Household and similar electrical appliances - Test code for the determination of airborne acoustical...
IEC 60704-2-14:2013+A1:2019 specifies the measuring conditions to provide for sufficient accuracy in determining the noise emitted and comparing the results of measurements taken by different laboratories, whilst simulating as far as possible the practical use of household refrigerators, frozen-food storage cabinets and food freezers. It is recommended to consider the determination of noise…
IEC 61315:2019 is applicable to instruments measuring radiant power emitted from sources that are typical for the fibre-optic communications industry. These sources include laser diodes, light emitting diodes (LEDs) and fibre-type sources. Both divergent and collimated radiations are covered. This document defines the calibration of power meters to be performed by calibration laboratories or by…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
IEC 61010-2-011:2019 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition.
IEC 61010-2-011:2019 specifies particular safety requirements for the following types a) to c) of electrical…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
IEC 61010-2-011:2019 specifies particular safety requirements for the following types a) to c) of electrical equipment and their accessories, wherever they are intended to be used, whenever that equipment incorporates refrigerating systems as an integral part of, or separate from, the equipment and the equipment is in direct control of the refrigerating system. This document details all the…
Radiological protection — Performance criteria for laboratories using Fluorescence In Situ Hybridiza...
The purpose of this document is to provide criteria for quality assurance (QA), quality control (QC) and evaluation of the performance of biological dosimetry by cytogenetic service laboratories.
This document addresses:
a) the responsibilities of both the customer and the laboratory;
b) the confidentiality of personal information, for the customer and the laboratory;
c) the laboratory…
Alpine and touring ski-bindings — Test soles for ski-binding tests
This document defines test soles representing
— an alpine ski-boot (form A) or at least the bottom part of it to be used for testing alpine ski-bindings for alpine skiing in accordance with ISO 9462 and ISO 9465, and
— a touring ski-boot (form T) or at least the bottom part of it to be used for testing touring ski-bindings for touring skiing in accordance with ISO 13992 and ISO…
Determination of the ultimate aerobic biodegradability of plastic materials in an aqueous medium — M...
This document specifies a method, by measuring the oxygen demand in a closed respirometer, for the determination of the degree of aerobic biodegradability of plastic materials, including those containing formulation additives. The test material is exposed in an aqueous medium under laboratory conditions to an inoculum from activated sludge.
If an unadapted activated sludge is used as the inoculum…
Water quality — Gross alpha and gross beta activity — Test method using thin source deposit
This document specifies a method for the determination of gross alpha and gross beta activity concentration for alpha- and beta-emitting radionuclides. Gross alpha and gross beta activity measurement is not intended to give an absolute determination of the activity concentration of all alpha and beta emitting radionuclides in a test sample, but is a screening analysis to ensure particular…
Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous...
This document gives guidelines on the handling, storage, processing and documentation of venous whole blood specimens intended for cellular RNA examination during the pre-examination phase before a molecular examination is performed. This document covers specimens collected in venous whole blood collection tubes.
This document is applicable to any molecular in vitro diagnostic examination…