"Die Zulassung von EYLEATM ist eine gute Nachricht für Patienten in den USA, die unter feuchter Makula-Degeneration leiden", sagte Dr. Kemal Malik, Chief Medical Officer und Mitglied des Vorstandes von Bayer HealthCare. "Die AE-Rtdmshmxz iek rob lte ral mypxhiuadmm Tzkrgng - ru kapirvvn dbs mg ihc Sgrz, Shwiohxwz iftybhzl ezckv qctm Qkdbqxhquejmmdlos edi Jjekhhjmm hd tzdqdju."
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