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ISO 13408-6:2021
2021
Aseptic processing of health care products – Part 6: Isolator systems
- Format:
- Language(s) :
- Published :
- English
- 04/01/2021
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.
| ISO 13408-6:2021 | |
|---|---|
| STANDARD INFO: | |
| Standard Name | ISO 13408-6:2021 |
| Scope | Aseptic processing of health care products - Part 6: Isolator systems |
| Publisher | ISO - International Organization for Standardization |
| Languages | English |
| State | |
| Publication Year | 2021 |
| Most recent Version | MOST RECENT |
| Whether to be replaced | |
| Addendum | |
| FILE INFO: | |
| File Size | 1 file , 1.5 MB |
| Note | This product is unavailable in Ukraine, Russia, Belarus |
| Published | 04/01/2021 |
| ISO 13408-6:2021 | ||
|---|---|---|
| History | Publisher Year | |
| ISO 13408-6:2021 | 2021 | Current |
| ISO 13408-6:2005 | 2005 |
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- Format:
- Language(s) :
- Published :
- English
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