FDASIA was signed into law on July 9, 2012. This piece of legislation grants FDA the authority to collect user fees from industry to fund reviews of drugs, devices, and biologics. The changes to ...
Silver Spring, MD, July 10, 2026 (GLOBE NEWSWIRE) -- The U.S. Food and Drug Administration today issued a proposed rule that, if finalized, would create a streamlined registration pathway for ...
In the wake of the Food & Drug Administration’s (FDA) ambitious unified agenda, on July 13, 2026, the agency published a proposed rule aiming to align its regulatory frameworks with “how distributed ...
In the ever-changing regulatory landscape that alcohol manufacturers must navigate, the regulations imposed by the U.S. Food and Drug Administration (FDA) are often overlooked. But breweries, ...
U.S. and foreign human and animal food facilities that are required to register with the U.S. Food and Drug Administration must renew their registration this year before Dec. 31. The FDA said in a ...
A new cross-center draft guidance document released by the US Food and Drug Administration (FDA) established the agency's preferred unique facility identification (UFI) system used to register ...
Cosmetics Update: FDA Publishes Draft Guidance on Cosmetic Product Facility Registration and Listing
Our FDA and Food & Beverage teams outline key requirements of the Modernization of Cosmetics Regulation Act (MoCRA) and provide key takeaways from the Food and Drug Administration’s new draft guidance ...
The US Food and Drug Administration (FDA) has issued a final rule regarding electronic device registration and listing requirements, putting into practice a long-awaited rule combining the ...
The U.S. Food and Drug Administration (FDA) finalized a rule as part of the implementation of the Food Safety Modernization Act (FSMA) to improve the accuracy of the food facility registration ...
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