Federal agencies submit information collection requests to OMB for review and public comment to assess burden on businesses and the public.
FDA seeks 60 days of public comment on information collection requirements for Biologics License Applications under the Paperwork Reduction Act; deadline for comments is 60 days from Federal Register publication.
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Every rule is broken into specific to-dos with calendar dates.
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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 submitted a proposed information collection to OMB for Paperwork Reduction Act review regarding formal hearing administrative procedures and practices.
Coast Guard establishes a temporary safety zone on the Potomac River near Fairview Beach, Virginia for a fireworks display on July 11, 2026, prohibiting unauthorized vessels and persons from entering without Captain of the Port approval.
EPA finalizes hazardous air pollutant emission standards for plywood and composite wood products facilities, setting maximum achievable control technology limits for formaldehyde, acetaldehyde, and other HAP compounds at major source facilities.
Coast Guard establishes temporary safety zone in San Francisco Bay navigable waters on July 4, 2026, for fireworks display; vessel and personnel entry prohibited without Captain of the Port authorization.
EPA received pesticide product registration applications for new uses of currently registered active ingredients and solicits public comments on the April 2026 compilations.
EPA accepts public comments on new pesticide product registration applications containing previously unregistered active ingredients, with details on 2025 submissions under Federal Insecticide, Fungicide, and Rodenticide Act procedures.
Coast Guard enforces special local regulations for the Tiki Lee's Shootout on the River Airshow in Sparrows Point, MD from July 10 to 12, 2026, requiring vessel operators in the regulated area to comply with Patrol Commander directions.
FDA corrects contact information for the Expedited Investigational New Drug Pilot Program docket, which solicits public input on shortening timelines from drug identification to first-in-human clinical trials.
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