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 - 2019 EDITION - 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)

11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)

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)