FDA’s requirement for truthful, balanced risk and benefit information applies to drugmakers, leaving a loophole for both ...

The U.S. Food and Drug Administration spent more than 15 years crafting the ... A new bill in Congress would compel the FDA ...

The day after the election, some celebrated Trump's win and RFK Jr.'s potential role as a public health decision-maker. Why?

The FDA designated 166 products under its breakthrough devices program in its most recent financial year, reversing the ...

Nov 13 (Reuters) - The U.S. Food and Drug Administration approved PTC Therapeutics ... The drugmaker will also get the FDA's ...

Facing with a dialogue with RFK Jr., a top FDA official mounts a public defense of vaccines — and pleads for open minds.

The FDA Modernization Act of 1997 established the Fast Track designation to expedite developing and reviewing new drugs ...

Investors and entrepreneurs will track decisions affecting drugs, medical devices and telehealth.

A key reason positions haven't been filled is that they require travel that ranges from 25% to 75% of the time.

Recently, two notable incidents—a listeria outbreak involving ready-to-eat meat products and an E. coli outbreak tied to ...

The U.S. Food and Drug Administration's ("FDA") new advisory committee on digital health is set to examine its approach for evaluating and ...

As federal health scientists await an unprecedented takeover by medical skeptics in the second Trump administration, some are ...