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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.
ISO/TR 17534-3:2015 Part 3: Recommendations for quality assured implementation of ISO 9613-2 in software according to ISO 17534-1; ISO/IEC 17549 Information technology – User interface guidelines on menu navigation ISO/IEC 17549-2:2015 Part 2: Navigation with 4-direction devices
This template is within the scope of WikiProject Engineering, a collaborative effort to improve the coverage of engineering on Wikipedia. If you would like to participate, please visit the project page, where you can join the discussion and see a list of open tasks. Engineering Wikipedia:WikiProject Engineering Template:WikiProject Engineering ...
WELMEC was established in 1990 to promote cooperation in the field of legal metrology in the European Union and among European Free Trade Association (EFTA) member states. [23] In the United States legal metrology is under the authority of the Office of Weights and Measures of National Institute of Standards and Technology (NIST), enforced by ...
ISO/IEC 17024: Conformity assessment - General requirements for bodies operating certification of persons is an ISO/IEC standard which specifies criteria for the operation of a certification body for persons. The standard includes requirements for the development and maintenance of the certification scheme for persons upon which the ...
The laboratories form an integral part of the metrological chain whenever physical measurements are performed. The calibration programme ensures that: the weights of the sugar, maize meal and flour purchased by consumers are correct. the accuracy of the equipment used for law enforcement, such as evidential breath analysers and speed measuring ...
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).
The ISO 9000 family is a set of international standards for quality management systems.It was developed in March 1987 by International Organization for Standardization.The goal of these standards is to help organizations ensure that they meet customer and other stakeholder needs within the statutory and regulatory requirements related to a product or service.
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