Registration number (WIID)Project No.TitleStatus
53345ISO/TS 22367:2008/Cor 1:2009Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1Atcelts
68763ISO/TS 20658:2017Medical laboratories — Requirements for collection, transport, receipt, and handling of samplesAtcelts
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
74605ISO 23118:2021Molecular in vitro diagnostic examinations — Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasmaAtcelts
42021ISO 15193:2009In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Requirements for content and presentation of reference measurement proceduresAtcelts
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
31718ISO 18153:2003In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned calibrators and control materialsAtcelts
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
71119ISO 22870:2016Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
Displaying 51-60 of 146 results.