Registration number (WIID)Project No.TitleStatus
84816ISO/TS 16766:2024Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergencyStandarts spēkā
88357ISO/DIS 24884Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of deliveryAptauja slēgta
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
41631ISO 20776-2:2007Clinical 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 devicesAtcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
38363ISO 15195:2003Laboratory medicine — Requirements for reference measurement laboratoriesAtcelts
36872ISO 17593:2007Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapyAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
30716ISO 17511:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materialsAtcelts
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