FDA issues Emergency Use Authorizations for two animal drugs to prevent and treat New World screwworm infestations in livestock, poultry, and exotic animals following HHS's August 18, 2025 public health emergency declaration.
NMFS implements North Carolina's 2026 commercial summer flounder quota transfer to Virginia under the Summer Flounder, Scup, and Black Sea Bass Fishery Management Plan.
NMFS establishes final 2026 harvest specifications for salmon in Cook Inlet's exclusive economic zone to conserve resources under the Magnuson-Stevens Fishery Conservation and Management Act.
FDA seeks 60 days of public comment on information collection requirements for extralabel drug use in animals under the Paperwork Reduction Act.
FDA submission to OMB for Paperwork Reduction Act review of information collection requirements for dietary supplement manufacturing, packaging, labeling, and holding operations.
FDA requests OMB clearance for information collection activities related to Current Good Manufacturing Practice regulations for Type A medicated articles and medicated feeds under the Paperwork Reduction Act of 1995.
The FDA renews its Science Board advisory committee for an additional two years, with the new charter expiring June 26, 2028.
FDA withdraws approval of SpecGx LLC's abbreviated new drug application for Methylphenidate Hydrochloride Extended-Release tablets in 27mg, 36mg, and 54mg strengths per the applicant's request.
FDA classifies radiological machine learning-based quantitative imaging software with predetermined change control plans as Class II medical devices, subject to special controls to ensure safety and effectiveness.
NMFS implements shallow-water grouper catch limits and recreational closed seasons for Gulf of America fisheries to reduce scamp and yellowmouth grouper harvest pending Amendment 58A development.
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