ISO 13408-1:2023
Current
The latest, up-to-date edition.
Aseptic processing of health care products — Part 1: General requirements
Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users
English, French
15-08-2023
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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 ISO13408 series.
| Committee |
ISO/TC 198
|
| DocumentType |
Standard
|
| Pages |
72
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| ANSI/AAMI/ISO 13408-1:2023 | Identical |
| PN-EN ISO 13408-1:2024-10 | Identical |
| NS-EN ISO 13408-1:2024 | Identical |
| DS/ISO 13408-1:2023 | Identical |
| SN EN ISO 13408-1:2024 | Identical |
| DS/EN ISO 13408-1:2024 | Identical |
| UNI EN ISO 13408-1:2024 | Identical |
| PNE-EN ISO 13408-1 | Identical |
| ÖNORM EN ISO 13408-1:2024 10 15 | Identical |
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