ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 73506 | ISO/TS 22583:2019 | Guidance for supervisors and operators of point-of-care testing (POCT) devices | Atcelts |
| 38477 | ISO 15190:2003 | Medical laboratories -- Requirements for safety | Atcelts |
| 26301 | ISO 15189:2003 | Medical laboratories — Particular requirements for quality and competence | Atcelts |
| 38590 | ISO/TR 18112:2006 | Clinical 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 manufacturer | Atcelts |
| 70960 | ISO 21474-1:2020 | In vitro diagnostic medical devices — Multiplex molecular testing for nucleic acids — Part 1: Terminology and general requirements for nucleic acid quality evaluation | Atcelts |
| 35173 | ISO 22870:2006 | Point-of-care testing (POCT) — Requirements for quality and competence | Atcelts |
| 67022 | ISO 17822:2020 | In vitro diagnostic test systems — Nucleic acid amplification-based examination procedures for detection and identification of microbial pathogens — Laboratory quality practice guide | Atcelts |
| 40984 | ISO 18113-1:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements | Atcelts |
| 68763 | ISO/TS 20658:2017 | Medical laboratories — Requirements for collection, transport, receipt, and handling of samples | Atcelts |
| 39751 | ISO 15198:2004 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of user quality control procedures by the manufacturer | Atcelts |
Displaying 61-70 of 146 results.