Nanotechnologies — Toxicity assessment and bioassimilation of manufactured nano-objects in suspensio...
This document provides a reliable and repeatable method for simultaneous assessment of both exposure and toxicity of manufactured nano-objects (MNOs) using Tetrahymena sp. The ingested, internalized material (MNOs) indicates aquatic exposure.
This document is intended to be used by all the centers working with nano(eco)toxicity of MNOs and capable of culturing of Tetrahymena sp. The method uses…
Conveyor belts — Laboratory scale flammability characteristics — Requirements and test method
This document specifies a method for assessing, on a small scale, the reaction of a conveyor belt to an ignition flame source. It is applicable to conveyor belts having a textile carcass as well as steel cord conveyor belts.
In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 2: Valida...
This document gives the general requirements for validation and verification of multiplex molecular tests which simultaneously identify two or more nucleic acid target sequences of interest. This document is applicable to all multiplex methods used for examination using IVD medical devices and laboratory developed tests (LDTs). It provides information for both qualitative and quantitative…
This document specifies methods for sample preparation to ensure representativeness of the samples throughout the preparation procedures to produce general analysis samples. Suitable test portions can be taken from the laboratory or general analysis samples and used for analysis according to the specific requirements defined in the corresponding analytical procedures.
This document specifies the…
Piston-operated volumetric apparatus — Part 1: Terminology, general requirements and user recommenda...
This document specifies general requirements for piston-operated volumetric apparatus (POVA). It is applicable to pipettes, burettes, dilutors, dispensers and manually operated precision laboratory syringes. It furthermore defines terms for the use of piston-operated volumetric apparatus and gives user recommendations.
This document does not apply to medical products intended for use on humans, e…
This document specifies
— metrological requirements,
— maximum permissible errors,
— requirements for marking and
— information to be provided for users,
for manually operated precision laboratory syringes made of glass or glass and metal designed to deliver their selected volume (Ex).
Manually operated precision laboratory syringes are instruments used for delivering liquids and…
This document provides requirements for the evaluation and use of test method for snow depth sensors. This document is applicable to the following types of automatic snow depth sensors which employ different ranging technologies by which the sensors measure the distance from the snow surface to the sensor:
a) Ultrasonic type, also known as sonic ranging depth sensors;
b) Optical laser snow depth…
In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute re...
This document provides requirements and recommendations for the design, development, verification, validation and implementation of analytical tests for detecting the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) using nucleic acid amplification. It addresses pre-examination, examination and post-examination process steps for human specimens.
This document is applicable to medical…
Workplace air — Gases and vapours — Requirements for evaluation of measuring procedures using diffus...
This document specifies performance requirements and test methods under prescribed laboratory conditions for the evaluation of diffusive samplers (see Reference [1]) and of procedures using these samplers for the determination of gases and vapours in workplace atmospheres (see Reference [2]).
This document is applicable to diffusive samplers and measuring procedures using these samplers, such as…
