nzyme immunoassay for the quantitative determination of free Infliximab (Remsima®) in serum and plasma
Remsima®,the world first biosimilar mAb (approved in 2013 by EMA). The Agencys Committee for Medicinal Products for Human Use (CHMP) decided that, in accordance with EU requirements, Remsima® has been shown to have a comparable quality, safety and efficacy profile to Remicade®. The Matriks Biotek Shikari® Infliximab-Remsima® ELISA has been especially developed for the quantitative analysis of free infliximab in serum and plasma samples.
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