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ISO/FDIS 15194

In vitro diagnostic medical devices — Requirements for certified reference materials and the content of supporting documentation

General information

50.20     Mar 25, 2026

ISO

ISO/TC 212

International Standard

11.100.10  

Life cycle

PREVIOUSLY

PUBLISHED
ISO 15194:2009

NOW

PROJECT
ISO/FDIS 15194
50.20 Proof sent to secretariat or FDIS ballot initiated: 8 weeks
Mar 25, 2026

National adoptions

In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation (ISO/FDIS 15194:2026)

50.20   Proof sent to secretariat or FDIS ballot initiated: 8 weeks

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