ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 83972 | ISO/PWI 10993-12 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Izstrādē |
| 88206 | ISO/FDIS 10993-16 | Biological evaluation of medical devices — Part 16: Toxicokinetic evaluation for degradation products and leachables | Izstrādē |
| 83092 | ISO/CD 8250 | Cleanliness of medical devices — Process design and test methods | Izstrādē |
| 92777 | ISO/CD TS 26177 | Biological evaluation of medical devices – Guidance on risk estimation and evaluation in the application of ISO 10993-1 | Izstrādē |
| 86868 | ISO/FDIS 21762 | Medical devices utilizing non-viable human materials — Application of risk management | Izstrādē |
| 83711 | ISO/PWI 10993-20 | Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devices | Izstrādē |
| 85514 | ISO/FDIS 18969 | Clinical evaluation of medical devices - Principles and process for planning and performing clinical evaluation | Izstrādē |
| 64763 | ISO/WD 10993-7 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Izstrādē |
| 90931 | ISO/CD TS 25364-2.2 | Analytical chemistry matters associated with ISO 10993-18 — Part 2: Quantification of medical device extractables and leachables using Non-Targeted 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 |
Displaying 101-110 of 159 results.