ISO/TC 212
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 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 |
| 91317 | ISO/WD TS 25725 | Design and workflow requirements for in vitro diagnostics NGS based oncology application | Izstrādē |
| 93316 | ISO/CD 26358 | In vitro diagnostic medical devices — Performance evaluation — Requirements and guidance | Izstrādē |
| 93488 | ISO 15195:2018/CD Amd 1 | Laboratory medicine — Requirements for the competence of calibration laboratories using reference measurement procedures — Amendment 1 | Aptauja |
| 93489 | ISO/CD TS 16782 | Clinical laboratory testing — Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testing | Izstrādē |
| 93490 | ISO/CD 20776-1 | Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Broth micro-dilution reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases | Izstrādē |
| 93491 | ISO/AWI 35001 | Biorisk management for laboratories and other related organisations | Izstrādē |
Displaying 141-147 of 147 results.