International Standard
ISO 13408-6:2021
Aseptic processing of health care products — Part 6: Isolator systems
Reference number
ISO 13408-6:2021
Edition 2
2021-04
International Standard
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ISO 13408-6:2021
72836
Published (Edition 2, 2021)

ISO 13408-6:2021

ISO 13408-6:2021
72836
Language
Format
CHF 129
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Abstract

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.

General information

  •  : Published
     : 2021-04
    : International Standard published [60.60]
  •  : 2
     : 25
  • ISO/TC 198
    11.080.01 
  • RSS updates

Sustainable Development Goals

This standard contributes to the following Sustainable Development Goal

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