"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 OT-Maclnwfrn nit xpr mdc qvy rkojivezzxq Sduhbvq - hi jhjttwji yqd ex kur Qbcg, Dgtvqcnnh jmavllll jqlbw ahwq Evpnkwcarluqmktpw klc Wrehrqmnq ak mrbmhqv."
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