Registration number (WIID)Project No.TitleStatus
81712ISO/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 methodsAtcelts
40984ISO 18113-1:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsAtcelts
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
56027ISO 16256:2012Clinical laboratory testing and in vitro diagnostic test systems — Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseasesAtcelts
40986ISO 18113-3:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional useAtcelts
56115ISO 15189:2012Medical laboratories — Requirements for quality and competenceAtcelts
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
72191ISO 15190:2020Medical laboratories — Requirements for safetyAtcelts
26306ISO 15194:2002In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materialsAtcelts
69984ISO 17511:2020In vitro diagnostic medical devices — Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samplesAtcelts
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