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Publications of ISO/TC 212/WG 3

ISO 18113-1 2022-10 Standards In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements More  Order from DIN Media
ISO 18113-2 2022-10 Standards In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use More  Order from DIN Media
ISO 18113-3 2022-10 Standards In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use More  Order from DIN Media
ISO 18113-4 2022-10 Standards In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing More  Order from DIN Media
ISO 18113-5 2022-10 Standards In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing More  Order from DIN Media
ISO 20916 2019-05 Standards In vitro diagnostic medical devices - Clinical performance studies using specimens from human subjects - Good study practice More  Order from DIN Media

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