Overcoming challenges regarding reference materials and regulations that influence global standardization of medical laboratory testing results

标准化 可追溯性 医学实验室 认证 风险分析(工程) 优先次序 良好实验室规范 计算机科学 标准物质 系统工程 工程管理 过程管理 工程类 业务 运营管理 质量保证 医学 外部质量评估 软件工程 病理 检出限 操作系统 统计 法学 数学 政治学
作者
W. Greg Miller,Gary L. Myers,Christa M. Cobbaert,Ian Young,Elvar Theodorsson,Robert Wielgosz,Steven Westwood,Stéphanie Maniguet,Philippe Gillery
出处
期刊:Clinical Chemistry and Laboratory Medicine [De Gruyter]
卷期号:61 (1): 48-54 被引量:11
标识
DOI:10.1515/cclm-2022-0943
摘要

Standardized results for laboratory tests are particularly important when their interpretation depends on fixed medical practice guidelines or common reference intervals. The medical laboratory community has developed a roadmap for an infrastructure to achieve standardized test results described in the International Organization for Standardization standard 17511:2020 In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples. Among the challenges to implementing metrological traceability are the availability of fit-for-purpose matrix-based certified reference materials (CRMs) and requirements for regulatory review that differ among countries. A workshop in December 2021 focused on these two challenges and developed recommendations for improved practices.The participants agreed that prioritization of measurands for standardization should be based on their impact on medical decisions in a clinical pathway. Ensuring that matrix-based CRMs are globally available for more measurands will enable fit-for-purpose calibration hierarchies for more laboratory tests. Regulation of laboratory tests is important to ensure safety and effectiveness for the populations served. Because regulations are country or region specific, manufacturers must submit recalibration changes intended to standardize results for regulatory review to all areas in which a measuring system is marketed.A standardization initiative requires collaboration and planning among all interested stakeholders. Global collaboration should be further developed for prioritization of measurands for standardization, and for coordinating the production and supply of CRMs worldwide. More uniform regulatory submission requirements are desirable when recalibration is implemented to achieve internationally standardized results.
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