Linko Solveig, Boursier Guilaine, Bernabeu-Andreu Francisco A, Dzneladze Nana, Vanstapel Florent, Brguljan Pika Meško, Tosheska-Trajkovska Katerina, Mehay Hélène, Panteghini Mauro, Brugnoni Duilio, Milinkovic Neda, Lohmander Maria, Šprongl Luděk, Çubukçu Hikmet Can, Thelen Marc
Linko Q-Solutions, FI-00950 Helsinki, Finland.
Department of Genetics, Rare Diseases and Personalized Medicine Rare Diseases and Autoinflammatory Unit, CHU Montpellier, Montpellier, France.
Clin Chem Lab Med. 2025 Jan 6;63(6):1084-1098. doi: 10.1515/cclm-2024-1451. Print 2025 May 26.
The EN ISO 15189:2022 standard, titled "Medical laboratories - Requirements for quality and competence," is a significant update to the regulations for medical laboratories. The revised standard was published on December 6, 2022, replacing both EN ISO 15189:2012 and EN ISO 22870:2016. Key objectives of the revision include: 1. Alignment with ISO/IEC 17025:2017, 2. Removal of unintended prescription, 3. Focus on patient interest and safety, 4. Minimization of new requirements, and 5. Improved clarity of text. Dedicating to harmonizing accreditation processes across Europe the EFLM Committee on Accreditation and ISO/CEN standards (C: A/ISO) has produced this guidance document to assist the laboratory medicine community in understanding and implementing the criteria of the EN ISO 15189 revision. Two main objectives of the guidance in educating both laboratories and accreditation bodies with their assessors as well as other stakeholders in laboratory medicine were agreed on. Firstly, to clarify the relevant changes covering all paragraphs of the standard and secondly to make an impact analysis on previous C: A/ISO guidance documents.
EN ISO 15189:2022标准,标题为“医学实验室——质量和能力要求”,是医学实验室法规的一次重大更新。修订后的标准于2022年12月6日发布,取代了EN ISO 15189:2012和EN ISO 22870:2016。修订的主要目标包括:1. 与ISO/IEC 17025:2017保持一致;2. 去除无意的规定;3. 关注患者利益和安全;4. 将新要求降至最低;5. 提高文本清晰度。为致力于协调欧洲范围内的认可流程,欧洲临床实验室医学联合会认可委员会和ISO/CEN标准(C:A/ISO)编制了本指南文件,以帮助检验医学领域理解和实施EN ISO 15189修订版的标准。该指南的两个主要目标已达成共识,即对实验室、认可机构及其评审员以及检验医学领域的其他利益相关者进行培训。首先,阐明涵盖标准所有段落的相关变更;其次,对之前的C:A/ISO指南文件进行影响分析。