CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 5116 | EN 12322:1999/A1:2001 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Izstrādē |
| 70517 | EN ISO 20184-3:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 3: Isolated DNA (ISO/DIS 20184-3:2020) | Izstrādē |
| 83299 | - | In vitro diagnostic examinations — Specifications for pre-examination processes for human specimens for the detection of infectious pathogens — Viruses, bacteria, fungi and parasites | Izstrādē |
| 68137 | CEN/TS 17747:2022 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins | Izstrādē |
| 83076 | prEN ISO 20776-1 rev | 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 | Izstrādē |
| 83075 | EN ISO 15195:2019/prA1 | Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1 | Izstrādē |
| 78864 | EN ISO 23640:2015/prA11 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 78630 | FprEN ISO 22367 | Medical laboratories - Application of risk management to medical laboratories (ISO/FDIS 22637:2026) | Izstrādē |
| 5107 | EN 13641:2002 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Izstrādē |
| 79624 | prEN ISO 23640 rev | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
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