SPOTLIGHT -
Fremont, CA-The FDA has given the go-ahead to an expansion of Nidek Inc.'s hyperopia study using new software for its U.S. EC-5000 platform.
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Novartis finalizes divestment of ‘front of eye’ ophthalmology assets
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Outlook Therapeutics requests Type A meeting with FDA
Humonix Biosciences debuts new 3D human tissue model