On May 2, 2025, and notwithstanding the FDA’s invitation to submit the sBLA articulated by its leadership at the January Meeting, the FDA delivered an RTF letter.

The case centered on venue-shopping and whether the tobacco company R.J. Reynolds could appeal in the 5th Circuit appeals ...

Colorado bakers ponder FDA plan to phase out petroleum-based synthetic food dyes 03:02. The U.S. Food and Drug Administration announced plans to phase out all petroleum-based synthetic food dyes ...

FDA approves powerful HIV drug with the potential to end the epidemic in the U.S. My Husband Died Abroad. As I Boarded The Plane Home, A Flight Attendant's Innocent Comment Broke Me. Los Angeles Mayor ...

ROCK ISLAND ARSENAL, Ill. — U.S. Army Secretary Daniel Driscoll visited the Rock Island Arsenal on Monday. His visit follows ...

When St. Petersburg native and local business owner Christina Kiss finished her own post-hurricanes cleanup, she reflected on ...

FDA’s long-standing accelerated approval program generally issues decisions in six months for drugs that treat life-threatening diseases. Regular drug reviews take about 10 months.

Robert F. Kennedy Jr. warned Food and Drug Administration staff about the influence of the “deep state” on the agency in an all-hands meeting Friday where he also made off-color comments about ...

For the new program, the FDA will issue a limited number of “national priority vouchers” to companies “aligned with U.S. national priorities,” the agency said in a statement.

Robert F. Kennedy Jr. warned Food and Drug Administration staff about the influence of the “deep state” on the agency in an all-hands meeting Friday where he also made off-color comments about ...

For the new program, the FDA will issue a limited number of “national priority vouchers” to companies “aligned with U.S. national priorities,” the agency said in a statement.