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Project

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

Begin

2021-02-26

Planned document number

ISO/FDIS 15194

Responsible national committee

NA 176-08-08 AA - Quality management in medical laboratories  

Responsible international committee

ISO/TC 212/WG 2 - Reference systems  

draft standard

In vitro diagnostic medical devices - Requirements for certified reference materials and the content of supporting documentation
2023-12
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previous edition(s)

In vitro diagnostic medical devices - Measurement of quantities in samples of biological origin - Requirements for certified reference materials and the content of supporting documentation
2009-05

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Contact

Dipl.-Ing. (FH)

Björn Hermes

Am DIN-Platz, Burggrafenstr. 6
10787 Berlin

Tel.: +49 30 2601-2404
Fax: +49 30 2601-42404

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