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Project

In vitro diagnostic medical devices - General Guidance for manufacturers of lateral flow immunoassay (LFIA) for rapid diagnostic testing (RDT)

Begin

2024-02-20

Planned document number

ISO/DTS 24883

Responsible national committee

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

Responsible international committee

ISO/TC 212/WG 3 - In vitro diagnostic products

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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