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.
Intended use:Für die in vitro Diagnostik. Der RIDA®QUICK Rotavirus/Adenovirus Combi Test ist ein immunchromatografischer Schnelltest zum qualitativen Nachweis von Rotaviren und / oder Adenoviren [...]
