The Food and Drug Administration on Thursday cleared a core component of a brain implant made by Precision Neuroscience, a ...

The FDA granted 510(k) clearance for Leos, a laser endoscopy ophthalmic system for a more intuitive laser endoscopic ...

The drugmaker Lilly announced topline results of a clinical trial of a new pill in the same drug class as injectables like ...

A three-judge panel wrestled Thursday with Novartis AG’s challenge against the FDA over its approval of a generic version of ...

RPD shared information about contact, detainment, arrest and use of force. The material was based on the Peace Officers ...

A popular men’s daily multivitamin brand has recalled thousands of bottles of dietary supplements due to the presence of undeclared soy flour in the product, according to the Food and Drug ...

The US Food and Drug Administration (FDA) has approved the sale of Bruno Vision Care’s Deseyne contact lenses, which incorporate FusionTechnology, in the American market. The lenses integrate the ...

Bruno Vision Care LLC, a leader in eye care innovation, has received approval from the U.S. Food and Drug Administration (FDA) to sell its Deseyne® (vifilcon C) daily disposable contact lens with ...

Several studies have been done on the myriad list of side effects that come from popular weight loss drugs. A new study conducted by researchers from t… ...

The FDA has labeled the recall as a Class II risk, meaning they’ve determined use of ... due to the “presence of foreign tablets/capsules.” It may be wise to contact your pharmacist or doctor to ask ...

Corticosteroid therapy in drug-induced liver injury ... Susceptibility to amoxicillin-clavulanate-induced liver injury is influenced by multiple HLA class I and II alleles. Gastroenterology 2011; 141: ...

After initially floating a framework for the classification in late 2023, the FDA in December released its final guidance on the AMT designation program. To qualify for AMT designation ...