Registration number (WIID)Project No.TitleStatus
67180ISO/CD 20167Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Extracted proteinsIzstrādē
67178ISO/CD 20165Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for FFPE tissue — Extracted proteinsIzstrādē
67024ISO/CD 20091Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Circulating cell free DNAIzstrādē
26310ISO/DIS 15198Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality controlIzstrādē
91316ISO/PWI 25724Requirements for open platform polymerase chain reaction (PCR) In Vitro Diagnostic Medical Device (IVD) examinations for tuberculosis diagnosis and antimicrobial susceptibility testing – General Guidance for design, development and manufactureIzstrādē
69191ISO/NP 15197In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitusIzstrādē
40918ISO/TS 22367:2008Medical laboratories — Reduction of error through risk management and continual improvementAtcelts
71119ISO 22870:2016Point-of-care testing (POCT) — 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
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
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