Abstract
ISO 13408-6:2005 specifies the requirements for isolator systems used for aseptic processing and offers guidance on qualification, bio-decontamination, validation, operation and control of isolator systems used for aseptic processing of health care products.
ISO 13408-6:2005 is focused on the use of isolator systems to maintain aseptic conditions; this may include applications for hazardous materials.
ISO 13408-6:2005 does not supersede or replace national regulatory requirements, such as Good Manufacturing Practices (GMPs) and/or compendial requirements that pertain in particular to national or regional jurisdictions.
General information
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Status: WithdrawnPublication date: 2005-06Stage: Withdrawal of International Standard [95.99]
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Edition: 1Number of pages: 17
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Technical Committee :ISO/TC 198ICS :11.080.01
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Life cycle
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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 13408-6:2005/Amd 1:2013
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00
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Revised by
PublishedISO 13408-6:2021