Sarepta Therapeutics (SRPT) stock drops as the company faces potential FDA-mandated studies after safety concerns over its ...

But it’s unclear if the evidence provided to support continued use of fluoridated supplements will matter. The FDA said in ...

By Kingsley Webora TANKEH Bureaucratic bottlenecks and high regulatory costs at the Food and Drugs Authority (FDA) are discouraging many small- and medium-sized enterprises (SMEs) from obtaining the ...

How Mahoning County Public Health district tests mosquitoes for West Nile Virus in Austintown, Ohio New Photos Show How ...

Tabelecleucel, an allogeneic, EBV-specific T-cell immunotherapy, works by targeting and eliminating EBV-infected cells.

Nootropics are substances that enhance cognitive performance through various mechanisms, including cholinergic, glutamatergic, and dopaminergic pathways. They include prescription medications, natural ...

Andrew Bailey's lawsuit, filed in Cole County Circuit Court, claims that Planned Parenthood is downplaying the safety issues of mifepristone. Planned Parenthood responded that Bailey has repeatedly ...

New York City, NY, July 24, 2025 (GLOBE NEWSWIRE) -- Feedback from a recent survey shows that men and women who use ...

As lawmakers in Texas weigh whether to criminalize intoxicating hemp products containing any detectable amount of THC, a Texas Democrat has introduced a new bill that would legalize and regulate ...

The FDA's 'Elsa' AI, intended to speed up drug approvals, is reportedly fabricating studies, part of a wider trend of unreliable AI in high-stakes roles.

Bypassing its standard pathways for scientific discussions, FDA has recently held a slew of so-called "expert panels" that ...

Insiders at the Food and Drug Administration are ringing alarm bells over the agency's use of an AI to fast-track drug ...