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.
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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.
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DEA issues temporary scheduling order placing 7-hydroxymitragynine above a specified threshold in Schedule I, subjecting manufacturers, distributors, importers, exporters, and researchers to Schedule I controlled substance regulations and penalties.
The Drug Enforcement Administration announces temporary scheduling of mitragynine pseudoindoxyl, MGM-15, and MGM-16 as Schedule I controlled substances, restricting manufacturing, distribution, possession, and research activities.
The ATF is withdrawing its direct final rule on licensee "eZ Check" verification for transfers that was published May 6, 2026, in response to adverse comments.
ATF proposes amending NFA registration requirements to exempt manufacturers from registering firearms made for U.S. Government contracts and allow late registration if those firearms fall out of contract.
ATF proposes allowing firearms applicants to submit photo ID copies instead of passport-style photographs and streamlining fingerprint card requirements to one card for most applicants.
Federal Communications Commission invites public comment on information collection requirements under the Paperwork Reduction Act, with specific focus on reducing burdens for small businesses with fewer than 25 employees.
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