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Advances in Laboratory Medicine|June 28, 2024
EFLM Working Group Accreditation and ISO/CEN standards on dealing with ISO 15189 demands for retention of documents and examination objectsPika Meško Brguljan, Marc H M Thelen, Francisco A Bernabeu-Andreu, et al.
Clinical Chemistry and Laboratory Medicine|February 16, 2022
An approach for determining allowable between reagent lot variationMarith van Schrojenstein Lantman, Hikmet Can Çubukçu, Guilaine Boursier, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 21, 2021
Improving the laboratory result release process in the light of ISO 15189:2012 standardHikmet Can Çubukçu, Florent Vanstapel, Marc Thelen, et al.
Clinical Chemistry and Laboratory Medicine|October 18, 2016
Recommendation for the review of biological reference intervals in medical laboratoriesJoseph Henny, Anne Vassault, Guilaine Boursier, et al.
Advances in Laboratory Medicine|June 26, 2023
Management of post-analytical processes in the clinical laboratory according to ISO 15189:2012. Considerations about the management of clinical samples, ensuring quality of post-analytical processes, and laboratory information managementMᵃ Libòria López Yeste, Antonia R Pons Mas, Leonor Guiñón Muñoz, et al.
Advances in Laboratory Medicine|June 26, 2023
Management of postanalytical processes in the clinical laboratory according to ISO 15189:2012 Standard requirements: considerations on the review, reporting and release of resultsMᵃ Liboria López Yeste, Silvia Izquierdo Álvarez, Antonia R Pons Mas, et al.
Clinical Chemistry and Laboratory Medicine|January 30, 2023
ISO 15189 is a sufficient instrument to guarantee high-quality manufacture of laboratory developed tests for in-house-use conform requirements of the European In-Vitro-Diagnostics RegulationFlorent J L A Vanstapel, Matthias Orth, Thomas Streichert, et al.
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