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.
The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.
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FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.
FDA withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.
The U.S. Department of Commerce issues a countervailing duty order on steel concrete reinforcing bar from Algeria following an affirmative final determination.
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.
U.S. Department of Commerce amends its antidumping duty order on common alloy aluminum sheet from Türkiye following a June 17, 2026 Court of International Trade decision affecting the dumping margin assigned to Assan Aluminyum.
New York's Administrative Declaration of Disaster dated June 30, 2026, covers severe storms and flooding and may trigger state and federal disaster assistance programs for affected small businesses.
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.
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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