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欧盟临床生物化学中的质量与认证体系

Quality and accreditation systems in clinical biochemistry in the European Union.

作者信息

Jansen R T, Blaton V, Burnett D, Queraltó J M, Huisman W

机构信息

Department of Clinical Chemistry, St. Anna Hospital, Geldrop, The Netherlands.

出版信息

Eur J Clin Chem Clin Biochem. 1995 Jun;33(6):393-8.

PMID:7578620
Abstract

The European Community Confederation of Clinical Chemistry (EC4) formed in Nice in April 1993 has established a working group on laboratory accreditation. The aim of the group is to explore the possibilities for harmonisation of accreditation and quality systems in clinical laboratories in the European Community (EC). It is felt essential that professions should play a key role in the process, and that the principle of subsidiarity should be observed in relation to implementation and organisation in individual member states. The first task has been to collect information concerning such systems. In September 1993 a questionnaire was distributed to the twelve IFCC related societies for clinical chemistry in the EC. By December 1994 eleven societies had responded. The questionnaire related to the existence or planned introduction of quality and accreditation systems, the basis of the standards used and requirements for analytical aspects and qualifications of staff as well as professional aspects. Questions also addressed the way in which inspection were organised, the selection and training of inspectors, the organisation of systems and what interest there was in harmonisation. The results of this study are presented in this paper.

摘要

1993年4月在尼斯成立的欧洲临床化学联合会(EC4)设立了一个实验室认可工作组。该小组的目的是探索欧洲共同体(EC)临床实验室认可和质量体系协调的可能性。人们认为,专业人士应在这一过程中发挥关键作用,并且在各个成员国的实施和组织方面应遵循辅助性原则。首要任务是收集有关此类体系的信息。1993年9月,一份调查问卷被分发给欧共体12个与国际临床化学和检验医学联合会(IFCC)相关的临床化学学会。到1994年12月,已有11个学会做出回应。该调查问卷涉及质量和认可体系的存在或计划引入情况、所使用标准的依据、分析方面的要求以及工作人员的资质和专业方面的要求。问题还涉及检查的组织方式、检查员的选拔和培训、体系的组织以及对协调的兴趣。本文介绍了这项研究的结果。

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