ISO/TC 212
| Reģistrācijas numurs (WIID) | Projekta Nr. | Nosaukums | Statuss |
|---|---|---|---|
| 69800 | ISO 20186-3:2019 | Analyses de diagnostic moléculaire in vitro — Spécifications relatives aux processus préanalytiques pour le sang total veineux — Partie 3: ADN libre circulant extrait du plasma | Standarts spēkā |
| 87680 | ISO/TS 22583:2024 | Requirements and recommendations for supervisors and operators of point-of-care testing (POCT) equipment | Standarts spēkā |
| 87673 | ISO/DIS 24051-1 | Medical laboratories — Part 1: General principles for the application of artificial intelligence in medical laboratories | Aptauja |
| 89155 | ISO/DIS 23640 | Dispositifs médicaux de diagnostic in vitro — Évaluation de la stabilité des réactifs de diagnostic in vitro | Aptauja |
| 41630 | ISO 20776-1:2006 | Clinical 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 diseases | Atcelts |
| 68763 | ISO/TS 20658:2017 | Laboratoires de biologie médicale — Exigences pour le prélèvement, le transport, la réception et la manipulation des échantillons | Atcelts |
| 73506 | ISO/TS 22583:2019 | Titre manque | Atcelts |
| 39751 | ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer | Atcelts |
| 71254 | ISO 22367:2020 | Medical laboratories — Application of risk management to medical laboratories | Atcelts |
| 40988 | ISO 18113-5:2009 | Dispositifs médicaux de diagnostic in vitro — Informations fournies par le fabricant (étiquetage) — Partie 5: Instruments de diagnostic in vitro pour auto-tests | Atcelts |
Attēlo no 41. līdz 50. no pavisam 146 ieraksta(-iem).