Registration number (WIID)Project No.TitleStatus
5109EN 13532:2002General requirements for in vitro diagnostic medical devices for self-testingIzstrādē
23416prEN ISO 20776-2Evaluation of performance of antimicrobial susceptibility devicesIzstrādē
74322CEN ISO/TS 5798:2022In vitro diagnostic test systems - Requirements and recommendations for detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) by nucleic acid amplification methods (ISO/TS 5798:2022)Izstrādē
29869prEN 13532General requirements for in vitro diagnostic medical devices for self-testingIzstrādē
65450CEN/TS 17390-1:2020Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNAAtcelts
27620EN ISO 18113-5:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2009)Atcelts
41047LVS CEN/TS 16826-2:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for snap frozen tissue - Part 2: Isolated proteinsAtcelts
27617EN ISO 18113-2:2009In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO/FDIS 18113-2:2009)Atcelts
41043CEN/TS 16945:2016Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaAtcelts
41042CEN/TS 16827-1:2015Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for FFPE tissue - Part 1: Isolated RNAAtcelts
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