The U.S. House of Representatives Committee on Energy and Commerce Subcommittee on Health will hold a legislative hearing on April 29, 2026, ...

The FDA meeting announcement​ follows repeated pledges by Health Secretary Robert F. Kennedy Jr. to loosen regulations on ...

The FDA has quietly proposed legislation that would give it more authority to deem drugs misbranded in pharma DTC ads. But ...

Just before the change in administration, the Food and Drug Administration (FDA) made headlines by revoking approvals to use the color additive FD&C Red Dye No. 3 in food after January 15, 2027. This ...

President Donald Trump's administration is reclassifying state-licensed marijuana as a "less-dangerous" drug, Acting Attorney ...

This seems like an appropriate time to talk about what can be done to improve FDA regulation so that mobile app development can flourish. First I’ll tackle current events that make this a good time to ...

Over the last couple years, FDA has clarified the scope of its regulation over mobile health. In the agency’s September 2013 guidance, FDA spelled out its oversight for some of the most common mobile ...

Areas like generic drug regulation, drug supply chain and clinical trials reporting may be in need of some revamping by the Food and Drug Administration, according to a new Work Plan from the U.S.

Artificial intelligence has the potential to fundamentally change healthcare, and the possibilities are neither radical nor ...

When a patient in an early-phase drug trial experiences a serious side effect today, weeks or even months can pass before ...

The US Food and Drug Administration (FDA) is authorized to regulate foods, dietary supplements, drugs, devices (including in vitro diagnostic), biologics, veterinary products, cosmetics and tobacco ...

The FDA has gained a reputation during the past year for being inconsistently flexible, particularly when it comes to rare diseases. Executives at Rezolute and CERo Therapeutics recently had positive ...