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.
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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 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.
Farm Service Agency requests public comments on revised information collection requirements for Emergency Conservation Program and Biomass Crop Assistance Program eligibility, cost-share agreements, and payment certification.
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.
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.
HUD seeks OMB approval for a public housing waiting list data collection tool under the Housing Opportunity Through Modernization Act; public comment period ends 30 days from publication.
HUD seeks public input on the availability of domestically manufactured products for federally funded housing and infrastructure projects under the Build America, Buy America Act.
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