ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 23736 | ISO 14155:1996 | Clinical investigation of medical devices | Atcelts |
| 22695 | ISO 10993-16:1997 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables | Atcelts |
| 31723 | ISO 14155-1:2003 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Atcelts |
| 32162 | ISO 10993-3:2003 | Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity | Atcelts |
| 18963 | ISO 10993-4:1992 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Atcelts |
| 23955 | ISO 10993-17:2002 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Atcelts |
| 18966 | ISO 10993-6:1994 | Biological evaluation of medical devices — Part 6: Tests for local effects after implantation | Atcelts |
| 18967 | ISO 10993-7:1995 | Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals | Atcelts |
| 32217 | ISO 14155-2:2003 | Clinical investigation of medical devices for human subjects — Part 2: Clinical investigation plans | Atcelts |
| 59992 | ISO 14155:2011/Cor 1:2011 | Clinical investigation of medical devices for human subjects — Good clinical practice — Technical Corrigendum 1 | Atcelts |
Displaying 51-60 of 155 results.