ASTM International Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment ASTM E3466-25

Description
1.1 In this guide, guidance on the development of particle quantification test methods that determine the count and sizes of particulate matter present on the surfaces of single-use bioprocessing equipment (single-use systems (SUS)) applied in biopharmaceutical manufacturing processes is described. 1.2 In particle quantification test methods, liquid is applied to extract particulate matter from the surfaces of SUS, and the extract is subsequently analyzed with a particle measurement technique to determine particle count and sizes. 1.3 This guide is limited to the application of the particle measurement techniques described in the pharmacopoeia for parenteral drug products: light obscuration (LO), membrane microscopy (MM), and flow imaging (FI). 1.4 In this guide, the commonly applied size classifications for subvisible (10?μm to 100?μm) and visible (=100?μm) particulate matter are adopted. 1.5 For the validation requirements for particle quantification test methods, see Practice E3468. 1.6 Units\u2014The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard. 1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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Description
1.1 In this guide, guidance on the development of particle quantification test methods that determine the count and sizes of particulate matter present on the surfaces of single-use bioprocessing equipment (single-use systems (SUS)) applied in biopharmaceutical manufacturing processes is described. 1.2 In particle quantification test methods, liquid is applied to extract particulate matter from the surfaces of SUS, and the extract is subsequently analyzed with a particle measurement technique to determine particle count and sizes. 1.3 This guide is limited to the application of the particle measurement techniques described in the pharmacopoeia for parenteral drug products: light obscuration (LO), membrane microscopy (MM), and flow imaging (FI). 1.4 In this guide, the commonly applied size classifications for subvisible (10?μm to 100?μm) and visible (=100?μm) particulate matter are adopted. 1.5 For the validation requirements for particle quantification test methods, see Practice E3468. 1.6 Units\u2014The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard. 1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
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Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment - ASTM E3466-25 - ASTM International
West Conshohocken, PA, United States
Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment
ASTM E3466-25
Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment ASTM E3466-25
1.1 In this guide, guidance on the development of particle quantification test methods that determine the count and sizes of particulate matter present on the surfaces of single-use bioprocessing equipment (single-use systems (SUS)) applied in biopharmaceutical manufacturing processes is described. 1.2 In particle quantification test methods, liquid is applied to extract particulate matter from the surfaces of SUS, and the extract is subsequently analyzed with a particle measurement technique to determine particle count and sizes. 1.3 This guide is limited to the application of the particle measurement techniques described in the pharmacopoeia for parenteral drug products: light obscuration (LO), membrane microscopy (MM), and flow imaging (FI). 1.4 In this guide, the commonly applied size classifications for subvisible (10?μm to 100?μm) and visible (=100?μm) particulate matter are adopted. 1.5 For the validation requirements for particle quantification test methods, see Practice E3468. 1.6 Units\u2014The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard. 1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

1.1 In this guide, guidance on the development of particle quantification test methods that determine the count and sizes of particulate matter present on the surfaces of single-use bioprocessing equipment (single-use systems (SUS)) applied in biopharmaceutical manufacturing processes is described.


1.2 In particle quantification test methods, liquid is applied to extract particulate matter from the surfaces of SUS, and the extract is subsequently analyzed with a particle measurement technique to determine particle count and sizes.


1.3 This guide is limited to the application of the particle measurement techniques described in the pharmacopoeia for parenteral drug products: light obscuration (LO), membrane microscopy (MM), and flow imaging (FI).


1.4 In this guide, the commonly applied size classifications for subvisible (10?μm to 100?μm) and visible (=100?μm) particulate matter are adopted.


1.5 For the validation requirements for particle quantification test methods, see Practice E3468.


1.6 Units\u2014The values stated in SI units are to be regarded as the standard. No other units of measurement are included in this standard.


1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.


1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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  ASTM International
Product Category Standards and Technical Documents
Product Number ASTM E3466-25
Product Name Standard Guide for Development of Test Methods for the Counting and Sizing of Particulate Matter on the Surfaces of Single-Use Bioprocessing Equipment
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