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Overview ISO 11138-1:2017 - Sterilization of health care products: Biological indicators - Part 1: General requirements defines the basic, common requirements for biological indicators (BIs) used in…
Overview ISO 1113:1979 specifies the representation of the 7-bit coded character set on punched tape 25.4 mm (1 in) wide. The standard is intended for use in conjunction with ISO 646 (the 7-bit chara…
Overview ISO 11137-2:2013 - “Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose” specifies validated methods to determine the minimum radiation dose requi…
Overview ISO 11138-2:2017 specifies requirements and test methods for biological indicators (BIs) used to assess sterilizers and sterilization processes that employ ethylene oxide (EO) gas. The stand…
Overview ISO 11138-3:2017 - "Sterilization of health care products - Biological indicators - Part 3" specifies technical requirements and test methods for biological indicators used to assess moist h…
Overview ISO 11138-4:2017 - "Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes" specifies requirements for biological…
Overview ISO 11130:2017 - "Corrosion of metals and alloys - Alternate immersion test in salt solution" specifies a laboratory method to assess corrosion resistance by repeatedly immersing metal speci…
Overview ISO 11132:2021 - Sensory analysis: Guidelines for measuring the performance of a quantitative descriptive sensory panel provides practical guidance for validating and monitoring the performa…
Overview EN ISO 11137-1:2026 is the key European and international standard for the radiation sterilization of health care products, specifically medical devices. Developed by CEN in alignment with I…
Overview SIST EN ISO 11137-1:2026 outlines the requirements for the development, validation, and routine control of radiation sterilization processes, specifically for medical devices. Radiation ster…
Overview ISO 11137-1:2025 - “Sterilization of health care products - Radiation - Part 1” defines requirements for the development, validation and routine control of radiation sterilization processes…
Overview ISO 11137-1:2006 - "Sterilization of health care products - Radiation - Part 1" defines the requirements for development, validation and routine control of radiation sterilization processes…
Overview ISO 11137-3:2017 - "Sterilization of health care products - Radiation - Part 3" provides non‑normative guidance on dosimetric aspects for the development, validation and routine control of r…
Overview ISO 11138-7:2019 - "Sterilization of health care products - Biological indicators - Part 7" provides practical guidance for the selection, use and interpretation of biological indicators (BI…
Overview ISO 11135:2014 - Sterilization of health‑care products - Ethylene oxide specifies the requirements for the development, validation and routine control of an ethylene oxide (EO) sterilization…
Overview ISO 11136:2014 - Sensory analysis - Methodology - General guidance for conducting hedonic tests with consumers in a controlled area provides standardized guidance for measuring how much cons…
Overview ISO 11138-8:2021 specifies a standardized test method to establish or confirm a Reduced Incubation Time (RIT) for biological indicators (BIs) used to monitor moist heat and ethylene oxide (E…
Overview ISO 11138-5:2017 - "Sterilization of health care products - Biological indicators - Part 5" - specifies requirements for biological indicators, inoculated carriers, suspensions, test organis…
Overview ISO 11139:2018 is the International Organization for Standardization (ISO) vocabulary for the sterilization of health care products. This first edition (2018) replaces ISO/TS 11139:2006 and…
Overview - What ISO 11133:2014 covers ISO 11133:2014 - "Microbiology of food, animal feed and water - Preparation, production, storage and performance testing of culture media" establishes requiremen…
1 Scope This International Standard gives guidelines for monitoring and assessing the overall performance of a quantitative descriptive panel and the performance of each member. A panel of assessors…