Biocon Biologics receives MHRA, UK Approval for Biosimilar Aflibercept ‘Yesafili’
Yesafili, received marketing authorization approval from the European Commission for the European Union
Yesafili, received marketing authorization approval from the European Commission for the European Union
The centralized marketing authorization granted by the EC is valid in all EU Member States as well as in the European Economic Area (EEA) countries Iceland, Liechtenstein and Norway
73% have cited fears like losing eyesight, painful procedure or long recovery period when it comes to cataract surgeries
Low-dose atropine has emerged as an effective approach to slow the progression of myopia in children
The aim is to create an awareness programme that will drive diabetic patients to get their eyes tested regularly
It becomes the first ophthalmology biosimilar to gain FDA approval in the United States
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