ISO 13408-6:2021
Current
The latest, up-to-date edition.
Aseptic processing of health care products Part 6: Isolator systems
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
English, French
13-04-2021
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This document specifies the requirements for and provides guidance on the specification, selection, qualification, bio-decontamination, validation, operation and control of isolator systems related to aseptic processing of health care products and processing of cell-based health care products.
This document does not specify requirements for restricted access barrier systems (RABS).
This document does not supersede or replace national regulatory requirements such as Good Manufacturing Practices (GMPs) and/or compendia requirements that pertain in particular to national or regional jurisdictions.
This document does not specify requirements for isolators used for sterility testing; however, some of the principles and information in this document could be applicable to this application.
This document does not define biosafety containment requirements.
| DocumentType |
Standard
|
| Pages |
25
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| SN EN ISO 13408-6:2021 | Identical |
| ÖNORM EN ISO 13408-6:2021 10 15 | Identical |
| I.S. EN ISO 13408-6:2021 | Identical |
| PN-EN ISO 13408-6:2021-10 | Identical |
| NF EN ISO 13408-6:2021 | Identical |
| UNI EN ISO 13408-6:2021 | Identical |
| PN-EN ISO 13408-6:2021-10/Ap1:2023-03 | Identical |
| BS EN ISO 13408-6:2021 | Identical |
| I.S. EN ISO 13408-6:2021&LC:2021 | Identical |
| UNE-EN ISO 13408-6:2022 | Identical |
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