MARAD is soliciting public comments on a request to operate the foreign-built small passenger vessel S/V GRACIE in U.S. coastwise trade to determine potential adverse effects on domestic vessel builders and coastwise operators.
MARAD is soliciting public comments on a request to operate the foreign-built vessel M/V DEUCE in U.S. coastwise trade carrying no more than twelve passengers for hire, to assess potential impacts on U.S. vessel builders and coastwise trade operator…
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.
FDA submitted a proposed information collection to OMB for Paperwork Reduction Act review regarding formal hearing administrative procedures and practices.
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 withdraws approval of 34 new drug applications across multiple applicants whose manufacturers requested withdrawal due to discontinued marketing.
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.
North Carolina amends the using and controlling agency designations for restricted airspace areas R-5301, R-5302A, R-5302B, and R-5302C without changing boundaries, altitudes, or operational parameters.
NHTSA grants Rivian's petition that MY 2022 electric delivery van noncompliance with Federal Motor Vehicle Safety Standard No. 208 is inconsequential to motor vehicle safety.
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