In a statement on Tuesday, 11 February, the SFA reported detecting sennosides in Susenji MOFA+ and sibutramine in Fabulous ...
Gilead Sciences, Inc. today announced that the U.S. Food and Drug Administration (FDA) has accepted its New Drug Application (NDA) submissions for lenacapavir?the company's twice-yearly injectable HIV ...
Berlin Heals Holding AG, a late stage MedTech start up, has developed a breakthrough method and a product for the therapy of ...
Industry executives sounded somewhat optimistic at the Mido eyewear trade show as the category proves resilient against a ...
VANCOUVER - The B.C. Labour Relations Board has found Starbucks wrongfully made "threats of adverse consequences" against an ...
The OnePlus Watch 3 adds hardware support for ECG, but it wasn't approved for users in the United States or Canada.
The U.S. Food and Drug Administration has made an update to its MadeGood granola bar recall. The popular granola bars, sold on Amazon and in stores like Target, Whole Foods, Wegmans, CVS ...
The U.S. Food and Drug Administration approved Merilog as biosimilar to Novolog for the improvement of glycemic control in adults and pediatric patients with diabetes mellitus. “Merilog ...
The U.S. Food and Drug Administration issued the highest risk classification to its Pearl Milling Company pancake and waffle mix recall. The Quaker Oats Company initially issued a recall on Jan ...
WASHINGTON — The Trump administration’s effort to slash the size of the federal workforce reached the Food and Drug Administration this weekend, as recently hired employees who review the ...
With no fanfare after 89 reported sick, the FDA has closed its investigation into a romaine lettuce E. coli outbreak without telling the public more and the CDC continues to remain mum.
Roche (RHHBY) announced that the Food and Drug Administration has approved a New Drug Application for an Evrysdi tablet for people living with spinal muscular atrophy. “Evrysdi is the only non ...