• ASTM E 2474 : 2014 : REDLINE

    Current The latest, up-to-date edition.

    Standard Practice for Pharmaceutical Process Design Utilizing Process Analytical Technology

    Available format(s):  PDF

    Language(s):  English

    Published date:  01-04-2014

    Publisher:  American Society for Testing and Materials

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    Abstract - (Show below) - (Hide below)

    CONTAINED IN VOL. 13.01, 2017 Defines process design, which is integral to process development as well as post-development process optimization.

    Scope - (Show below) - (Hide below)

    1.1This practice covers process design, which is integral to process development as well as post-development process optimization. It is focused on practical implementation and experimental development of process understanding.

    1.2The term process design as used in this practice can mean:

    1.2.1The activities to design a process (the process design), or

    1.2.2The outcome of this activity (the designed process), or both.

    1.3The principles in this practice are applicable to both drug substance and drug product processes. For drug products, formulation development and process development are interrelated and therefore the process design will incorporate knowledge from the formulation development.

    1.4The principles in this practice apply during development of a new process or the improvement or redesign of an existing one, or both.

    1.5This 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 and health practices and determine the applicability of regulatory limitations prior to use.

    General Product Information - (Show below) - (Hide below)

    Committee E 55
    Document Type Redline
    Publisher American Society for Testing and Materials
    Status Current

    Standards Referenced By This Book - (Show below) - (Hide below)

    ASTM E 2891 : 2013 Standard Guide for Multivariate Data Analysis in Pharmaceutical Development and Manufacturing Applications
    ASTM E 2476 : 2016 : REDLINE Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture
    ASTM E 2475 : 2010 Standard Guide for Process Understanding Related to Pharmaceutical Manufacture and Control
    ASTM E 2500 : 2013 : REDLINE Standard Guide for Specification, Design, and Verification of Pharmaceutical and Biopharmaceutical Manufacturing Systems and Equipment
    ASTM E 2475 : 2010 : R2016 Standard Guide for Process Understanding Related to Pharmaceutical Manufacture and Control

    Standards Referencing This Book - (Show below) - (Hide below)

    ASTM E 2629 : 2011 Standard Guide for Verification of Process Analytical Technology (PAT) Enabled Control Systems
    ASTM E 2476 : 2016 : REDLINE Standard Guide for Risk Assessment and Risk Control as it Impacts the Design, Development, and Operation of PAT Processes for Pharmaceutical Manufacture
    ASTM E 2587 : 2016 : REDLINE Standard Practice for Use of Control Charts in Statistical Process Control
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