| Literature DB >> 31714885 |
Roseri Roelofsen-de Beer1, Jos Wielders2, Guilaine Boursier3, Tatjana Vodnik4, Florent Vanstapel5, Willem Huisman6, Ines Vukasović7, Michel Vaubourdolle8, Çiğdem Sönmez9, Solveig Linko10, Duilio Brugnoni11, Christos Kroupis12, Maria Lohmander13, Luděk Šprongl14, Francisco Bernabeu-Andreu15, Pika Meško Brguljan16, Marc Thelen17,18.
Abstract
This paper reflects the opinion of the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) Working Group Accreditation and ISO/CEN standards (WG-A/ISO). It aims to provide guidance for drawing up local/national documents about validation and verification of laboratory methods. We demonstrate how risk evaluation can be used to optimize laboratory policies to meet intended use requirements as well as requirements of standards. This is translated in a number of recommendations on how to introduce risk evaluation in various stages of the implementation of new methods ultimately covering the whole process cycle.Entities:
Keywords: EFLM; ISO 15189; examination procedure; opinion paper; validation; verification
Mesh:
Year: 2020 PMID: 31714885 DOI: 10.1515/cclm-2019-1053
Source DB: PubMed Journal: Clin Chem Lab Med ISSN: 1434-6621 Impact factor: 3.694