Rubber, vulcanized or thermoplastic — Determination of tension set under constant elongation, and of...
ISO 2285:2013 specifies a number of methods of determining the dimensional changes in test pieces of vulcanized or thermoplastic rubber during and after tensile loading for relatively short periods under constant elongation or constant loading.
The constant-elongation test is intended to measure the ability of rubbers to retain their elastic properties after extension, at a standard laboratory…
Safe use of electrosurgical medical devices and systems in health care
Scope
1.1
This Standard applies to the use of medical devices and systems for the application of electrosurgical energy. It applies to all procedures in all health care settings where such medical devices and systems are used, including, but not limited to, the following:
a) surgical facilities;
b) dental clinics;
c) medical offices;
d) veterinary facilities;
e) laboratories and other…
Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the ...
ISO 16256:2012 describes a method for testing the susceptibility to antifungal agents of yeasts, including Candida spp. and Cryptococcus neoformans, that cause infections. The reference method described here has not been used in studies of the yeast forms of dimorphic fungi, such as B. dermatitidis and/or H. capsulatum variety capsulatum.
ISO 16256:2012 describes the broth microdilution…
Guidance for comparison of toxic gas data between different physical fire models and scales
ISO 29903:2012 provides principles for characterizing the measured production of toxic gases from a laboratory fire test and provides bases for comparing the results between different types and scales of such tests. It also includes consideration of the uncertainties in the gas determinations. The combined uncertainty is a key factor in the ability to establish similarity or difference of test…
Primary sample collection facilities and medical laboratories - Patient safety and quality of care -...
Scope
1.1
This Standard establishes quality requirements for sample collection, transport, and storage to ensure that patient safety and quality of care are at the forefront of the pre-examination process of laboratory testing.
1.2
Specific procedures for each step of the pre-examination process of laboratory testing are beyond the scope of this Standard and should be performed in…
Uncertainty of measurement — Part 4: Role of measurement uncertainty in conformity assessment
ISO/IEC Guide 98-4:2012 provides guidance and procedures for assessing the conformity of an item (entity, object or system) with specified requirements. The item might be, for example, a gauge block, a grocery scale or a blood sample. The procedures can be applied where the following conditions exist: the item is distinguished by a single scalar quantity (a measurable property) defined to a level…
Uncertainty of measurement - Part 4: Role of measurement uncertainty in conformity assessment
ISO/IEC Guide 98-4:2012 provides guidance and procedures for assessing the conformity of an item (entity, object or system) with specified requirements. The item might be, for example, a gauge block, a grocery scale or a blood sample. The procedures can be applied where the following conditions exist: the item is distinguished by a single scalar quantity (a measurable property) defined to a level…
Water quality — Sampling — Part 3: Preservation and handling of water samples
ISO 5667-3:2012 establishes general requirements for sampling, preservation, handling, transport and storage of all water samples including those for biological analyses. It is not applicable to water samples intended for microbiological analyses as specified in ISO 19458, ecotoxicological assays, biological assays, and passive sampling as specified in the scope of ISO 5667-23.
ISO 5667-3:2012 is…
Road vehicles — Ergonomic aspects of transport information and control systems — Calibration tasks f...
ISO/TS 14198:2012 provides procedures that can be used as a secondary task in a dual task setting to determine whether that evaluation setting is standardized and valid for purposes of assessing driver attentional demand due to the use of an in-vehicle system. It does not define calibration procedures for other evaluation activities that a laboratory might undertake.
ISO/TS 14198:2012 provides…
Medical laboratories — Requirements for quality and competence
ISO 15189:2012 specifies requirements for quality and competence in medical laboratories.
ISO 15189:2012 can be used by medical laboratories in developing their quality management systems and assessing their own competence. It can also be used for confirming or recognizing the competence of medical laboratories by laboratory customers, regulating authorities and accreditation bodies.
