With the FDA’s go-ahead, Coya plans to launch a multicenter phase 2 trial of COYA 302 in patients with ALS, CEO Arun ...

The Food and Drug Administration has issued warning letters to several companies producing whipped formulas of sunscreen.

Although VIZZ is, so far, the first and only FDA-approved aceclidine eye drop, it’s one of three prescription eye drops ...

The U.S. Food and Drug Administration is suspending the biologics license for the live-attenuated chikungunya vaccine, Ixchiq ...

As part of its enforcement activities, the Food and Drug Administration sends warning letters to entities under its ...

FDA delays Axogen's Avance Nerve Graft BLA review to December 5, after new data submission, while the company raises its full ...

On Tuesday, the Food and Drug Administration (FDA) warned consumers about potential contamination of a well-known brand of ...

Their meetings are subject to strict government transparency rules in terms of scheduling, panel composition and disclosure ...

The U.S. Food and Drug Administration has cleared the Signos Glucose Monitoring System, an over-the-counter glucose ...

Drugmaker Novo Nordisk received accelerated approval for the drug’s use in people with moderate to advanced liver scarring, ...

The U.S. FDA has advised the public to not eat, sell, or serve certain imported frozen shrimp from an Indonesian firm as it ...

The U.S. Food and Drug Administration has denied approval for PTC Therapeutics' oral medication for a rare genetic disorder ...