FAA seeks public comment on renewing OMB approval for flight attendants' Fatigue Risk Management Plans required from Part 121 certificate holders under the FAA Reauthorization Act of 2018.
FDA seeks 60 days of public comment on information collection requirements for extralabel drug use in animals under the Paperwork Reduction Act.
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After healthcare come the capital-heavy sectors: trade, transportation, energy, and finance. If you operate in one of them, the volume of change is relentless.
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 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.
The Council on Environmental Quality publishes a notice of availability for environmental impact statements on proposed federal projects and actions affecting small businesses and communities.
FAA announces charter renewal and membership nominations for the National Airspace System Advisory Committee, which advises on air traffic management systems and integration of new aviation technologies.
EPA exempts resin acids, esters with glycerol (CAS No. 8050-31-5) from tolerance requirements when used as a surfactant inert ingredient in pesticide formulations on growing crops and raw agricultural commodities.
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