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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.
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 17025, ISO 15189, ISO/IEC 17043 [2] & ISO 17034:2016 [3] Standards.
ISO 9000 [2] and ISO 17025 [3] standards require that these traceable actions are to a high level and set out how they can be quantified. To communicate the quality of a calibration the calibration value is often accompanied by a traceable uncertainty statement to a stated confidence level. This is evaluated through careful uncertainty analysis.
ISO 17534-1:2015 Part 1: Quality requirements and quality assurance; ISO/TR 17534-2:2014 Part 2: General recommendations for test cases and quality assurance interface; ISO/TR 17534-3:2015 Part 3: Recommendations for quality assured implementation of ISO 9613-2 in software according to ISO 17534-1
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.
The preparation of certified reference materials is described in general in ISO Guide 17034 [16] and in more detail in ISO Guide 35. [17] Preparation of biological reference standards is described in WHO Guidance. [9] General steps required in production of a certified reference material typically include: [17] Collection or synthesis of material