Abstract
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) and isolator systems are given in the other parts of the ISO 13408 series.
General information
-
Status: PublishedPublication date: 2023-08Stage: International Standard published [60.60]
-
Edition: 3Number of pages: 72
-
Technical Committee :ISO/TC 198ICS :11.080.01
- RSS updates
Life cycle
-
Previously
WithdrawnISO 13408-1:2008
WithdrawnISO 13408-1:2008/Amd 1:2013
-
Now