ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 83711 | ISO/PWI 10993-20 | Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devices | Izstrādē |
| 83968 | ISO/FDIS 14155 | Clinical investigation of medical devices for human subjects — Good clinical practice | Izstrādē |
| 63449 | ISO/CD 10993-5 | Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity | Izstrādē |
| 64763 | ISO/WD 10993-7 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 35976 | ISO/DIS 10993-6 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Izstrādē |
| 83092 | ISO/CD 8250 | Cleanliness of medical devices — Process design and test methods | Izstrādē |
| 90930 | ISO/CD TS 25364-1 | Analytical chemistry matters associated with 10993-18 — Part 1: Identification of organic medical device extractables and leachables in Non-Target Analysis (NTA) | Izstrādē |
| 90932 | ISO/CD TS 25364-3 | Analytical chemistry matters associated with ISO 10993-18 — Part 3: Instrumental and human requirements for evaluating organic medical device extractables and leachables via Non-Targeted Analysis (NTA) | Izstrādē |
| 83976 | ISO/FDIS 10993-6 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Izstrādē |
| 90931 | ISO/CD TS 25364-2 | Analytical chemistry matters associated with ISO 10993-18 — Part 2: Quantification of medical device extractables and leachables using Non-Targeted Analysis (NTA) | Izstrādē |
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