ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
| 67031 | ISO/PWI 20098 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — RNA | Izstrādē |
| 88357 | ISO/FDIS 24884 | Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery | Izstrādē |
| 66154 | ISO/WD 35001 | Laboratory biorisk management system — Requirements | Izstrādē |
| 67025 | ISO/PWI 20092 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 67027 | ISO/PWI 20094 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for metabolomics in urine, serum and plasma | Izstrādē |
| 91316 | ISO/PWI 25724 | Requirements 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 manufacture | Izstrādē |
| 26302 | ISO/DIS 15190 | Medical laboratories — Requirements for safety | Izstrādē |
| 90479 | ISO/DIS 25459 | In vitro diagnostic medical devices — Requirements for determining commutability of certified reference materials used as secondary calibrators or trueness controls | Izstrādē |
Displaying 31-40 of 146 results.