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This document describes the design, use and calibration of volumetric measures (capacity measures) which are intended for use in fixed locations in a laboratory or in the field. This document gives guidance on both standard and non-standard measures. It also covers portable and mobile measures. This document is applicable to the petroleum industry; however, it may be applied more widely to other…

1.1 This document — specifies basic methods for estimating the bias of a measurement method and the laboratory bias when a measurement method is applied; — provides a practical approach of a basic method for routine use in estimating the bias of measurement methods and laboratory bias; — provides a brief guidance to all personnel concerned with designing, performing or analysing the…

This document specifies the application, in the context of traditional Chinese medicine practice, of medical waveform format encoding rules (MFER) to pulse condition waveform as measured in physiological laboratories, hospitals, bed-wards, pharmacies, clinics, community health centres and home care check-ups using pulse condition devices.

1.1 This Standard has been developed for the assessment of volatile organic compound emissions from polyurethane foam materials used in residential and nonresidential occupancies. It outlines a test procedure for the determination of volatile organic compounds from the specimen and explains why certain test conditions have been selected. 1.2 This laboratory test method is based on ASTM D5116…

This document specifies dimensional and other requirements for the 11 most commonly used carbide cutters which are predominantly used in the dental laboratory. NOTE These cutters are also used in podiatry.

1 Scope 1.1 This Standard sets forth characteristics of effective and durable installation methods, in both new and existing buildings, of fenestration products within the scope of AAMA/WDMA/CSA 101/I.S.2/A440 that are intended for installation in buildings of all occupancies to which NBC Parts 3, 4, 5, and 6 of Division B apply. 1.2 In addition to fenestration products within the scope of…

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This document specifies a process for a medical laboratory to identify and manage the risks to patients, laboratory workers and service providers that are associated with medical laboratory examinations. The process includes identifying, estimating, evaluating, controlling and monitoring the risks. The requirements of this document are applicable to all aspects of the examinations and services of…

1.1 This document specifies, in accordance with ISO 10326‑1:2016, a laboratory method for measuring and evaluating the effectiveness of the seat suspension in reducing the vertical whole-body vibration transmitted to the operator of earth-moving machines at frequencies between 1 Hz and 20 Hz. It also specifies acceptance criteria for application to seats on different machines. 1.2 This document…

This document specifies requirements for safe practices in the medical laboratory (herein after referred to as "the laboratory").