The seafood salad may be of particular risk to those customers who have an allergy or severe sensitivity to soy, the FDA has ...

In the US, liraglutide, semaglutide, and tirzepatide are currently under investigation for their ability to stimulate weight ...

The U.S. Food and Drug Administration (FDA) terminated a recall for Berkeley Club Beverages water on November 13 and recently ...

A soup mix recall issued this month has been updated by the U.S. Food and Drug Administration (FDA) as a Class I risk, the ...

The U.S. Food and Drug Administration (FDA) has announced a Class I recall—the agency's most serious level—for Atwater's Spider Web Tarts due to undeclared almonds, a tree nut allergen ...

As previously announced, the Company requested the Meeting in response to the FDA issuing a CRL, dated October 22, 2024, for the Company's Ketamine product's Abbreviated New Drug Application, which ...

TORONTO, Nov. 26, 2024 (GLOBE NEWSWIRE) -- PharmaTher Holdings Ltd. (the “Company” or “PharmaTher”) (OTCQB: PHRRF) (CSE: PHRM), a specialty pharmaceutical ...

The FDA has addressed our questions, paving the way for our Ketamine product’s new ... The forward-looking information contained in this press release is made as of the date hereof, and Company is not ...

The FDA updated the fludarabine phosphate injection labeling under Project Renewal, clarifying the dosage for combination ...

The FDA is scrutinising reports of haematological cancers in patients treated with bluebird bio's gene therapy for the rare ...