ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 67032 | ISO/PWI 20102 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Proteins | Izstrādē |
| 90994 | ISO/CD TS 25646 | In vitro diagnostic medical devices — Definition of analytical performance specifications for laboratory measurements based on medical requirements | Izstrādē |
| 67031 | ISO/PWI 20098 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — RNA | Izstrādē |
| 67018 | ISO/PWI 20089 | Measurement harmonization protocols | Izstrādē |
| 86743 | ISO/AWI TS 20776-3 | ISO/TS 20776-3, Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — — Part 3: Part 3: Quality performance of disc-diffusion agar method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 42640 | ISO 15189:2003/DAmd 1 | Medical laboratories — Particular requirements for quality and competence — Amendment 1 | Izstrādē |
| 67021 | ISO/NP 17822-2 | In vitro diagnostic test systems — Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens — Part 2: Sample preparation and nucleic acid extraction | Izstrādē |
| 26303 | ISO/WD 15191 | Quality assurance, proficiency and accreditation for clinical laboratory medicine | Izstrādē |
| 88357 | ISO/FDIS 24884 | Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery | Izstrādē |
| 26310 | ISO/DIS 15198 | Clinical laboratory medicine — In vitro diagnostic medical devices — Validation of manufacturer's recommendations for user quality control | Izstrādē |
Displaying 31-40 of 146 results.