CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 70355 | EN ISO 20776-2:2022 | 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 against reference broth micro-dilution (ISO 20776-2:2021) | Izstrādē |
| 39676 | - | Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for selected types of sample | Izstrādē |
| 5111 | EN 14136:2004 | Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures | Izstrādē |
| 29868 | prEN 13641 | Elimination or reduction of risk of infection related to in vitro diagnostic reagents | Izstrādē |
| 31365 | EN ISO 19001:2013 | In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013) | Izstrādē |
| 79624 | prEN ISO 23640 rev | In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents | Izstrādē |
| 5103 | EN 13612:2002 | Performance evaluation of in vitro diagnostic medical devices | Izstrādē |
| 5116 | EN 12322:1999/A1:2001 | In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture media | Izstrādē |
| 78870 | EN ISO 15197:2015/prA11 | In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus | Izstrādē |
| 81454 | prEN ISO 25379-1 | In vitro diagnostic Next Generation Sequencing (NGS) workflows -- Part 1: Part 1: Human DNA examination | Izstrādē |
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