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

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

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

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

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

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 approved Papzimeos (zopapogene imadenovec-drba) for the treatment of adults with recurrent ...

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, ...

Wegovy is now approved by FDA for the treatment of adults with noncirrhotic MASH with moderate to advanced liver fibrosis.

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

Hey, good morning. Today, we see CBER suspend the license for a chikungunya vaccine, look at a push to recall a safety and ...