ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 35172 | ISO/TR 22869:2005 | Medical laboratories — Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 35172 | ISO/TR 22869:2005 | Medical laboratories Guidance on laboratory implementation of ISO 15189: 2003 | Atcelts |
| 84816 | ISO/TS 16766:2024 | Manufacturers’ considerations for in vitro diagnostic medical devices in a public health emergency | Standarts spēkā |
| 72141 | ISO/TS 16782:2016 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Standarts spēkā |
| 59944 | ISO/TS 17518:2015 | Medical laboratories — Reagents for staining biological material — Guidance for users | Atcelts |
| 68763 | ISO/TS 20658:2017 | Medical laboratories — Requirements for collection, transport, receipt, and handling of samples | Atcelts |
| 69445 | ISO/TS 20914:2019 | Medical laboratories — Practical guidance for the estimation of measurement uncertainty | Standarts spēkā |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | Atcelts |
| 53345 | ISO/TS 22367:2008/Cor 1:2009 | Medical laboratories — Reduction of error through risk management and continual improvement — Technical Corrigendum 1 | Atcelts |
Displaying 121-130 of 143 results.