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ISO 13408-1:2008

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

General information

Withdrawn from 15.08.2023
Directives or regulations
None

Standard history

Status
Date
Type
Name
15.08.2023
Main
17.04.2013
Amendment
10.06.2008
Main
Main
ISO 13408-1:1998
ISO 13408-1:2008 specifies the general requirements for, and offers guidance on, processes, programmes and procedures for development, validation and routine control of the manufacturing process for aseptically-processed health care products.
ISO 13408-1:2008 includes requirements and guidance relative to the overall topic of aseptic processing. Specific requirements and guidance on various specialized processes and methods related to filtration, lyophilization, clean-in place (CIP) technologies, sterilization in place (SIP) and isolator systems are given in other parts of ISO 13408.

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