In December, the U.S. Food and Drug Administration (“FDA”) announced that it had issued a letter to the dietary supplement ...

On January 21, the US Food and Drug Administration (FDA) issued a draft guidance clarifying the agency’s authority to access ...

The Food and Drug Administration commissioner's effort to drastically shorten the review of drugs favored by President Donald ...

Generally Recognized as Safe reform, food chemical safety reviews, and expanding the role of state agencies in the food ...

Experts say two new guidances — issued without the usual public comment period — leave questions about how patients will navigate a growing pool of wearables.

In 2022, the Modernization of Cosmetics Regulations Act of 2022 (MoCRA) was signed into law, bringing about the largest expansion of the U.S. Food ...

The US Food and Drug Administration has issued a Request for Information (RFI) on labeling and preventing cross-contact of gluten in packaged food. The FDA is seeking information on adverse reactions ...

WASHINGTON — The American Civil Liberties Union (ACLU) filed a lawsuit yesterday to compel the Food and Drug Administration (FDA) to disclose records related to the agency’s review of its regulations ...

The "Navigating EU (European Union) and FDA (Food and Drug Administration) Regulations for Drug/Device and Device/Drug Combination Products Training Course (Mar 2nd - Mar 3rd, 2026)" training has been ...

The Senate Health, Education, Labor, and Pensions Committee, chaired by Sen. Bill Cassidy, R-Louisiana, held a hearing about ...

CTK recently completed FDA OTC registration and related compliance steps for three white-label suncare products: a sun lotion, sun stick, and sun serum. “OTC” refers to drug products that can be ...