ISO 13408-1:2023

Current Revision
Aseptic processing of health care products - Part 1: General requirements

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Aseptic processing of health care products - Part 1: General requirements

PUBLISH DATE 2023

This document specifies the general requirements for, and offers guidance on, processes, programs and procedures for development, validation and routine control of aseptic processing of health care products.

This document includes requirements and guidance relative to the overall topic of aseptic processing.

Specific requirements and guidance on various specialized processes and methods related to:

  • sterilizing filtration
  • lyophilization
  • clean-in place (CIP) technologies
  • sterilization in place (SIP)
  • isolator systems

are given in the other parts of the ISO 13408 series.

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