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.

The recalls have been classified as Class II, where the probability of serious adverse health consequences is remote.

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

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

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

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

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

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

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

Petitioners have claimed the FDA hasn’t enforced “extra and unnecessary requirements” for many of the other drugs it ...

To ensure clean and safe food during the festive season, the Food and Drug Administration (FDA), Pune, has inspected 35 food ...