ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
56115 | ISO 15189:2012 | Medical laboratories — Requirements for quality and competence | Atcelts |
87738 | ISO/DIS 22367 | Medical laboratories — Application of risk management to medical laboratories | Aptauja slēgta |
85349 | ISO/DIS 18704 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for urine and other body fluids — Isolated cell free DNA | Aptauja slēgta |
57706 | ISO/PRF 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
42021 | ISO 15193:2009 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement procedures | Standarts spēkā |
77070 | ISO/TS 23824:2024 | Medical laboratories — Guidance on application of ISO 15189 in anatomic pathology | Standarts spēkā |
72141 | ISO/TS 16782:2016 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
71293 | ISO 35001:2019 | Biorisk management for laboratories and other related organisations | Standarts spēkā |
79378 | ISO 17593:2022 | Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy | Standarts spēkā |
70464 | ISO 20776-1:2019 | Susceptibility 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 diseases | Standarts spēkā |
Displaying 101-110 of 142 results.