Federal regulations
- Temporary Placement of 7-Hydroxymitragynine Above a Specified Threshold in Schedule I; Request for InformationJuly 6, 2026
The Office of the Assistant Secretary for Health seeks public comments on a proposed threshold for scheduling 7-hydroxymitragynine under the Controlled Substances Act.
- Agency Information Collection Activities; Submission to the Office of Management and Budget (OMB) for Review and Approval; Comment Request; Request for Duty-Free Entry of Scientific Instrument or ApparatusJuly 6, 2026
The U.S. Customs and Border Protection requests public comment on a revised information collection form for duty-free entry of scientific instruments and apparatus; comments due 30 days from Federal Register publication.
- Expedited Investigational New Drug Pilot Program; Request for Information; CorrectionJuly 6, 2026
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.
- Determination That VASOPRESSIN IN SODIUM CHLORIDE (vasopressin) 0.9%, Injection, 50 units/50 milliliters (1 unit/milliliters) Was Not Withdrawn From Sale for Reasons of Safety or EffectivenessJuly 6, 2026
FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.
- Endo Operations Limited, et al.; Withdrawal of Approval of 34 New Drug ApplicationsJuly 6, 2026
FDA withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.
- Atlantic Highly Migratory Species; Atlantic Bluefin Tuna Fisheries; Closure of the Angling Category Southern New England Area Trophy Fishery for 2026July 6, 2026
NMFS closes the Atlantic bluefin tuna angling category trophy fishery in Southern New England for 2026 for fish measuring 73 inches or greater curved fork length.
- Carbon and Certain Alloy Steel Wire Rod from Mexico: Final Results of Antidumping Duty Administrative Review; 2023-2024July 6, 2026
U.S. Department of Commerce finds that Mexican carbon and alloy steel wire rod producers made sales below normal value during the October 1, 2023 through September 30, 2024 review period.
- Certain Corrosion-Resistant Steel Products From the People's Republic of China: Initiation of Circumvention Inquiry on the Antidumping and Countervailing Duty OrdersJuly 6, 2026
The U.S. Department of Commerce is investigating whether corrosion-resistant steel products from China completed in Thailand circumvent existing antidumping and countervailing duty orders.
- Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Premarket Approval of Medical DevicesJuly 6, 2026
The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.
- Submission for OMB Review; Comment RequestJuly 6, 2026
I need the description to create an accurate summary. Please provide the description field for this OMB submission document.
Track Federal regulations for your business
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.
No legal jargon. Read the impact in two sentences.
Email + dashboard pings the moment something changes.
Healthcare draws more federal rulemaking than any other sector
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.
Federal rulemaking
- Healthcare and life sciences
- Trade and commerce
- Transportation and aviation
- Energy and utilities
- Finance
- Natural resources
- Other