Meanwhile, in an executive order, Trump created his long-discussed “Department of Government Efficiency,” to be led by Elon ...
Palvelussamme on juuri nyt häiriö, yritäthän myöhemmin uudelleen. Pahoittelemme aiheutunutta haittaa.
Abeona Therapeutics Inc.'s promising gene therapy for RDEB, potential FDA approval, undervalued stock, and key risks. Click ...
The FDA has given marketing authorization to Zyn nicotine pouches. That doesn't necessarily mean they're safe to use, ...
The U.S. Food and Drug Administration (FDA) has been playing catch-up on three long-delayed proposed rules required under the Modernization ...
This comes after two dozen food and safety advocates filed a 2022 petition ... though the FDA does list the substance as an ...
The US Food and Drug Administration (FDA)’s recently issued final rule establishing application, labeling, and postmarketing reporting ...
FDA shared updates on the healthy claim, a proposed FOP nutrition label, and more to help meet the goals of the White House ...
Sources predict required front-of-pack labeling could mean giving up key real estate in costly redesigns — or, more ...
Food and Drug Administration officials granted a 2022 petition ... requires FDA to ban any additive found to cause cancer in people or animals. The dye is known as erythrosine, FD&C Red No. 3 or Red 3 ...
Berkley, Lakeville, New Bedford and Rochester have interim compliance, meaning they’ve either submitted their action plans or have already established the zones and filed their compliance ...
The FDA banned the controversial red dye no. 3, which gives food and drinks a bright, cherry red color. The ban is a response to a 2022 petition ... drugs have a compliance date of Jan. 18 ...