90.60 Close of review Sep 3, 2026
ISO
ISO/TC 198 Sterilization of health care products
International Standard
11.080.01 Sterilization and disinfection in general
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.
PUBLISHED
ISO 13408-6:2021
90.60
Close of review
Sep 3, 2026