The paper considers the issue related to calibration of conveyor weigher in laboratory environment for its usage as etalon and the subsequent transfer of a unit of linear density from them to the transported means of comparison – the measure of linear density. The equations of the mass flow in instant hopper-conveyor system are got. The algorithm of etalon conveyor weigher calibration is developed on the results of mass measurement in hopper at work process of hopper-conveyor instant system which doesn’t require passing a known fixed mass through a conveyor weigher. The transfer way of linear density unit from etalon conveyor weigher to linear density measure with accuracy required by measurement chain is proposed.

The results of the development of a gas mixing and analytical stand (reference complex) for testing in order to approve the type of automatic measuring systems (AMS) for determining the content of pollutants in industrial emissions are presented. During the use of the AMS test bench, the units of molar fraction and mass concentration are transferred from the State primary standard of units of molar fraction, mass fraction and mass concentration of components in gas and gas condensate media GET 154 to the tested measuring gas channels of AMS, thereby ensuring traceability of AMS measurement results to the State primary standard GET 154.

The authors of the publication have described the basic principles of the procedure of defining metrological characteristics of certified reference materials (hereinafter referred to as CRMs) of antibacterial substances that are being developed. CRMs of antibacterial substances are intended for certification of measurement procedures and accuracy control of measurement results. CRMs can be used for graduation, calibration of measuring instruments if their metrological and technical characteristics comply with the procedures of graduation and calibration of measuring instruments, as well as determination of antibiotic sensitivity of pathogenic microorganisms and authenticity of active substances in pharmaceutical drugs.