Systèmes de récupération des vapeurs dans les réseaux de distribution d’essence
1 Objet
La présente Norme nationale du Canada définit les exigences relatives à l’équipement, aux critères de rendement,
à la procédure à suivre et aux méthodes d’essai pour la mise en place de systèmes de récupération des vapeurs
(SRV) dans les réseaux de distribution d’essence comprenant des terminaux, des dépôts routiers, des stationsservice
et des camions-citernes qui sont couramment…
Radiological protection — Criteria and performance limits for the periodic evaluation of dosimetry s...
The quality of a supplier of a dosimetry service depends on both the characteristics of the approved (type‑tested) dosimetry system[1] and the training and experience of the staff, together with the calibration procedures and quality assurance programmes.
This document specifies the criteria and the test procedures to be used for the periodic verification of the performance of dosimetry services…
Recommendations for renewable energy and hybrid systems for rural electrification - Part 9-5: Integr...
IEC TS 62257-9-5:2018 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 TS 62257-9-5:2018 applies to stand-alone renewable energy products. This document deals essentially with off…
Recommendations for renewable energy and hybrid systems for rural electrification - Part 9-5: Integr...
IEC TS 62257-9-5:2018 applies to stand-alone renewable energy products. This document deals essentially with off-grid renewable energy products with batteries and solar modules with DC system voltages not exceeding 35 V and peak power ratings not exceeding 350 W. The tests contained herein are capable in many cases of adequately assessing systems at higher voltages and/or power ratings. This new…
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 031:...
IEC 61010-031:2015+A1:2018 specifies safety requirements for hand-held and hand-manipulated probe assemblies of the types described below, and their related accessories. These probe assemblies are for direct electrical connection between a part and electrical test and measurement equipment. They may be fixed to the equipment or be detachable accessories for the equipment. It has the status of a…
Safety requirements for electrical equipment for measurement, control and laboratory use - Part 031:...
IEC 61010-031:2015+A1:2018 specifies safety requirements for hand-held and hand-manipulated probe assemblies of the types described below, and their related accessories. These probe assemblies are for direct electrical connection between a part and electrical test and measurement equipment. They may be fixed to the equipment or be detachable accessories for the equipment. It has the status of a…
Vacuum technology — Vacuum gauges — Characterization of quadrupole mass spectrometers for partial pr...
This document describes procedures to characterize quadrupole mass spectrometers (QMSs) with an ion source of electron impact ionization and which are designed for the measurement of atomic mass-to-charge ratios m/z < 300.
This document is not applicable to QMSs with other ion sources, such as chemical ionization, photo-ionization or field ionization sources and for the measurements of higher…
Requirements for the design, development, and validation of laboratory-developed tests used for the ...
1 Scope
1.1 General
This Standard specifies the minimum requirements and best practices for the development, validation, and use of laboratory-developed tests in clinical and research laboratories for the screening, diagnosis, and management of clinical conditions.
It does not provide specific details on how to achieve these requirements since they are provided in many other sources which are…
Safety requirements for electrical equipment for measurement, control, and laboratory use — Part 2-2...
This clause of Part 1 is applicable, except as follows.
1.1.1 Equipment included in scope
Replacement:
• This part of IEC 61010 specifies safety requirements and related verification tests for any
product performing the function of control equipment and/or their associated peripherals.
In addition, these products have as their intended use the command and control of
machines, automated…
1.1
This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical
devices at each phase of the reprocessing workflow, including
a) establishing a QMS for the MDRD, including
i) key performance indicators;
ii) policies and procedures;
iii) documentation;
iv) roles and responsibilities;
v) management review;
vi) planning, resources and operations…