Federal health officials have widened a recall of a dietary supplement linked to a salmonella outbreak, warning that the product was also sold to consumers in U.S. territories and the United Kingdom ...
The FDA clears triage tool by Aidoc that detects 14 acute conditions from CT scans to improve emergency care workflows.
The Advanced Research Projects Agency for Health (ARPA-H) is soliciting proposals to develop two agentic AI assistants for ...
Opna Bio has received the US FDA orphan drug designation for OPN-2853, a BET small molecule inhibitor, to treat myelofibrosis.
The recalled tuna was sold under the brand name Genova and includes two varieties: Genova Yellowfin Tuna in Olive Oil and ...
FDA approves first brain stimulation device for home depression treatment. Flow Neuroscience's FL-100 headset uses electrical ...
On Wednesday, radiology AI company Aidoc announced the FDA has cleared a tool that can triage 14 critical findings in a ...
The FDA issued draft guidance Jan. 21 proposing the use of minimal residual disease and complete response as primary endpoints to support accelerated approval of drugs for multiple myeloma. The draft ...
The SonoMotion platform will be showcased at booth 1508 during the 2026 American Urological Association meeting.
The FDA approved external trigeminal nerve stimulation (TNS) in 2019 as the first non-drug device for treating ADHD, ...
For years, the federal government advised Americans to limit red meat and foods high in saturated fats. However, new federal ...
A plan to slash Food and Drug Administration drug review times is raising alarms at the public health agency that's been ...
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