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ASTM E 2898 : 2020 : REV A

Current

Current

The latest, up-to-date edition.

Standard Guide for Risk-Based Validation of Analytical Methods for PAT Applications

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

10-08-2023

£48.38
Excluding VAT

Committee
E 55
DocumentType
Guide
Pages
7
PublisherName
American Society for Testing and Materials
Status
Current
Supersedes

1.1This guide provides an overview to the risk-based validation of process analytical methods under a process analytical technology (PAT) paradigm for pharmaceuticals and biopharmaceuticals and as such includes guidance on assessing risk to product quality from inappropriate method validation.

1.2This guide builds on existing standards on the topic of validation concentrating on applying such standards to analytical methods for on-line analysis. In particular, it addresses the validation of at-line, on-line, or in-line PAT measurements and covers both drug substance and drug product (DP) measurements.

1.3The definitions of International Council for Harmonisation (ICH) validation parameters (such as specificity, precision, repeatability, etc.) apply; however, the method of demonstrating the validation parameters may vary from that described in ICH and is discussed.

1.4As consistent with the U.S. Food and Drug Administration (FDA) process validation guidance, this document also briefly covers ongoing assurance that the method remains in a validated state during routine use.

1.5Equipment and instrument qualification are out of the scope of this guide but will be referenced as inputs to validation of analytical methods for PAT applications.

1.6The validation of multivariate prediction models is out of scope but will be referenced as inputs to validation of analytical methods for PAT applications.

1.6.1The validation of any analytical model used in the PAT method is essential to the validation of the PAT method but, the details of the model validation process is out of scope. See term model validation, 3.1.7.

1.7Microbiological methods are out of scope.

1.8This 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.

1.9This 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.

ASTM E 3326 : 2022 Standard Guide for Application of Continuous Manufacturing (BioCM) in the Biopharmaceutical Industry
ASTM E 2968 : 2023 Standard Guide for Application of Continuous Manufacturing (CM) in the Pharmaceutical Industry
ASTM E 2629 : 2020 Standard Guide for Verification of Process Analytical Technology (PAT) Enabled Control Systems

ASTM D 6122 : 2021 Standard Practice for Validation of the Performance of Multivariate Online, At-Line, Field and Laboratory Infrared Spectrophotometer, and Raman Spectrometer Based Analyzer Systems
ASTM D 6122 : 2020 : REV A Standard Practice for Validation of the Performance of Multivariate Online, At-Line, Field and Laboratory Infrared Spectrophotometer, and Raman Spectrometer Based Analyzer Systems
ASTM E 2500 : 2020 Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
ASTM E 2656 : 2016 Standard Practice for Real-time Release Testing of Pharmaceutical Water for the Total Organic Carbon Attribute
ASTM D 3764 : 1992 : R1998 Standard Practice for Validation of Process Stream Analyzer Systems
ASTM D 6122 : 2019 : REV B Standard Practice for Validation of the Performance of Multivariate Online, At-Line, and Laboratory Infrared Spectrophotometer Based Analyzer Systems
ASTM E 2891 : 2020 Standard Guide for Multivariate Data Analysis in Pharmaceutical Development and Manufacturing Applications
ASTM E 2476 : 2016 Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture
ASTM D 3764 : 2019 Standard Practice for Validation of the Performance of Process Stream Analyzer Systems
ASTM D 3764 : 2022 Standard Practice for Validation of the Performance of Process Stream Analyzer Systems
ASTM D 6122 : 2023 Standard Practice for Validation of the Performance of Multivariate Online, At-Line, Field and Laboratory Infrared Spectrophotometer, and Raman Spectrometer Based Analyzer Systems
ASTM D 3764 : 2023 Standard Practice for Validation of the Performance of Process Stream Analyzer Systems
ASTM E 2476 : 2022 Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture
ASTM E 2629 : 2020 Standard Guide for Verification of Process Analytical Technology (PAT) Enabled Control Systems
ASTM D 6122 : 2022 Standard Practice for Validation of the Performance of Multivariate Online, At-Line, Field and Laboratory Infrared Spectrophotometer, and Raman Spectrometer Based Analyzer Systems

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