FDA's Cellular, Tissue, and Gene Therapies Advisory Committee will hold a public meeting to review Capricor's biologics license application for Deramiocel, a cell therapy product, with public comment accepted via docket submission.
Department of Commerce seeks 60 days of public comment on vessel monitoring systems type-approval information collection requirements before OMB submission under the Paperwork Reduction Act.
NMFS proposes removing a 9-mile Santa Clara River reach from critical habitat protection for Southern California steelhead under the Endangered Species Act following a petition from United Water Conservation District.
Southeast Data, Assessment, and Review Steering Committee meets to discuss stock assessment processes and schedules for South Atlantic, Gulf of America, and Caribbean fisheries.
SEDAR 100 public meeting process for Gulf gray triggerfish assessment includes data workshop, webinars, and review workshop to inform Southeast fisheries management decisions.
NMFS proposes to restrict directed commercial Pacific sardine fishing off Washington, Oregon, and California for July 1, 2026 through June 30, 2027, allowing harvest only as live bait, minor directed fisheries, incidental catch, or under exempted pe…
U.S. Commerce Department continues antidumping and countervailing duty orders on commodity matchbooks from India to prevent dumping and material injury to domestic matchbook manufacturers.
FDA determines the regulatory review period for VYALEV human drug product patent extension purposes and publishes this notice as required by law.
Caribbean Fishery Management Council's Scientific and Statistical Committee holds a two-day virtual meeting to address fishery management agenda items.
FDA classifies medial knee implanted shock absorbers as Class II devices subject to special controls to ensure safety and effectiveness while reducing regulatory burden for manufacturers.
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