- As recently covered on this blog, FDA issued a final determination stating that
CONGRESS
Untitled
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Congress questions FDA policy regarding the publication of Untitled Letters.
- FDA has the authority to issue two types of letters to regulated entities: Warning Letters and Untitled Letters. FDA issues
Friday Follow-Up
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House Agricultural Committee votes to repeal COOL requirements.
- As covered on this blog earlier this week, the World Trade Organization (WTO) rejected the U.S. appeal of a ruling regarding the
Antibiotic Ask
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- For years, FDA and the animal feed industry have grappled with how to address
Beauty and the Bill
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Bipartisan bill introduced to expand FDA’s authority over cosmetic products.
- Although FDA currently has authority to regulate cosmetic products marketed in the United States, regulatory action in this space has
Mr. Schneiderman Goes to Washington
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State AGs ask Congress to crack down on dietary supplements.
- Earlier this year, New York’s Attorney General (AG) launched a probe into the dietary supplement industry, targeting major retailers for
Federal GM Bill Reintroduced
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Bill to prohibit states from requiring GM labeling reintroduced in Congress. (subscription to Law 360 required)
- In recent years, we have seen a variety of federal, state, and local
Anti-Antibiotics
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Bill introduced in Senate to combat overuse of antibiotics in food-producing animals.
- For years, FDA and various stakeholders have grappled with how best to reduce the use of medically important