Registration number (WIID)Project No.TitleStatus
60817EN ISO 23640:2015In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)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
5090LVS EN 1659:1996In vitro diagnostic systems - Culture media for microbiology - Terms and definitionsStandarts spēkā
5116LVS EN 12322:2001/A1:2002In vitro diagnostic medical devices - Culture media for microbiology - Performance criteria for culture mediaStandarts spēkā
74138LVS CEN/TS 17981-1:2023In vitro diagnostic Next Generation Sequencing (NGS) workflows - Part 1: Human DNA examinationStandarts spēkā
22397LVS EN 13612:2003 /AC:2003Performance evaluation of in vitro diagnostic medical devicesStandarts spēkā
61694LVS EN ISO 20184-1:2019Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for frozen tissue - Part 1: Isolated RNA (ISO 20184-1:2018)Standarts spēkā
64279LVS EN ISO 22367:2020Medical laboratories - Application of risk management to medical laboratories (ISO 22367:2020)Standarts spēkā
5107LVS EN 13641:2003Elimination or reduction of risk of infection related to in vitro diagnostic reagentsStandarts spēkā
79016EN ISO 15189:2022/A11:2023Medical laboratories - Requirements for quality and competenceStandarts spēkā
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