MARAD solicits public comment on a request to operate the foreign-built small passenger vessel S/V KINGSLEY in U.S. coastwise trade carrying no more than twelve passengers for hire.
MARAD solicits public comments on a request to permit the foreign-built vessel S/V LADY SUSAN to operate in U.S. coastwise trade carrying no more than 12 passengers for hire, to determine potential adverse effects on domestic vessel builders and coa…
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The Maritime Administration invites public comments on a determination request for the foreign-built M/V MEAT WAGON 2 to operate in U.S. coastwise trade carrying up to twelve passengers for hire.
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.
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FDA determines that vasopressin 0.9% injection was not withdrawn for safety or effectiveness reasons, allowing approval of generic abbreviated new drug applications if other regulatory requirements are met.
The Office of the Assistant Secretary for Health seeks public comments on a proposed threshold for scheduling 7-hydroxymitragynine under the Controlled Substances Act.
Multiple federal agency forms are undergoing Paperwork Reduction Act review to assess and potentially reduce reporting burdens on small businesses and other respondents.
FDA submitted a proposed information collection to OMB for Paperwork Reduction Act review regarding formal hearing administrative procedures and practices.
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