementation】 ■ Usable on MAC ■ Easy to read and use ■ Easy to start *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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Clinical Trial Document Management System_Example at Mediscience Planning Co., Ltd.

Clinical Trial Document Management System_Example at Mediscience Planning Co., Ltd.

Introducing a case study of implementing eTMF in CRO at a low cost!

We would like to introduce a case study of the implementation of "Agatha eTMF" by Mediscience Planning Co., Ltd., a company with a rich history in the CRO industry. The company has started to consider the implementation of eTMF due to an increasing number of requests from global clients wanting to utilize it. After the implementation, Agatha is being used not only as a tool to manage essential documents for the clinical trials they undertake but also to manage internal SOPs, thereby expanding its use as their document management platform. 【Benefits of Implementation】 ■ The greatest advantage is ease of use ■ Flexible clinical trial document list ■ Compliance with high security requirements in the healthcare and life sciences fields ■ Risk-based Monitoring (RBM) *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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Clinical Trial Document Management System: A Case Study at Tohoku University Hospital Clinical Trial Data Center

Clinical Trial Document Management System: A Case Study at Tohoku University Hospital Clinical Trial Data Center

A case of enhancing document management in clinical research through tamper prevention and version control!

We would like to introduce a case study on the implementation of "Agatha Basic" by the Tohoku University Hospital Clinical Trial Data Center, which supports data management for clinical research conducted by Tohoku University. At this center, managing documents on a file server involved significant operational burdens, such as strictly adhering to file naming and storage rules, and converting important documents into paper versions. After the implementation, we received feedback that document sharing could be done smoothly without being constrained by location. 【Case Overview】 ■ How Agatha is Used - Management of QMS documents and SOPs at the data center - Management of research project documents ■ Benefits of Implementation - Utilized system functions such as version control, tamper prevention, and approval records in operations - Became able to recognize and manage the benefits and risks of document management and systems *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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Case study of clinical trial document management system in Mablink Bioscience.

Case study of clinical trial document management system in Mablink Bioscience.

Achieve compliance with Agatha! Quality guaranteed, required both medically and in management.

We would like to introduce a case study on the implementation of "Agatha QMS" by Mablink Bioscience, a biotechnology company based in France. The company wanted to manage clinical trials from the beginning with the appropriate methods, processes, and systems. By using Agatha, they can obtain the necessary data from documents and forms, allowing them to smoothly advance through each stage of the trial. [Case Overview] ■Challenges - There was no way to register and manage documents for each trial phase. - It was difficult to find files. ■Benefits - All trial-related documents and administrative paperwork can be easily managed. - They can grant access to VCs for information provision during fundraising. *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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Clinical Trial Document Management System_CRO (Contract Research Organization) Case Study

Clinical Trial Document Management System_CRO (Contract Research Organization) Case Study

Agatha enhances its services as a CRO with eTMF! Improving daily TMF management.

We would like to introduce a case study on the implementation of "Agatha eTMF" at DZS Clinical Services, a full-service CRO. The company faced challenges related to document quality management and collaboration among various stakeholders, including facilities, sponsors, different personnel, and management. After the implementation, we received feedback that the initiation of trials, registration of facilities and users, and document registration have become significantly more efficient than before. 【Case Overview】 ■Challenges - Managing the process of quality checks for clinical trial-related documents - Verifying that all necessary documents are complete ■Benefits - Document naming and management are consistent with standard methods, making it user-friendly for CRAs - Quality management of documents can be conducted within the system, allowing for easy report generation *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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Clinical Trial Document Management System_Case Study in a Biopharmaceutical Company

Clinical Trial Document Management System_Case Study in a Biopharmaceutical Company

Agatha achieves in-house production with eTMF! The system can be configured according to operational methods.

We would like to introduce a case study of "Agatha eTMF" by InCarda Therapeutics, which conducts clinical development in California, USA. The company had outsourced TMF management, but it became increasingly complicated, and it was clear that a more rational and cost-effective operational method was needed. The implementation project was completed in about six weeks and included various configuration changes, document classification definitions, the addition of new fields such as responsible persons and affiliations through an automatic naming function, and user training. [Case Overview] ■ Challenges - Difficulty in document verification, requiring manual tracking for quality checks - Need to directly check TMF documents whenever an issue arose ■ Benefits - Ability to configure the system according to operational methods - Automatic verification of all documents within the system without relying on manual processes *For more details, please download the PDF or feel free to contact us.

  • Document and Data Management

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