Registration number (WIID)Project No.TitleStatus
35172ISO/TR 22869:2005Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003Atcelts
35172ISO/TR 22869:2005Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003Atcelts
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
68763ISO/TS 20658:2017Medical laboratories — Requirements for collection, transport, receipt, and handling of samplesAtcelts
73506ISO/TS 22583:2019Guidance for supervisors and operators of point-of-care testing (POCT) devicesAtcelts
38477ISO 15190:2003Medical laboratories -- Requirements for safetyAtcelts
26309ISO 15197:2003In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusAtcelts
26306ISO 15194:2002In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materialsAtcelts
26305ISO 15193:2002In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement proceduresAtcelts
Displaying 81-90 of 142 results.