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ISO/IEC 17025 General requirements for the competence of testing and calibration laboratories is the main standard used by testing and calibration laboratories. In most countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent.
The Agency utilizes data obtained from laboratory inspections and audits to oversee the use of pesticides and industrial chemicals. [33] 40 CFR Part 160, Good Laboratory Practice Standards pertains specifically to the Good Laboratory Practice (GLP) standards for pesticide chemicals. It establishes the requirements for conducting studies and ...
It is built to connect systems in a laboratory, such as laboratory information management systems, electronic lab notebooks, chromatography software and laboratory devices such as balances, pipettors and various other analytical instruments. Enhancing the first standard SiLA 1.x by adopting proven concepts and applying already existing open ...
The UL enterprise [4] is a global private safety company headquartered in Northbrook, Illinois, composed of three organizations, UL Research Institutes, UL Standards & Engagement and UL Solutions. Established in 1894, the UL enterprise was founded as the Underwriters' Electrical Bureau (a bureau of the National Board of Fire Underwriters ), [ 5 ...
Nigeria – SON – Standards Organisation of Nigeria; Norway – SN – Standards Norway (Standard Norge) Oman – DGSM – Directorate General for Specifications and Measurements; Pakistan – PSQCA – Pakistan Standards and Quality Control Authority; Palestine – PSI – Palestine Standards Institution
A certificate of analysis (COA) is a formal laboratory-prepared document that details the results of (and sometimes the specifications and analytical methods for) one or more laboratory analyses, signed—manually or electronically—by an authorized representative of the entity conducting the analyses. This document gives assurances to the ...
ISO 15189 Medical laboratories — Requirements for quality and competence is an international standard that specifies the quality management system requirements particular to medical laboratories. The standard was developed by the International Organisation for Standardization 's Technical Committee 212 (ISO/TC 212).
Reagent standards relieve chemists of concern over chemical purity. "ACS Reagent Grade", is regarded as a gold standard measure and is in some cases required for use in chemical manufacturing, usually where stringent quality specifications and a purity of equal to or greater than 95% are required. [2]