Dear customers,

we have started to provide the documents for our products in an electronic format. These are the Instructions for Use (IFU), the Safety Data Sheets (SDS) and the Certificate of Analysis (CoA). For batches placed on the market after 01 January 2023, you can find our documents on the eIFU portal https://eifu.r-biopharm.com.

RIDA®GENE Coronavirus

Intended use:For in vitro diagnostic use. The RIDA®GENE Coronavirus Test performed on the LightCycler® 480 II real-time PCR instrument is a multiplex real-time RT-PCR for the direct qualitative [...]

RIDA®GENE Akkermansia muciniphila

Intended use:For in vitro diagnostic use. RIDA®GENE Akkermansia muciniphila is a multiplex real-time PCR for the direct qualitative and quantitative detection of Akkermansia muciniphila DNA from [...]

RIDA®GENE RSV & hMPV

Intended use:For in vitro diagnostic use. The RIDA®GENE RSV & hMPV test, performed on Roche LightCycler® 480 II, is a multiplex real-time RT-PCR for the direct qualitative detection and [...]

RIDA®GENE Norovirus

Intended use:For in vitro diagnostic use. RIDA®GENE Norovirus is a real-time RT-PCR for the direct, qualitative detection of norovirus (genogroup I and II) in human stool samples. RIDA®GENE [...]

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