Coast Guard enforces a safety zone during the Super Boat Grand Prix in Michigan City, Indiana from August 1–2, 2026, prohibiting unauthorized entry, transit, or anchoring in the regulated area.
Federal agencies submit information collection requests to OMB for review and public comment to assess burden on businesses and the public.
Tell Bizmoon what your business does and we'll cut the Federal Register down to what actually matters.
Every rule is broken into specific to-dos with calendar dates.
We tell you which parts of your business each rule actually touches.
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.
The FCC prohibits importation and marketing of communications equipment designated as covered products in 2024 or earlier due to national security risks.
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.
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.
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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