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ASTM E1367-03(2023) - Standard Test Method for Measuring the Toxicity of Sediment-Associated Contaminants with Estuarine and Marine Invertebrates
January 1, 2023 - ASTM International

5.1 General: 5.1.1 Sediment provides habitat for many aquatic organisms and is a major repository for many of the more persistent chemicals that are introduced into surface waters. In the aquatic environment, most anthropogenic chemicals and waste materials including toxic organic and inorganic...

BS EN ISO 18472 - Sterilization of health care products - Biological and chemical indicators - Test equipment
September 30, 2018 - BSI
A description is not available for this item.
ASTM D2331-08(2022) - Standard Practices for Preparation and Preliminary Testing of Water-Formed Deposits
July 1, 2022 - ASTM International

4.1 Deposits in piping from aqueous process streams serve as an indicator of fouling, corrosion or scaling. Rapid techniques of analysis are useful in identifying the nature of the deposit so that the reason for deposition can be ascertained. 4.2 Possible treatment schemes can be devised to...

DS/ISO 11737-2 - Sterilization of medical devices – Microbiological methods – Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
May 18, 2020 - DS

1.1 This document specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent reduced relative to that anticipated to be used in routine sterilization processing. These tests are intended to be performed when defining,...

DS/EN ISO 11737-2 - Sterilization of health care products – Microbiological methods – Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
May 18, 2020 - DS

1.1 This document specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent which has been reduced relative to that anticipated to be used in routine sterilization processing. These tests are intended to be performed...

ASTM E2122-22 - Standard Guide for Conducting In-situ Field Bioassays With Caged Bivalves
April 1, 2022 - ASTM International

1.1 This guide describes procedures for conducting controlled experiments with caged bivalves under field conditions. The purpose of this approach is to facilitate the simultaneous collection of field data to help characterize chemical exposure and associated biological effects in the same...

AAMI ST21 - Biological Indicators for Ethylene Oxide Sterilization Process in Health Care Facilities
October 1, 1986 - AAMI
A description is not available for this item.
DS/ISO/TS 21387 - Sterilization of medical devices – Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
September 21, 2020 - DS

This document provides guidance on the requirements of ISO 11135 that apply when parametric release is used to release the product after exposure to the sterilization process. It provides a path for transition of existing cycles, as well as a path for the development and implementation of a...

ISO 11737-2 - Sterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
December 1, 2019 - ISO

This document specifies the general criteria for tests of sterility on medical devices that have been exposed to a treatment with the sterilizing agent which has been reduced relative to that anticipated to be used in routine sterilization processing. These tests are intended to be performed when...

DSF/FPREN ISO 11138-7 - Sterilization of health care products – Biological indicators – Part 7: Guidance for the selection, use and interpretation of results (ISO/FDIS 11138-7:2018)
DS

This International Standard 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. 1.1 Exclusions This International Standard does not...

ISO TS 21387 - Sterilization of medical devices — Guidance on the requirements for the validation and routine processing of ethylene oxide sterilization processes using parametric release
September 1, 2020 - ISO

This document provides guidance on the requirements of ISO 11135 that apply when parametric release is used to release the product after exposure to the sterilization process. It provides a path for transition of existing cycles, as well as a path for the development and implementation of a...

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