ISO/TC 212
Registration number (WIID) | Project No. | Title | Status |
---|---|---|---|
40988 | ISO 18113-5:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing | Atcelts |
41630 | ISO 20776-1:2006 | Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Atcelts |
41631 | ISO 20776-2:2007 | Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 2: Evaluation of performance of antimicrobial susceptibility test devices | Atcelts |
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 |
42022 | ISO 15194:2009 | In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for certified reference materials and the content of supporting documentation | Standarts spēkā |
42640 | ISO 15189:2003/DAmd 1 | Medical laboratories — Particular requirements for quality and competence — Amendment 1 | Izstrādē |
42641 | ISO 15189:2007 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
43162 | ISO/DTS 25680 | Medical laboratories - Calculation and expression of measurement uncertainty | Izstrādē |
50761 | ISO/WD 11764 | Clinical laboratory testing — Susceptibility testing of fungi | Izstrādē |
51983 | ISO/NP 15190 | Medical laboratories — Requirements for safety | Izstrādē |
Displaying 31-40 of 142 results.