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ISO 13408-2 PDF

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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Association for the Advancement of Medical Instrumentation

We use cookies to make our website easier to use and to better understand your needs. Standards Subsctiption may be the perfect solution. Quality control, Quality assurance systems, Personnel, Environment workingBiological filters, Medical equipment, Verification, Filtration, Filters, Sterile equipment, Production, Sterilization hygieneQuality management. Click to learn more. Please download Chrome or 113408-2 or view our browser tips.

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You may delete a document from your Alert Profile at any time. The process include the filtration, lyophilization drying processclean-in-place technology CIPsterilization in iiso SIP and isolator system used to maintain aseptic conditions.

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EN ISO 13408-2

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

Please first log in with a verified email before subscribing to alerts. An alternative to terminal sterilization, asseptic processing enables the sterility of pre-sterilized components and products during assembly allowing the final product to be sterile in its final container resulting in an terminally sterilized product. This website is best viewed with browser version of up to Microsoft Internet Explorer 8 or Firefox 3. The faster, easier way to work with standards.