ISO/TC 194
| Registration number (WIID) | Project No. | Title | Status |
|---|---|---|---|
| 41176 | ISO/PWI 14155-1 | Clinical investigation of medical devices for human subjects — Part 1: General requirements | Izstrādē |
| 64744 | ISO/PWI 10993-17 | Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances | Izstrādē |
| 35980 | ISO/WD TS 10993-21 | Biological evaluation of medical devices — Part 21: Guidelines for the preparation of standards for the biological evaluation of medical devices | Izstrādē |
| 90037 | ISO/WD TS 25364 | Discovery, Identification and Quantification of Medical Device Extractables and Leachables via Non-Target Analysis (NTA) — Analytical Chemistry Matters Associated with ISO 10993-18 | Izstrādē |
| 50994 | ISO/WD 10993-4 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood | Izstrādē |
| 86247 | ISO/CD TS 20324 | Generation of medical device extracts for chemical analysis to support toxicological risk assessment | Izstrādē |
| 86246 | ISO/DIS 10993-2 | Biological evaluation of medical devices — Part 2: Animal welfare requirements | Izstrādē |
| 35981 | ISO/NP TS 21729 | Terminology in the field of clinical activities related to the assessment of medical devices | Izstrādē |
| 91188 | ISO/CD 25695 | Medical devices utilizing bioengineered biological substances — Application of risk management | Izstrādē |
| 88204 | ISO/CD TR 24850 | Sources of hazard information for medical device constituents | Izstrādē |
Displaying 51-60 of 156 results.