For instance, to the general public, reputational damage from FDA’s mishandling of food safety is frequently blurred into distrust toward the broader agency, including the divisions that oversee drug safety. With Robert F. Kennedy Jr. potentially ...
The U.S. Food and Drug Administration has approved Symvess, the first acellular tissue engineered vessel indicated fo
A discussion of the development of consumer protection law in the US through the enactment of key legislation and formation of the Food and Drug Administration (FDA).
Most of the recalls are contamination or allergen-based. While 2025 is near, there are still callbacks to be aware of. Here is a list of December recalls according to the FDA. FDA
Bird Flu Update
· 1d · on MSN
FDA begins testing raw cheese for bird flu
Bird Flu Update As FDA Begins Cheese Screening
The FDA has begun testing cheese for bird flu as human cases of the virus continue to rise in the United States.
FDA to begin testing raw milk cheese for contamination with bird flu
The Food and Drug Administration has begun a domestic sampling assignment to collect and test aged raw milk cheese for Highly Pathogenic Avian Influenza
The U.S. Food and Drug Administration said on Friday that it has approved an injectable version of Bristol Myers Squibb's blockbuster cancer drug, Opdivo. Opdivo is part of a class of drugs called PD-1 inhibitors,
Consumers who take copies of the weight loss drug Zepbound and diabetes drug Mounjaro will need to find a new source for these medications.
A proposed rule would require makers of talc-containing cosmetic products to test for asbestos via an analytical approach
The Food and Drug Administration approved Eli Lilly’s weight-loss drug Zepbound on Dec. 27 to treat sleep apnea, a common but potentially serious sleep-related breathing disorder, making it the first medication for certain patients with the condition.
Kolaleh Eskandanian, chief innovation officer at Children’s National Hospital, said the partnership is meant to address the many challenges with developing devices for children and infants.
The Food and Drug Administration (FDA) is being sued in two lawsuits after releasing its Final Rule on Laboratory Developed Tests (LDTs). The
FDA representatives have urged Congress to review its request for funding as it embarks on a more modern reassessment of chemicals.
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