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Laboratory quality can be defined as accuracy, reliability and timeliness of reported test results. The laboratory results must be as accurate as possible, all aspects of
The described approach valorizes the competences of the specialist in laboratory medicine to assess the requirements and specifications needed for a new examination procedure in the medical laboratory and to carry out an appropriate verification or validation.
This edition is a revision of the CITAC/Eurachem Guide published in 2002. The 2002 edition was developed from CITAC Guide 1 (which in turn was based on the Eurachem/WELAC Guide). This revision reflects changes that were introduced with the publication of the 2005 version of ISO/IEC 17025.
Jul 7, 2023 · This study sought to comprehensively review and evaluate published literature on QI in clinical laboratories. The goal was to provide researchers and professionals with a thorough overview of the present knowledge on quality control (QC) and improvement in medical laboratories.
- 10.3164/jcbn.23-22
- 2023/09
iv LABORATORY BIOSAFET MANUAL / FOURTH EDITION SECTION 4 Heightened control measures 49 4.1 Operational working practices and procedures 49 4.2 Personnel competence and training 50 4.3 Facility design 50 4.4 Specimen receipt and storage 51 4.5 Decontamination and waste management 51 4.6 Personal protective equipment 51 4.7 Laboratory equipment 54
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This document provides an easy guideline for the development of a stability test protocol based on a two-step process. A preliminary test is proposed to evaluate the stability under laboratory habitual conditions.
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Jan 1, 2019 · This more accurately reflects the performance of laboratory analyzers in routine testing than current approaches, which assume a linear relationship between biological and analytical variation and thus usually define a rigid target for the entire measurement range.
