FDA submission to OMB for Paperwork Reduction Act review of information collection requirements for dietary supplement manufacturing, packaging, labeling, and holding operations.
FDA requests OMB clearance for information collection activities related to Current Good Manufacturing Practice regulations for Type A medicated articles and medicated feeds under the Paperwork Reduction Act of 1995.
The FDA renews its Science Board advisory committee for an additional two years, with the new charter expiring June 26, 2028.
FDA withdraws approval of SpecGx LLC's abbreviated new drug application for Methylphenidate Hydrochloride Extended-Release tablets in 27mg, 36mg, and 54mg strengths per the applicant's request.
FDA issues Emergency Use Authorizations for two animal drugs to prevent and treat New World screwworm infestations in livestock, poultry, and exotic animals following HHS's August 18, 2025 public health emergency declaration.
NHTSA denied petition DP21-003 requesting investigation of alleged runaway throttle and speed control defects in Kia and Hyundai vehicles, finding insufficient evidence that accelerator systems violate Federal Motor Vehicle Safety Standards.
MARAD is soliciting comments on a request to operate the foreign-built vessel S/V Purple Pelican in U.S. coastwise trade carrying up to twelve passengers for hire to assess potential adverse effects on U.S. vessel builders and domestic maritime oper…
FAA announces charter renewal and membership nominations for the National Airspace System Advisory Committee, which advises on air traffic management systems and integration of new aviation technologies.
PHMSA seeks comments on revised incident, accident, and annual report forms for gas and hazardous liquid pipeline facilities plus the National Pipeline Mapping System under the Paperwork Reduction Act.
FDA seeks 60 days of public comment on information collection requirements for extralabel drug use in animals under the Paperwork Reduction Act.
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