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Validation Product List and Ranking from 6 Manufacturers, Suppliers and Companies

Last Updated： Aggregation Period:Sep 17, 2025～Oct 14, 2025
This ranking is based on the number of page views on our site.

Validation Manufacturer, Suppliers and Company Rankings

Last Updated： Aggregation Period:Sep 17, 2025～Oct 14, 2025
This ranking is based on the number of page views on our site.

  1. セントラル科学 Tokyo//Trading company/Wholesale
  2. ステリテック Saitama//others
  3. AndTech Kanagawa//Service Industry
  4. 4 ダイキンアプライドシステムズ Tokyo//Industrial Machinery
  5. 5 null/null
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Validation Product ranking

Last Updated： Aggregation Period:Sep 17, 2025～Oct 14, 2025
This ranking is based on the number of page views on our site.

  1. Cleaning validation using the Sievers TOC meter. セントラル科学
  2. Validation of the TOC method for cleaning validation. セントラル科学
  3. About sterilization validation ステリテック
  4. 4 Points on planning and implementing experimental design for analytical method validation, and considerations for the procedure. AndTech
  5. 5 TOC-based lab/at-line/online cleaning validation セントラル科学

Validation Product List

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Online cleaning validation using TOC, IC, and conductivity.

Online cleaning validation using TOC, IC, and conductivity.

Application Note: Optimization of Cleaning Conditions Using an Online TOC Analyzer

Cleaning validation is an essential process in pharmaceutical manufacturing. However, traditional manual sampling and swab testing are time-consuming, carry a high risk of human error, and are costly. This is where Process Analytical Technology (PAT) comes into play. Based on guidance published by the FDA in 2004, this technology provides recommendations for understanding, controlling, and continuously verifying processes. By using PAT, it becomes possible to understand processes without manual sampling or analysis, leveraging real-time data. Utilizing real-time data on TOC, IC, and conductivity from online TOC analyzers enables comprehensive understanding of the cleaning process through online cleaning validation.

  • アットラインCV_M9P.jpg
  • アットラインCV_CIPからの排水.jpg
  • Analytical Equipment and Devices

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Validation

Validation

Achieved validation of quality risk management implemented in collaboration with our customers!

We would like to introduce the "validation" that we conduct. In Japan, the introduction of "quality risk management" and "evaluation throughout the lifecycle necessary for continuous improvement" are essential. We share new validation information and work together with our customers to carry out validation and support the completion of projects. 【Flow of Validation Implementation (Partial)】 ■ Design Qualification ■ Master Plan ■ Installation Qualification ■ Calibration ■ Operational Qualification *For more details, please refer to the related links or feel free to contact us.

  • Contract Inspection

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【資料】放射線滅菌バリデーション

【資料】放射線滅菌バリデーション

製品性能の適格性や稼働性能適格性、滅菌線量の監査等を各種掲載しています

当資料では『放射線滅菌バリデーション』についてご紹介しています。 「放射線滅菌バリデーション実施項目」をはじめ「照射容器内線量分布」や、 「滅菌線量設定方法の概要」について、図や表を用いて全2ページで詳しく 掲載。 技術委託の参考資料としてご活用ください。 【掲載内容】 ■放射線滅菌バリデーション実施項目一覧 ■照射容器内線量分布 ■滅菌線量　設定方法の概要 ※詳しくはPDF資料をご覧いただくか、お気軽にお問い合わせください。

  • Other contract services

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Validation related to clean rooms and clean equipment.

Validation related to clean rooms and clean equipment.

Leave the validation of clean rooms and clean equipment to us.

We will inspect whether clean rooms, clean equipment, and experimental instruments are operating properly using various measuring devices. After the inspection, we will prepare a report and, if necessary, propose repairs or maintenance for the equipment. 【Service Contents】 - Measurement work for clean rooms (ICR, BCR) - HEPA filter replacement - Measurement of airborne and settled bacteria - Inspection and measurement of various clean room equipment - Inspection and maintenance of local exhaust systems (e.g., draft chambers) - Inspection and maintenance of clean benches - Inspection and maintenance of nanomaterial cabinets - Inspection and maintenance of biohazard cabinets - Inspection and maintenance of scrubbers - Inspection and maintenance of chemical hazard cabinets - Inspection and maintenance of glove boxes

  • 手術室3　清浄度測定 (2).jpg
  • DSCF3538.jpg
  • others

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About sterilization validation

About sterilization validation

Our company also conducts sterilization validation services, various bacterial tests, and residual gas analysis.

At Steritech Co., Ltd., we conduct sterilization validation services. We perform pre-conditioning to adjust temperature and humidity to ensure that products are in a state that is easy to sterilize, and we also remove air from the products by applying vacuum and introducing EOG, among various other processes. Please feel free to contact us when you need our services. 【Examples of Sterilization Processes】 ■ Pre-conditioning ■ Vacuum ■ Humidification ■ EOG Introduction ■ Action Time ■ Air Replacement *For more details, please refer to the PDF materials or feel free to contact us.

  • Other contract services

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Cleaning validation using the Sievers TOC meter.

Cleaning validation using the Sievers TOC meter.

The use of TOC in cleaning validation is gaining attention.

TOC is an effective tool for cleaning validation of pharmaceuticals, cosmetics, and medical devices. By using TOC for cleaning validation, improvements in quality, risk reduction, and efficient operations can be achieved. TOC is a simple analytical method that rapidly detects low concentrations of organic compounds and can identify degradation products and contaminants that HPLC cannot detect. Compared to HPLC, which is a specific analytical method that detects only specific components, TOC, being a non-specific analytical method, can comprehensively confirm that excipients, degradation products, and cleaning agents are adequately cleaned. Furthermore, TOC simplifies method development and minimizes equipment downtime, leading to increased efficiency. By using TOC, not only can the cleaning process be evaluated quickly, but it also reduces the workload, maintenance costs, and running costs compared to HPLC.

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  • CIP.png
  • Other physicochemical equipment

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Validation of the TOC method for cleaning validation.

Validation of the TOC method for cleaning validation.

[Application Note] Introducing the validation of analytical methods for TOC in cleaning validation.

The TOC method for cleaning validation is an important technique for evaluating the cleanliness of equipment. The TOC method is recognized as a way to assess the carbon content in samples and is used to evaluate the cleanliness of equipment. In accordance with ICH Q2B guidance, examples of the evaluation of various parameters related to the validation of analytical methods using TOC will be introduced.

  • CIP.png
  • Analytical Equipment and Devices

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TOC-based lab/at-line/online cleaning validation

TOC-based lab/at-line/online cleaning validation

The Sievers TOC meter for cleaning validation is effective in various situations such as lab, at-line, and online, depending on the application.

TOC and conductivity are important analytical items that support cleaning validation, cleaning verification, and cleaning monitoring. TOC measurements can be performed in response to user requests in various settings, including laboratories, manufacturing sites (at-line), and online (final rinse water monitoring from CIP).

  • アットラインCV_M9P.jpg
  • オンラインCV.jpg
  • スワブ操作.png
  • Analytical Equipment and Devices

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Points on planning and implementing experimental design for analytical method validation, and considerations for the procedure.

Points on planning and implementing experimental design for analytical method validation, and considerations for the procedure.

Points on planning and implementing experimental design for analytical method validation and examination procedures.

1. Purpose of Analytical Method Validation 2. Experimental Design for Analytical Method Validation 3. Implementation Methods for Analytical Method Validation 4. Key Points for Examining Linearity 5. Key Points for Examining DL/QL 6. Key Points for Examining Accuracy 7. Methods and Evaluation of Precision Calculation 8. General Precautions 9. Comparison of Old and New Quantitative Methods for AAA Preparations 10. Points to Note in Stability Testing 11. System Suitability in HPLC Methods 12. Considerations for Setting Standards 13. Quality Standards for Investigational Drugs 14. Technology Transfer 15. Outsourcing to External Testing Organizations 16. Quality System (ICH Q10) and Quality Risk Management (ICH Q9) 17. Risk Management & Compliance [Q&A and Business Card Exchange] *Requests for content in advance are also welcome!*

  • Chemicals
  • Technical Seminar
  • others

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