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Standard

SN EN ISO 13408-2:2018

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Astratto

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.

Specifiche dei prodotti

  • Standard da INB
  • Pubblicato:
  • Efficace:
  • Tipo di documento: EN
  • Pagine
  • ICS 11.080.01
  • Publisher SNV
  • Distributor SNV
  • National Committee INB/NK 171
  • European TC CEN/TC 204
  • International TC ISO/TC 198

Riferimento legale

Autorità federale svizzera: SWISSMEDIC
Designato ai sensi della legge svizzera:
Riferimento legaleRestrizioni
812.213
Designato ai sensi della legislazione dell'UE:
Riferimento legaleRestrizioni
90/385/EWG
Council Directive 93/42/EEC
98/79/EG

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