Abstract
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.
General information
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Status: WithdrawnPublication date: 2008-06Stage: Withdrawal of International Standard [95.99]
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Edition: 2Number of pages: 45
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Technical Committee :ISO/TC 198ICS :11.080.01
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Life cycle
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Previously
WithdrawnISO 13408-1:1998
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Now
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00
Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Amendments
Provide additional content; available for purchase; not included in the text of the existing standard.WithdrawnISO 13408-1:2008/Amd 1:2013
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00
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Revised by
PublishedISO 13408-1:2023