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.
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After healthcare come the capital-heavy sectors: trade, transportation, energy, and finance. If you operate in one of them, the volume of change is relentless.
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.
FAA supersedes prior airworthiness directives for Airbus Helicopters Models AS332C, AS332C1, AS332L, and AS332L1 by requiring modification of cabin lateral sliding plug door release or jettison systems to terminate repetitive inspections.
FAA airworthiness directive mandates repetitive inspections and corrective actions for fastener holes in Airbus A321-251NX through A321-272NX center fuselage frame foot joints due to manufacturing process deviations.
FAA airworthiness directive requires Airbus Helicopters AS350 series operators to inspect cargo hook gaps and replace affected units or prohibits their installation to address safety non-conformities.
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…
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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