Reference number
ISO 13408-7:2012
ISO 13408-7:2012
© ISO 2024
International Standard
ISO 13408-7:2012
Aseptic processing of health care products — Part 7: Alternative processes for medical devices and combination products
Edition 1
2012-08
2012-08
ISO 13408-7:2012
30061
Published
(Edition 1, 2012)
This publication was last reviewed and confirmed in 2023.
Therefore this version remains current.
Abstract
ISO 13408-7:2012 specifies requirements and provides guidance on alternative approaches to process simulations for the qualification of the aseptic processing of medical devices and combination products that cannot be terminally sterilized and where the process simulation approach according to ISO 13408-1 cannot be applied.
ISO 13408-7:2012 describes how risk assessment can be used during the development of an aseptic process to design a process simulation study for medical devices and combination products in those cases where a straightforward substitution of media for product during aseptic processing is not feasible or would not simulate the actual aseptic process.
General information
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Status: PublishedPublication date: 2012-08Stage: International Standard confirmed [90.93]
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Edition: 1Number of pages: 19
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Technical Committee :ISO/TC 198ICS :11.080.01
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