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  6. EP Revision Response: Explanation of New Standards for TOC Testing and Reference Values by Container Volume

EP Revision Response: Explanation of New Standards for TOC Testing and Reference Values by Container Volume

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Sievers

last updated:Oct 09, 2026

セントラル科学
セントラル科学
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Are you ready to prepare for the revision of EP 12.3? A clear explanation of the new requirements for TOC testing and the standard values by container capacity.

The European Pharmacopoeia (EP) 12.3 edition, which came into effect on July 1, 2026, has significantly revised the requirements for TOC testing of pharmaceutical water. It includes mandatory use of EP CRS reference standards and the introduction of TOC criteria based on container capacity for sterilized water for injection, which will have a major impact on quality control operations in the pharmaceutical industry. This document summarizes the key points of the revisions and explains the impact on equipment performance and operations during the transition to EP reference standards.

    Other water quality analysisWater quality testingPharmaceutical water production equipment and facilities
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EP Revision Response: Explanation of New Standards for TOC Testing and Reference Values by Container Volume

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SST.jpg
  • Related Link - https://aqua-ckc.jp/topic/epstandard
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【What can be understood from this document】 - Main revisions of the TOC test in EP version 12.3 - Requirements for EP CRS reference standards in system suitability testing - New TOC reference values set by container volume (Method B) - Transition points for TOC testing in sterilized water for injection - Comparative evaluation results of EP reference standards and USP reference standards using Sievers TOC analyzers - Corresponding methods for validated TOC analyzers and new TOC analyzers - Necessity of firmware updates, recalibration, and equipment modifications

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【Recommended for the following customers】 - Quality control (QC) personnel at pharmaceutical companies - Personnel responsible for the operation and management of pharmaceutical water systems - Personnel involved in GMP, CSV, and validation - Companies that manufacture and export products for the European Pharmacopoeia (EP) - Those considering updates to TOC analyzers or regulatory compliance

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Revision of EP regulations: New standards for TOC testing and new standard values by container capacity.

Revision of EP regulations: New standards for TOC testing and new standard values by container capacity.

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Standard solution for TOC measurement

Standard solution for TOC measurement

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Pharmaceutical Water _ TOC Meter for Cleaning Validation Sievers M9

Pharmaceutical Water _ TOC Meter for Cleaning Validation Sievers M9

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TOC Analyzer for Pharmaceuticals Sievers M9

TOC Analyzer for Pharmaceuticals Sievers M9

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Online TOC Analyzer Sievers M500

Online TOC Analyzer Sievers M500

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Sievers TOC Sensor CheckPoint Pharma

Sievers TOC Sensor CheckPoint Pharma

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Sievers standard solution contamination management strategy

Sievers standard solution contamination management strategy

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Traceability of Sievers standard solution and vials

Traceability of Sievers standard solution and vials

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Are you ready for the system suitability testing of the TOC analyzer compliant with the European Pharmacopoeia (EP 12.3) revision?

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The revision of the EP that came into effect on July 1, 2026, has significantly changed the requirements for the system suitability test (SST) of TOC analyzers. After the implementation of EP 12.3, in order to clarify standardization and traceability within the EP, the standard solutions for the system suitability test of TOC analyzers must use sucrose and 1,4-benzoquinone, which are certified as EP reference substances (Chemical Reference Substances: CRS). With the EP standard solution becoming the new standard, if USP standard solutions are to be continued, it is necessary to explain the validity of adopting USP reference substances. We have published a page on our website that explains the key points of the revision, necessary responses, considerations for continuing to use USP standard solutions, and ways to utilize EP standard solutions to reduce operational burdens. If you are considering how to respond to the EP revision, please take a look at the related links. Additionally, in the related materials, we provide detailed information on the requirements for standard solutions, reference values by container type, and comparative evaluation results using Sievers TOC analyzers, highlighting key points for quality control and regulatory compliance of pharmaceutical water.

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セントラル科学

セントラル科学

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Since our establishment in 1967, we have been dedicated to the development and dissemination of water quality measurement devices that anyone can use quickly, easily, and with high precision. In today's world, where the effective use of water, a limited resource, is required alongside environmental conservation, we aim to be a total solution provider that responds to all water environments by utilizing our water quality measurement devices, technology, and services. Furthermore, leveraging the latest technology and years of know-how, we are committed to delivering user-friendly and reliable water quality measurement devices more affordably, quickly, and widely.

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