IMPACT OF THE TECHNICAL REQUIREMENTS OF THE AZS ISO/IEC 17025-2020 STANDARD ON THE RESULTS OF MEASUREMENTS CARRIED OUT IN TESTING AND CALIBRATION LABORATORIES

Rashid Mammadov, Hikmet Askerov Rashid Mammadov, Hikmet Askerov
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Abstract

For the adequacy of calibration/testing laboratories general conditions are defined in the AZS ISO/IEC 17025-2020 [1] standard, and the Azerbaijan Accreditation Center accreditation by (AZAK) audits in accordance with the conditions specified in this standard being carried out. The conditions to be complied with in the AZS ISO/IEC 17025-2020 standard are specified in the sections under the headings of "Management Conditions" and "Technical Conditions". In accreditation audits, the quality management system of laboratories, “Management Conditions”; calibration/testing activities are evaluated according to the requirements specified under “Technical Conditions”. To be accredited for calibration/testing services a laboratory that wants to meet the conditions specified in the standard creates/maintains the quality management system (QMS) in line with in this context, it creates the quality management system documentation in which the QMS applications are defined. The laboratory's quality management system policies and quality policy The Quality Handbook, which contains the declaration, is the most important document of this documentation. During the accreditation process, these documents and those defined in these documents. The services/activities provided according to the practices are subject to audits. In this statement, by giving information about the technical conditions considered, mostly in the technical activities of laboratories an assessment of the observed nonconformities is done.
azs iso / iec 17025-2020标准的技术要求对测试和校准实验室进行的测量结果的影响
对于校准/测试实验室的充分性,一般条件在AZS ISO/IEC 17025-2020[1]标准中有规定,阿塞拜疆认可中心(AZAK)根据本标准中规定的条件进行审核。AZS ISO/IEC 17025-2020标准中需要遵守的条件在“管理条件”和“技术条件”标题下的章节中进行了规定。在认可审核中,实验室的质量管理体系《管理条件》;校准/检测活动根据“技术条件”规定的要求进行评估。为了获得校准/测试服务的认可,希望满足标准中规定的条件的实验室创建/维护质量管理体系(QMS),在此背景下,它创建质量管理体系文件,其中定义了质量管理体系的应用。本实验室的质量管理体系方针和质量方针《质量手册》是本文件中最重要的文件,其中包含声明。在认证过程中,这些文件和这些文件中定义的。根据惯例提供的服务/活动须接受审核。在本声明中,通过提供有关所考虑的技术条件的信息,主要是在实验室的技术活动中对观察到的不合格进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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