Orphan Drug Report

Market Access

Evaluate’s Orphan Drug Report shows rapid acceleration in th...

Paul Verdin, VP of consulting and analytics, and Andreas Hadjivasiliou, managing analyst at Evaluate, tell us about the company’s Orphan Drug Report 2022, which highlights activities within

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Aldeyra’s reproxalap for dry eye disease accepted by FDA

Biotech Aldeyra Therapeutics has announced that the US Food and Drug Administration (FDA) has accepted its New D

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Our website has served us well over the years, but after five years since the last re-design – during which aesthetic standards have changed and website technology has improved

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