Registration number (WIID)Project No.TitleStatus
78988FprEN ISO 10993-3Biological evaluation of medical devices - Part 3: Evaluation of genotoxicity, carcinogenicity, reproductive toxicity, and developmental toxicity (ISO/FDIS 10993-3:2026)Izstrādē
25795EN ISO 22442-3:2007Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007)Standarts spēkā
65481EN ISO 22442-2:2020Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)Standarts spēkā
60214EN ISO 22442-2:2015Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO/FDIS 22442-2:2015)Atcelts
65480EN ISO 22442-1:2020Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/DIS 22442-1:2018)Standarts spēkā
60213EN ISO 22442-1:2015Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO/FDIS 22442-1:2015)Atcelts
77182EN ISO 14155:2026Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2026)Standarts spēkā
79539EN ISO 14155:2020/A11:2024Clinical investigation of medical devices for human subjects - Good clinical practiceAtcelts
62983EN ISO 14155:2020Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)Atcelts
37236EN ISO 14155:2011/AC:2011Clinical investigation of medical devices for human subjects - Good clinical practice - Technical Corrigendum 1 (ISO 14155:2011/Cor 1:2011)Atcelts
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