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I.S. EN ISO () (English): Aseptic processing of health care products – Part 2: Filtration [Authority: The European Union Per. BS EN ISO specifies requirements for sterilizing filtration as part of aseptic processing of health care products conducted in. ANSI/AAMI/ISO (R)/A ANSI/AAMI/ISO ANSI/AAMI/ISO (R) ANSI/AAMI/ISO (R).

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An alternative to terminal sterilization, asseptic processing enables the sterility of pre-sterilized components and products during 1340-82 allowing the final product to be sterile in its final container resulting in an terminally sterilized product. Learn more about the cookies we use and how to change your settings. The process include the filtration, lyophilization drying processclean-in-place technology CIPsterilization in place SIP and isolator system used to maintain aseptic conditions.

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BS EN ISO 13408-2:2018

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If the document is revised or amended, you will be notified by email. You may experience issues viewing this site in Internet Explorer 9, 10 or Quality control, Quality assurance systems, Personnel, Environment isiBiological filters, Medical equipment, Verification, Filtration, Filters, Sterile equipment, Production, Sterilization hygieneQuality management. Accept and continue 133408-2 more about the cookies we use and how to change your settings.

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EN ISO 13408-2

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ISO – Aseptic processing of health care products — Part 2: Sterilizing filtration

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