U.S. Department of Commerce maintains countervailing duty orders on common alloy aluminum sheet from Bahrain, India, and Türkiye after determining that revocation would likely result in continuation or recurrence of countervailable subsidies.
U.S. Commerce Department maintains antidumping duty orders on seamless carbon and alloy steel pipe from Czech Republic, South Korea, Russia, and Ukraine after finding revocation would likely result in continued or recurring dumping.
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 U.S. Department of Commerce maintains an antidumping duty order on standard steel welded wire mesh from Mexico, finding that revocation would likely result in continuation or recurrence of dumping.
U.S. Department of Commerce determines that antidumping duty orders on common alloy aluminum sheet from 16 countries will continue to prevent dumping recurrence based on expedited sunset review findings.
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.
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.
The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.
FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.
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.
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.
No legal jargon. Read the impact in two sentences.
Email + dashboard pings the moment something changes.