SS-EN-ISO-11138-7 › Sterilization of health care products - Biological indicators - Part 7: Guidance for the selection, use and interpretation of results (ISO 11138-7:2019)
SS-EN-ISO-11138-7
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2019 EDITION
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CURRENT
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This document provides guidance for the selection, use and interpretation of results from application of biological indicators when used in the development, validation and routine monitoring of sterilization processes. It does not consider those processes that rely solely on physical removal of microorganisms, e.g. filtration. It is not applicable to combination processes using, for example, washer-disinfectors or flushing and steaming of pipelines. It does not specify requirements for the selection and use of biological indicators intended to monitor vaporised hydrogen peroxide processes for isolator and room biodecontamination processes at atmospheric pressure. It is not applicable to liquid immersion sterilization processes.
To find similar documents by classification:
11.040.01 (Medical equipment in general)
11.120.01 (Pharmaceutics in general)
Medical devices
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Designation Name
SS-EN ISO 11138-7:2019
Revision Level
2019 EDITION
Status
Current
Publication Date
April 24, 2019
Language(s)
English
Page Count
80
International Equivalent
EN ISO 11138-7:2019(IDT); ISO 11138-7:2019(IDT)