Narrow Your Results
NOTE: This guide specification covers the requirements for automatic dosing siphons for sewage.
Preface The field of nanoscience has experienced unprecedented growth during the last few years and as a result has received a great deal of attention from the public, regulatory agencies, and the science community. However, there are many challenges that must be overcome before we can apply...
Personnel monitoring is a term designating the determination of the inhaled dose of an airborne toxic material of an air-mediated hazardous physical force by the continuous collection of samples in the breathing or auditory zone, or auditory zone, or other appropriate exposed body area, over...
This European Standard specifies definitions, principles of construction (but not dimensions) and design, requirements on performance and operation as well as methods for testing the performance of adjustable chemical dosing systems for conditioning water intended for human consumption...
This European Standard specifies definitions, principles of construction (but not dimensions) and design, requirements on performance and operation as well as methods for testing the performance of chemical pre-set dosing systems for conditioning water intended for human consumption inside...
This document specifies requirements for sterile single-use hypodermic syringes of nominal capacity 1 ml and above, made of plastic materials and intended for use with power-driven syringe pumps. This document does not apply to syringes with auto-disable syringe features (ISO 7886-3[2]),...
This document provides guidance regarding the preparation of nanomaterials for eco- and biotoxicological testing. It provides guidance regarding factors pertaining to sample preparation and dose determination that might be useful in toxicological, including ecotoxicological, testing of...
ISO/TR 16196:2016 provides guidance regarding the preparation of nanomaterials for eco- and bio- toxicological testing. It provides guidance regarding factors pertaining to sample preparation and dose determination that might be useful in toxicological, including ecotoxicological, testing of...
4.1 Obtaining samples of high-level waste created during the reprocessing of spent nuclear fuels presents unique challenges. Generally, high-level waste is stored in tanks with limited access to decrease the potential for radiation exposure to personnel. Samples must be obtained remotely because of...
This document specifies the performance and testing of DOSE AREA PRODUCT METERS intended to measure DOSE AREA PRODUCT and/or DOSE AREA PRODUCT RATE to which the PATIENT is exposed during MEDICAL RADIOLOGICAL EXAMINATIONS. This document is applicable to the following types of...
4.1 Obtaining samples of high-level waste created during the reprocessing of spent nuclear fuels presents unique challenges. Generally, high-level waste is stored in tanks with limited access to decrease the potential for radiation exposure to personnel. Samples must be obtained remotely because of...
This document specifies the performance and testing of DOSE AREA PRODUCT METERS intended to measure DOSE AREA PRODUCT and/or DOSE AREA PRODUCT RATE to which the PATIENT is exposed during MEDICAL RADIOLOGICAL EXAMINATIONS. This document is applicable to the following types of...
This document specifies the performance and testing of DOSE AREA PRODUCT METERS intended to measure DOSE AREA PRODUCT and/or DOSE AREA PRODUCT RATE to which the PATIENT is exposed during MEDICAL RADIOLOGICAL EXAMINATIONS. This document is applicable to the following types of...
IEC 60580:2019 is available as IEC 60580:2019 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.IEC 60580:2019 specifies...
This part of ISO 11137 specifies methods of determining the minimum dose needed to achieve a specified requirement for sterility and methods to substantiate the use of 25 kGy or 15 kGy as the sterilization dose to achieve a sterility assurance level, SAL, of 10-6. This part of ISO...
This practice is intended to determine the potential for a substance, or material extract, to elicit contact dermal allergenicity. It is intended as an alternative to the Guinea Pig Maximization Test (GPMT), given the limitations on dosage form and tendency for false positives associated with the...
