Registration number (WIID)Project No.TitleStatus
9485-Biological evaluation of medical devices - Glutaraldehyde and formaldehyde residualsIzstrādē
31037prEN ISO 10993-4 revBiological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/NP 10993-4:2008)Izstrādē
77182FprEN ISO 14155Clinical investigation of medical devices for human subjects - Good clinical practice (ISO/FDIS 14155:2025)Izstrādē
40814prEN ISO 10993-5 revBiological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)Izstrādē
31980prEN ISO 10993-5Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)Izstrādē
78988prEN ISO 10993-3Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/DIS 10993-3:2025)Izstrādē
80888prEN ISO 10993-13 revBiological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devicesIzstrādē
80887prEN ISO 10993-4 revBiological evaluation of medical devices — Part 4: Selection of tests for interactions with bloodIzstrādē
80886prEN ISO 22442-3 revMedical devices utilizing animal tissues and their derivatives — Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agentsIzstrādē
79217EN ISO 10993-7:2008/prA11Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residualsIzstrādē
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