Canadian National Railway Company petitioned the Federal Railroad Administration for an extension of regulatory relief from periodic testing requirements on vital microprocessor-based signal systems.
CSX Transportation petitioned the Federal Railroad Administration for an extension waiving periodic testing requirements on microprocessor-based signal systems.
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Every rule is broken into specific to-dos with calendar dates.
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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.
FAA airworthiness directive requires Boeing 737-8, 737-9, and 737-8200 operators to revise flight manuals to prohibit radio altimeter-dependent operations in Canadian airspace due to 5G Lower C-Band interference risks.
FAA airworthiness directive mandates Boeing 747 series airplane flight manual revisions to prohibit operations requiring radio altimeter data in Canadian airspace due to 5G Lower C-Band interference risks during critical flight phases.
SEPTA petitioned the Federal Railroad Administration for an extension of regulatory relief regarding daily post-trip tests and periodic maintenance inspections.
Investment company seeks deregistration under Section 8(f) of the Investment Company Act after completing liquidating distributions to shareholders on November 29, 2025, with $140,000 in liquidation expenses.
FMCSA is accepting public comments on the National School Transportation Association's application to renew an exemption allowing school bus CDL applicants to skip the under-the-hood vehicle inspection requirement; restricted to intrastate school bu…
CFTC and SEC request public comment on expanding portfolio and cross-margining frameworks for securities and derivatives under their joint jurisdiction.
NMFS Southwest Fisheries Science Center applied for a research permit to conduct marine mammal studies at its La Jolla, California facility under File No. 29287.
FDA classifies monitors for opioid-induced impairment of oxygenation as class II medical devices, subject to special controls to ensure safety and effectiveness.
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