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This document describes general workflows and protocols for the validation and the verification of qualitative screening tests for the detection of residues of veterinary drugs in liquid milk (raw, pasteurized, UHT and reconstituted milk powders and whey protein extracts) including biological methods. This guideline does not cover the validation of residue analysis by HPLC, UHPLC or LC-MS/MS.…

This document specifies three procedures to test the service life of a blast-cleaning abrasive under laboratory conditions. The performance of an abrasive is also measured by its ability to clean, via transmission of kinetic energy to the substrate in the blasting process. This document also specifies the procedures that can be performed in the same testing machines to help evaluate abrasive…

1 Scope This document defines methods for reducing combined samples (or increments) to laboratory samples and laboratory samples to sub-samples and general analysis samples and is applicable to solid biofuels. The methods defined in this document can be used for sample preparation, for example, when the samples are to be tested for calorific value, moisture content, ash content, bulk density…

1 Scope 1.1 General This Standard pertains to the characterization of radioactive waste and irradiated fuel. This Standard a) specifies the overall requirements for establishing and implementing a waste characterization strategy, program, and plan; b) specifies methodologies for the sampling and characterization of radioactive waste and irradiated fuel; c) provides guidance for the timing…

This document specifies procedures and test methods used to demonstrate the cleaning efficacy of washer-disinfectors (WD) and their accessories intended to be used for cleaning of reusable medical devices. NOTE 1   The requirements can be used for washer-disinfectors intended for use with other articles used in the context of medical, dental, laboratory, pharmaceutical and veterinary practice.…

This document specifies a bioassay for the determination of the presence of unknown toxic contaminants in test seawater (see Figure A.1). It is based on the inhibition of photosynthetic activity of the marine cyanobacterium Cyanobium sp. (NIES-981) by such toxic contaminants. The inhibition is determined based on delayed fluorescence (DF) intensity. The method is rapid and requires less…

This document specifies requirements and gives recommendations for the collection, handling, documentation, transport, storage and processing during the pre-examination phase of formalin-fixed and paraffin-embedded (FFPE) tissue specimens intended for qualitative and/or (semi-)quantitative in situ examination of the morphology and of biomolecules, such as metabolites, proteins, DNA and/or RNA, on…

Scope Replacement: This part of IEC 80601 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SCREENING THERMOGRAPHS intended to be used for the individual non-invasive febrile temperature screening of a human under controlled environmental conditions, hereafter referred to as ME EQUIPMENT. This document sets laboratory characterization test limits for the SCREENING THERMOGRAPH. NOTE…

Scope Replacement: This document applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PULSE OXIMETER EQUIPMENT intended for use on humans, hereafter referred to as ME EQUIPMENT. This includes any part necessary for NORMAL USE, including the PULSE OXIMETER MONITOR, PULSE OXIMETER PROBE, and PROBE CABLE EXTENDER. These requirements also apply to PULSE OXIMETER EQUIPMENT, including PULSE…