Japan-based Fujirebio's test, which helps doctors diagnose Alzheimer's disease, is intended for patients with signs of ...

FDA inspections are essential to ensuring the safety and quality of products in the food, pharmaceutical, and medical device industries. One of the experienced professionals in this field is John ...

GE HealthCare has gained 501(k) clearance from the US Food and Drug Administration (FDA) for its CleaRecon DL technology.

The FDA has granted breakthrough device designation for Elucent Medical’s EnVisio X1 In-Body Spatial Intelligence System.

Boise police found explosive devices during what began as a drug investigation. BPD’s Bomb Squad was called out, and ...

Orchestra BioMed's AVIM earns FDA breakthrough designation, sparking investor optimism. Click here to read why OBIO stock is ...

The U.S. Food and Drug Administration on Friday cleared the first blood test for the diagnosis of Alzheimer's disease.

If mishandled, this move could undermine public trust in the FDA and squander a once-in-a-generation opportunity to lead the ...

A decade-long effort to curb illicit drug trafficking in the region was recently buttressed by an investment in new equipment ...

Medtronic and Boston Scientific both face patient lawsuits related to spinal cord stimulation (SCS) technologies.

U.S. health officials on Friday endorsed the first blood test that can help diagnose Alzheimer’s and identify patients who ...

The Trump administration has struck a deal to allow sales of a trigger mechanism that modifies a semiautomatic firearm to ...