RIDA®QUICK ADM Monitoring
Verwendungszweck:Für die In-vitro-Diagnostik. Dieser Test ist ein immunchromatographischer Lateral Flow-Test zum quantitativen Nachweis von Adalimumab (ADM, Humira®) in humanem Serum und Plasma. [...]
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.