A discussion of the development of consumer protection law in the US through the enactment of key legislation and formation ...

The Food and Drug Administration (FDA) will begin collecting samples of raw cow’s milk cheese from across the U.S. to test ...

A Class I recall is used when "a violative product will cause serious adverse health consequences or death," according to the ...

A nationwide recall of enchiladas has been announced after the U.S. Food and Drug Administration (FDA) identified a potential ...

The proposed rule is required under a law passed by Congress last year, and is intended to ensure the safety of makeup and ...

Zepbound, a drug approved by the FDA, has been shown to reduce the severity of obstructive sleep apnea in obese adults, ...

The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's ...

Dichloromethane, a volatile solvent commonly used in industrial applications, has been banned in products in many areas, ...

After plugging billions into its manufacturing network to meet rampant demand for Mounjaro and Zepbound, Eli Lilly is looking ...

Security is strengthened by reducing the attack surface, but this also makes the submission process far more user-friendly.

FDA approves the first subcutaneous version of nivolumab, making PD-1 inhibitors available to new groups of patients.

More than three years after Novartis’ plan for a speedy approval for intrathecal Zolgensma was thwarted by an FDA requirement ...