Public access to government records that document the handling of illnesses, faulty products, and safety lapses at health facilities will slow after mass firings at the federal Department of Health ...

A few days earlier, Peter Marks, the medical doctor who led the division of the Food and Drug Administration ... of public service,” says Jennifer Jones, director of the Center for Science ...

The initiative, which will start with monoclonal antibodies, is the first big regulatory shift from the FDA since Martin ...

“The cuts in all of our agency are not affecting science,” Kennedy told ABC ... for Disease Control and Prevention and the Food and Drug Administration. On Wednesday, HHS did not respond ...

Further, we do not assign journalists to cover topics in respect of which they have disclosed a financial interest ... approval of such drugs by the US Food and Drug Administration (FDA) and ...

The US Food and Drug Administration announced Thursday that it will be phasing out a requirement that monoclonal antibodies ...

The U.S. Food and Drug Administration is replacing animal testing with human-relevant methods, including artificial ...

The U.S. Food and Drug Administration said on Thursday it plans to replace animal testing in the development of monoclonal ...

A former top FDA official said it’s only a matter of time before the chaos at the agency starts to impact drug reviews.

Cytochrome P450 (CYP) proteins are responsible for breaking down more than 80% of all Food and Drug Administration ...

The move comes after lawmakers sought to force the agency to update regulations that would allow alternatives to animal ...

On Thursday, shares in Charles River Laboratories, a leading contract research organizations that has stirred controversy ...