The Final Rule was mooted for implementation over a staged transition period, determined by a service’s risk level, by 2028.

FDA initiates removal of prescription fluoride tablets and drops amid concerns about gut microbiome effects, as Utah and ...

Trump's order seeks to ease regulations to compel more U.S. drug manufacturing. He also plans to assess tariffs on drug ...

On May 13, 2025, the U.S. Department of Health and Human Services (HHS) and the U.S. Food and Drug Administration (FDA) announced a public Request ...

Supposedly, the AI tool will speed up the FDA's drug review process by reducing the time its scientists have to spend doing ...

Op-ed views and opinions expressed are solely those of the author. Biotechadvancementsoftenfaceaysdue to bureaucracy, hindering the development of necessary therapies. Now is the time for us to […] ...

Galdieria extract blue, butterfly pea flower extract and calcium phosphate are three food colors from natural sources the FDA ...

The US Food and Drug Administration says it is starting the process to remove prescription fluoride tablets and drops from the market.

Burger chain In-N-Out has announced that it will remove artificial colorings and high-fructose corn syrup from its list of ...

The meetings appear to be part of a broader effort at the FDA to use this technology to speed up the drug approval process. “Why does it take over 10 years for a new drug to come to market?” ...

More than 75,000 cases of eye drops have been voluntarily recalled by a pharmaceutical testing lab after an audit by the Food & Drug Administration ... after the audit by the FDA, according ...

HHS, US FDA issue RFI on deregulatory plan to lower costs and empower providers: Silver Spring, Maryland Thursday, May 15, 2025, 09:00 Hrs [IST] The US Department of Health and Hu ...