News

FDA Greenlights Game-Changing UV Technology That Could Make Raw Milk Safer to Consume
Tamarack Biotics’ TruActive process targets pathogens with UV light while keeping the milk’s enzymes and proteins intact.
Prescott eNews2hOpinion
Interchangeable Medicine, or Inaccessible Medicine? – Inside Sources
Medicines derived from living cells — biologics — are some of the most expensive medicines in America. What keeps prices ...
The Daily Northwestern3hOpinion
Anne: FDA’s approval of Juul is a step backward in the fight to protect youth
The U.S. Food and Drug Administration made the controversial decision to authorize the sale of Juul e-cigarettes, including ...
FDA Suspends Muscular Dystrophy Drug After 3 Patient Deaths
The U.S. Food and Drug Administration ( FDA) has placed an immediate clinical hold on Sarepta Therapeutics' investigational ...
Colorado Public Radio23h
Synthetic Psilocybin nears FDA review, signaling a potential shift in American mental healthcare
Supporters believe that FDA approval will make the drug more accessible. Right now, traditional psilocybin therapy offered at healing centers in the state is not covered by insurance.
Las Vegas Sun1d
Juul’s FDA approval doesn’t clear fog of e-cigarette risks, especially for teens
The Food and Drug Administration has granted permission for Juul to continue selling its e-cigarettes, offering some reprieve ...
Sarepta tells FDA it won’t halt shipments despite patient deaths
In a highly unusual move, Cambridge-based Sarepta said late Friday won’t comply with a request from the Food and Drug ...
Gene therapy maker Sarepta tells FDA it won’t halt shipments despite patient deaths
Drugmaker Sarepta Therapeutics says it won’t comply with a request from U.S. regulators to halt all shipments of its gene ...
Sarepta Therapeutics crisis is huge blow to Duchenne families, company
Sarepta rebuffed a call from the Food and Drug Administration to halt all shipments of its gene therapy for Duchenne muscular ...
Sarepta says it won't comply with FDA request to stop shipping gene therapy Elevidys
U.S. regulators asked Sarepta Therapeutics on Friday to voluntarily halt shipments of its Elevidys gene therapy after a ...
The FDA's Newest Approval Could Have A Major Impact On Your Favorite Foods
Move over, artificial food colors, the FDA just approved gardenia (genipin) blue, a plant‑derived dye to shake up drinks and ...
Rutgers University2d
FDA Clears First Blood Test for Alzheimer’s Diagnosis, a “Turning Point” in Early Detection
Unlike expensive positron emission tomography (PET) scans or invasive lumbar punctures, the new blood test measures the ratio ...