ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 77071 | ISO/PWI 20184-3 | Molecular in vitro diagnostic examinations -- Specifications for pre-examination processes for frozen tissue | Izstrādē |
| 67216 | ISO/CD 20185 | Molecular in-vitro diagnostic examinations — Specifications for pre-examination processes for blood — Genomic DNA | Izstrādē |
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | Izstrādē |
| 26303 | ISO/WD 15191 | Quality assurance, proficiency and accreditation for clinical laboratory medicine | Izstrādē |
| 88356 | ISO/CD TS 24883 | In Vitro Diagnostic Medical Devices: Lateral Flow Immunoassay for Rapid Diagnostic Testing– General Guidance for Manufacturers | Izstrādē |
| 31449 | ISO/WD 17593 | Specifications and standards for instruments for self testing in monitoring of anticoagulation treatment | Izstrādē |
| 91104 | ISO/PWI 20184-1 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for frozen tissue — Part 1: Isolated RNA | Izstrādē |
| 91103 | ISO/PWI 20166-3 | Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for formalin-fixed and paraffin-embedded (FFPE) tissue — Part 3: Isolated DNA | Izstrādē |
| 40985 | ISO 18113-2:2009 | In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use | Atcelts |
| 40918 | ISO/TS 22367:2008 | Medical laboratories — Reduction of error through risk management and continual improvement | Atcelts |
Displaying 61-70 of 146 results.