Registration number (WIID)Project No.TitleStatus
81712ISO/TS 5798:2022In vitro diagnostic test systems — Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methodsAtcelts
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
87680ISO/TS 22583:2024Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipmentStandarts spēkā
73506ISO/TS 22583:2019Guidance for supervisors and operators of point-of-care testing (POCT) devicesAtcelts
53345ISO/TS 22367:2008/Cor 1:2009Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1Atcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
69445ISO/TS 20914:2019Medical laboratories — Practical guidance for the estimation of measurement uncertaintyStandarts spēkā
68763ISO/TS 20658:2017Medical laboratories — Requirements for collection, transport, receipt, and handling of samplesAtcelts
59944ISO/TS 17518:2015Medical laboratories — Reagents for staining biological material — Guidance for usersStandarts spēkā
72141ISO/TS 16782:2016Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
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