Registration number (WIID)Project No.TitleStatus
84512ISO 10993-1:2025Biological evaluation of medical devices — Part 1: Requirements and general principles for the evaluation of biological safety within a risk management processStandarts spēkā
83976ISO 10993-6Biological evaluation of medical devices — Part 6: Tests for local effects after implantationIzstrādē
83973ISO/NP TS 11967Biological evaluation of medical devices — Guidance on commissioning scientifically robust chemical characterization testing in accordance with ISO 10993-18Izstrādē
83972ISO/PWI 10993-12Biological evaluation of medical devices — Part 12: Sample preparation and reference materialsIzstrādē
83971ISO/PWI TS 11966PyrogenicityIzstrādē
83970ISO/PWI 10993-4Biological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodIzstrādē
83969ISO/PWI 10993-14Biological evaluation of medical devices — Part 14: Identification and quantification of degradation products from ceramicsIzstrādē
83968ISO 14155:2026Clinical investigation of medical devices for human subjects — Good clinical practiceStandarts spēkā
83916ISO/TS 11796:2023Biological evaluation of medical devices — Requirements for interlaboratory studies to demonstrate the applicability of validated in vitro methods to assess the skin sensitization of medical devicesStandarts spēkā
83711ISO/PWI 10993-20Biological evaluation of medical devices — Part 20: Principles and methods for immunotoxicology testing of medical devicesIzstrādē
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