The FDA regulates more than three-quarters of the U.S.’ food supply. All color additives must be approved by the FDA before they are used in food sold in the U.S. There are 36 FDA-approved color ...

filed requests in 2022 to have the Food and Drug Administration remove approval for the polio vaccine ... was nominated to be the Trump administration's head of the Department of Health and Human ...

Opposition councillors have expressed their discomfort at plans to loan a prominent Northampton shopping centre £3m, as cabinet members have backed the financial proposals. West Northamptonshire ...

The Iredell-Statesville Schools Board of Education approved the change to turf and a new track at the high school at a cost of more than $3.3 million. The motion passed by a 6-1 vote, with board ...

the FDA has provided guidance on a potential path to meet the regulatory standard for substantial evidence of effectiveness supporting accelerated approval. The FDA recommended that Clene ...

“We are very pleased to reach agreement with the FDA on core components of an Accelerated Approval pathway for AMT-130,” said Walid Abi-Saab, M.D., chief medical officer of uniQure.

Listen to Story Congress's Manickam Tagore, Saptagiri Sankar Ulaka wear PM, Adani face masks Rahul Gandhi questions their actions, mocks relationship Opposition again stage protests in Parliament ...

While the FDA has claimed that red 3, like other additives the agency has approved, can be safe to consume, advocates have long called for its ban amid concerns that the food dye is linked to ...

AbbVie has completed a hat trick of phase 3 wins for its Parkinson’s disease prospect tavapadon, teeing the drugmaker up to file for FDA approval in 2025. The Big Pharma acquired the once-daily ...

REUTERS The lawsuit said, “the medical and scientific community and the public have a substantial interest in reviewing the data and information underlying the FDA’s approval of the Pfizer ...

The new findings showed improvements in HbA1c, hypoglycemia, body weight, and systolic blood pressure with sotagliflozin in this patient population, though the risk of diabetic ketoacidosis continues ...

The FDA is reviewing data from the phase 3 ALLELE study (ClinicalTrials.gov Identifier: NCT03394365), which assessed the efficacy and safety of tabelecleucel for the treatment of EBV+ PTLD in the ...