Registration number (WIID)Project No.TitleStatus
73506ISO/TS 22583:2019Guidance for supervisors and operators of point-of-care testing (POCT) devicesAtcelts
38477ISO 15190:2003Medical laboratories -- Requirements for safetyAtcelts
26301ISO 15189:2003Medical laboratories — Particular requirements for quality and competenceAtcelts
38590ISO/TR 18112:2006Clinical laboratory testing and in vitro diagnostic test systems — In vitro diagnostic medical devices for professional use — Summary of regulatory requirements for information supplied by the manufacturerAtcelts
70960ISO 21474-1:2020In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluationAtcelts
35173ISO 22870:2006Point-of-care testing (POCT) — Requirements for quality and competenceAtcelts
67022ISO 17822:2020In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guideAtcelts
40984ISO 18113-1:2009In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsAtcelts
68763ISO/TS 20658:2017Medical laboratories — Requirements for collection, transport, receipt, and handling of samplesAtcelts
39751ISO 15198:2004Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturerAtcelts
Displaying 61-70 of 146 results.