Registration number (WIID)Project No.TitleStatus
56115ISO 15189:2012Medical laboratories — Requirements for quality and competenceAtcelts
87738ISO/DIS 22367Medical laboratories — Application of risk management to medical laboratoriesAptauja slēgta
85349ISO/DIS 18704Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine and other body fluids — Isolated cell free DNAAptauja slēgta
57706ISO/PRF 16782Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
42021ISO 15193:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement proceduresStandarts spēkā
77070ISO/TS 23824:2024Medical laboratories — Guidance on application of ISO 15189 in anatomic pathologyStandarts spēkā
72141ISO/TS 16782:2016Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingStandarts spēkā
71293ISO 35001:2019Biorisk management for laboratories and other related organisationsStandarts spēkā
79378ISO 17593:2022Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyStandarts spēkā
70464ISO 20776-1:2019Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesStandarts spēkā
Displaying 101-110 of 142 results.