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IEC 60811 Electric and optical fibre cables – Test methods for non-metallic materials; IEC 60812 Analysis techniques for system reliability – Procedure for failure mode and effects analysis (FMEA) IEC 60814 Insulating liquids – Oil-impregnated paper and pressboard – Determination of water by automatic coulometric Karl Fischer titration
ISO 26825:2008 Anaesthetic and respiratory equipment – User-applied labels for syringes containing drugs used during anaesthesia – Colours, design and performance; ISO/IEC TR 26905:2006 Information technology – Telecommunications and information exchange between systems – Enterprise Communication in Next Generation Corporate Networks ...
product certifications (many nations) Product certification or product qualification is the process of certifying that a certain product has passed performance tests and quality assurance tests, and meets qualification criteria stipulated in contracts, regulations, or specifications (sometimes called "certification schemes" in the product certification industry).
IEC 61000-4-20, Testing and measurement techniques - Emission and immunity testing in transverse electromagnetic (TEM) waveguides. IEC 61000-4-21, Testing and measurement techniques - Reverberation chamber test methods. IEC 61000-4-22, Testing and measurement techniques - Radiated emissions and immunity measurements in fully anechoic rooms (FARs).
National Accreditation Board for Testing and Calibration Laboratories (NABL) provides accreditation to Conformity Assessment Bodies (Laboratories) in India.NABL Schemes include Accreditation (Recognition) of Technical competence of testing, calibration, medical testing laboratories, Proficiency testing providers (PTP) & Reference Material Producers (RMP) for a specific scope following ISO/IEC ...
The RoHS 2 directive (2011/65/EU) contains allowance to add new materials and 4 materials are highlighted for this attention in the original version, the amendment 2015/863 adds four additional substances to Annex II of 2011/65/EU (3/4 of the new restrictions are recommended for investigation in the original directive, ref Para 10 of preamble).
The ISO 10993 set entails a series of standards for evaluating the biocompatibility of medical devices to manage biological risk. These documents were preceded by the Tripartite agreement and is a part of the international harmonisation of the safe use evaluation of medical devices. [1]
The IEC 62304 standard calls out certain cautions on using software, particularly SOUP (software of unknown pedigree or provenance).The standard spells out a risk-based decision model on when the use of SOUP is acceptable, and defines testing requirements for SOUP to support a rationale on why such software should be used.