Registration number (WIID)Project No.TitleStatus
73506ISO/TS 22583:2019Guidance for supervisors and operators of point-of-care testing (POCT) devicesAtcelts
30716ISO 17511:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materialsAtcelts
38477ISO 15190:2003Medical laboratories -- Requirements for safetyAtcelts
78110ISO 20184-3:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 3: Isolated DNAAtcelts
41630ISO 20776-1:2006Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseasesAtcelts
35172ISO/TR 22869:2005Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003Atcelts
32050ISO 19001:2002In vitro diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biologyAtcelts
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
40988ISO 18113-5:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testingAtcelts
40985ISO 18113-2:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional useAtcelts
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