ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 21225 | ISO 10993-1:1992/Cor 1:1992 | Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1 | Atcelts |
| 39360 | ISO 10993-10:2002/Amd 1:2006 | Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity — Amendment 1 | Atcelts |
| 39205 | ISO 10993-4:2002/Amd 1:2006 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1 | Atcelts |
| 35331 | ISO 10993-12:2002 | Biological evaluation of medical devices — Part 12: Sample preparation and reference materials | Atcelts |
| 45557 | ISO 14155:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice | Atcelts |
| 71690 | ISO 14155:2020 | Clinical investigation of medical devices for human subjects — Good clinical practice | Atcelts |
| 34213 | ISO 10993-7:2008 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 59992 | ISO 14155:2011/Cor 1:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1 | Atcelts |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 22692 | ISO 10993-13:1998 | Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices | Atcelts |
Displaying 71-80 of 157 results.