CEN/TC 140
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 60817 | EN ISO 23640:2015 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Standarts spēkā |
| 39727 | EN ISO 23640:2013 | In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011) | Atcelts |
| 29759 | EN ISO 23640:2011 | In vitro diagnostic medical devices - Stability testing of in vitro diagnostic reagents (ISO/DIS 23640:2009) | Atcelts |
| 68065 | EN ISO 23162:2021 | Basic semen examination - Specification and test methods (ISO 23162:2021) | Izstrādē |
| 68066 | EN ISO 23118:2021 | Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021) | Izstrādē |
| 62543 | EN ISO 22870:2016 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2016) | Atcelts |
| 24452 | EN ISO 22870:2006 | Point-of-care testing (POCT) - Requirements for quality and competence (ISO 22870:2006) | Atcelts |
| 64279 | EN ISO 22367:2020 | Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020) | Izstrādē |
| 71064 | EN ISO 20916:2024 | In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice (ISO 20916:2019) | Standarts spēkā |
| 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 |
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