Live Science12h
Scientists just made mice 'see-through' using food dye — and humans are next
A common food dye can turn the skin of living mice transparent, but we don't yet know if it'll work in humans.
The Financial1d
The Food and Drug Administration amended the emergency use authorization (EUA) of Novavax COVID-19 Vaccine
On August 30, 2024, the Food and Drug Administration amended the emergency use authorization (EUA) of Novavax COVID-19 Vaccine, Adjuvanted to include the updated 2024-2025 formula. The Novavax ...
News Medical2h
FDA set to regulate arsenic and cadmium in baby food
Rice and spinach are staples for babies' and young children's diets, but toxic metals and metalloids found in those foods can ...
Food Safety News2d
Congress should pass the Federal Food Administration Act
Listeria contamination is causing meats and produce to be pulled off store shelves nationwide, with hospitalizations and deaths continuing ...
STAT16d
Q&A: How the FDA could use AI for drug and device safety surveillance
Researchers suggest FDA could use artificial intelligence to enhance Sentinel, the agency's safety surveillance system for ...
The Business Journals11d
Food and Drug Administration Latest News
August 22, 2024, 2:35 PM ESTCommercial Real Estate December 14, 2022, 3:14 AM ESTHealth Care August 12, 2022, 2:46 PM ESTHealth Care June 24, 2022, 11:37 AM ESTHealth Care October 21, 2021, 12:22 ...
The Valdosta Daily Times11h
Amneal and Shilpa Announce U.S. FDA Approval of BORUZU™, the First Ready-to-Use Version of Bortezomib for subcutaneous administration
Amneal Pharmaceuticals, Inc. (Nasdaq: AMRX) (“Amneal” or the “Company”) and Shilpa Medicare Limited (“Shilpa”) announced U.S. Food and Drug Administration (FDA) approval of BORUZU ™, a new ...
Taiwan Food & Drug Administration Approves Moderna’s COVID-19 mRNA Vaccine Targeting the SARS-COV-2 Variant JN.1
Moderna, Inc. (NASDAQ:MRNA) today announced that the Taiwan Food & Drug Administration (FDA) has approved an updated formulation of the COVID-19 mRNA vaccine Spikevax, targeting the SARS-CoV-2 variant ...
Breakthrough Therapy designation for Sanbexin sublingual tablets granted by the United States Food and Drug Administration
Simcere Pharmaceuticals Group Ltd. (2096.HK) announced that Sanbexin Sublingual Tablets (Edaravone and Dexborneol sublingual tablets), an innovative drug for stroke, has been granted the Breakthrough ...
60% of baby and toddler food doesn’t meet nutrition standards, study finds
About 60% of packaged baby food sold in the United States doesn’t meet nutritional standards established by the World Health Organization, according to research published recently that opens a window ...
Alaska Dispatch News7h
Nearly 2,000 drug plants are overdue for FDA checks after COVID delays
The firms that are overdue for safety and quality inspections represent about 42% of the 4,700 plants that are currently ...
Yahoo Finance1mon
U.S. Food and Drug Administration Gives Huxley Medical 510(k) Clearance for SANSA Home Sleep Apnea Test
ATLANTA, Aug. 7, 2024 /PRNewswire/ -- Huxley Medical, a developer of technologies that streamline cardiopulmonary care, has received 510(k) clearance from the U.S. Food and Drug Administration ...