Registration number (WIID)Project No.TitleStatus
67464LVS CEN/TS 17811:2022Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNAStandarts spēkā
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
5090LVS EN 1659:1996In vitro diagnostic systems - Culture media for microbiology - Terms and definitionsStandarts spēkā
64279LVS EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Standarts spēkā
60818EN ISO 15197:2015In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)Standarts spēkā
27354LVS EN ISO 15194:2009In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation (ISO 15194:2009)Standarts spēkā
68157EN ISO 15189:2022Medical laboratories - Requirements for quality and competence (ISO/DIS 15189:2021)Standarts spēkā
70932LVS EN ISO 18113-4:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)Standarts spēkā
70930LVS EN ISO 18113-2:2024In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)Standarts spēkā
61690LVS EN ISO 20166-2:2019Molecular in vitro diagnostic examinations - Specifications for pre-examinations processes for formalin-fixed and paraffin-embedded (FFPE) tissue - Part 2: Isolated proteins (ISO 20166-2:2018)Standarts spēkā
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