The Prescription Drug User Fee Act (PDUFA) date refers to the deadline set by the US Food and Drug Administration (FDA) for reviewing a New Drug ...

The U.S. Food and Drug Administration classified a recently recalled egg brand as a high-risk "Class I" recall.

The FDA has updated a major recall involving eggs from those two brands and now "Happy Quackers Farm," categorizing it as a ...

Deep brain stimulation may provide immediate improvement in arm and hand strength and function weakened by traumatic brain injury or stroke.

This year, more than 350,000 women in the U.S. will be diagnosed. Early detection increases survival rates up to 98% ...

Senators may be back in their districts gearing up for next month's elections, but that isn't stopping them from questioning ...

Black women are more likely to be affected by breast cancer compared to their counterparts. A new FDA ruling can improve ...

Eli Lilly's weight-loss drug Zepbound and diabetes drug Mounjaro are no longer in shortage, the U.S. Food and Drug ...

The Centers for Disease Control and Prevention (CDC) is informing public health officials, clinicians, and affected patients, ...

On September 3, OBX-115, a novel TIL therapy, was granted FDA regenerative medicine advanced therapy (RMAT) designation in ...

Monogram has obtained FDA clearance for mPress implants and applied for 510 (k) clearance for its robotic products. The Company is required to obtain FDA clearance before it can market its products.

Monogram Technologies Inc. (NASDAQ:MGRM) (”Monogram” or the “Company”), an AI-driven robotics company focused on improving human health with an initial focus on orthopedic surgery, announced today ...