Published
ISO 13408-2:2018 specifies requirements for sterilizing filtration as part of aseptic processing of health care products conducted in accordance with ISO 13408‑1. It also offers guidance to filter users concerning general requirements for set-up, validation and routine operation of a sterilizing filtration process.
ISO 13408-2:2018 is not applicable to removal of viruses.
Sterilizing filtration is not applicable to fluids that intentionally contain particles larger than the pore size of the filter (e.g. bacterial whole-cell vaccines).
ISO 13408-2:2018 is not applicable to high efficiency particulate air (HEPA) filters.
ISO 13408-2:2018 does not specify requirements for the development, validation and routine control of a process for removing the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. Specific recommendations have been produced in particular countries for the processing of materials potentially contaminated with these agents.
                WITHDRAWN
                                    ISO 13408-2:2003
                            
                    PUBLISHED
                    ISO 13408-2:2018
                    90.93
                                        Standard confirmed
                    Jan 31, 2024
                
                    PROJECT
                                            ISO 13408-2:2018/DAmd 1
                                    
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)
60.60 Standard published