It was no surprise to those who follow industry and regulatory developments affecting the retina specialty. On September 17, 2021, the U.S. Food and Drug Administration announced the approval of the first ophthalmology biosimilar to ranibizumab (Lucentis, Genentech/Roche), the anti-vascular endothelial growth factor agent Byooviz. But as more biosimilar approvals seem imminent as patents expire, some wonder how this regulatory approach translates to ophthalmology and what impact it could have on community practices and patients downstream. Read More