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.
FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.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.
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. 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.
OMB review process for federal regulations requires public comment submissions; the comment period deadline and specific regulatory details are not specified in the title alone.
Farm Service Agency seeks public comments on a revised information collection for General Program Administration to verify applicant eligibility, authorized loan use, and government security interests under the Paperwork Reduction Act.
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.
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.
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