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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 ...
The mass cuts, which included communications staff, could slow public notices on medical device recalls and other safety ...
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Medical Device Network on MSNFDA grants breakthrough device status for Elucent’s EnVisio X1 systemThe 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 ...
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 ...
Distributors, dispensers, and retailers of medical device products face a patchwork of federal and state requirements ...
Vinay Prasad will be the next director of the FDA's Center for Biologics Evaluation and Research, after Peter Marks was forced out.
Neuralink has received the U.S. Food and Drug Administration's "breakthrough" tag for its device to restore communication for ...
U.S. health officials on Friday endorsed the first blood test that can help diagnose Alzheimer’s and identify patients who ...
Patients who put their lives in the hands of healthcare institutions and personnel do so with an unmitigated amount of trust, ...
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