🚛FMCSA Proposes CDL Standards Exemption for Military Technicians
FMCSA proposes to amend the Federal Motor Carrier Safety regulations (FMCSRs) to allow dual-status military technicians to qualify for the exception for certain military personnel from commercial driver license (CDL) standards. This rulemaking responds to a petition for rulemaking submitted by James D. Welch.
Learn More🛣️FHWA Proposes to Rescind Federal-Aid Contract Requirements
FHWA is proposing to rescind the rule and regulations issued on September 30, 1974, Federal-Aid Contracts (Appalachian Contracts).
Learn More📡FCC Petition for Reconsideration
Petitions for Reconsideration (Petition) have been filed in the Commission's proceeding by Kara R. Curtis on behalf of Aerospace and Flight Test Radio Coordinating Council, Inc. and by Ari Q. Fitzgerald et al. on behalf of GE HealthCare Technologies Inc.
Learn More🚌FMCSA Proposes Removal of Obsolete Water Carrier References
FMCSA proposes to remove all obsolete references to "water carriers" in the FMCSA regulations (FMCSRs). FMCSA does not specifically regulate water carriers except to the extent that such carriers also engage in motor carrier operations. In such cases, the existing FMCSRs provide appropriate coverage of the carrier's motor carrier operations.
Learn More🎖️Proposed Information Collection for Vietnam War Commemoration Program
In compliance with the Paperwork Reduction Act of 1995, the WHS announces a proposed public information collection and seeks public comment on the provisions thereof. Comments are invited on: whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; the accuracy of the agency's estimate of the burden of the proposed information collection; ways to enhance the quality, utility, and clarity of the information to be collected; and ways to minimize the burden of the information collection on respondents, including through the use of automated collection techniques or other forms of information technology.
Learn More🛢️Public Scoping Session for Mountain Valley Pipeline Amendment Project
The Federal Energy Regulatory Commission (FERC) announces a public scoping session to gather comments on environmental issues related to the Mountain Valley Pipeline Amendment Project. This scoping process aims to address potential environmental impacts and encourages community input regarding the construction and operation of the pipeline facilities in Virginia and North Carolina.
Learn More📄Preliminary Determination on Paper File Folders from Cambodia
The U.S. Department of Commerce (Commerce) preliminarily determines that paper file folders from Cambodia are not being, or are not likely to be, sold in the United States at less than fair value (LTFV). The period of investigation (POI) is October 1, 2023, through September 30, 2024. Interested parties are invited to comment on this preliminary determination.
Learn More🌿FDA Notice on Poppy Seeds Regulation and Comment Period Extension
The Food and Drug Administration (FDA) is correcting a notice that appeared in the Federal Register on April 9, 2025. The document announced the extension of the comment period for the request for information entitled "Growing, Harvesting, Processing, and Distribution of Poppy Seeds--Industry Practices Related to Opiate Alkaloids." The notice published with an error in the ADDRESSES section. This document corrects the error.
Learn More📈SEC Extends Review Period for Cboe BZX ETF Rule Change
The SEC issued a notice regarding a proposed rule change from Cboe BZX Exchange, which seeks to allow in-kind creations and redemptions for various cryptocurrency ETFs, including the Franklin Bitcoin and Ethereum ETFs. The SEC has extended the review period to July 10, 2025, to fully evaluate the implications raised by the proposal.
Learn More📄FDA's Draft Guidance for Electronic Submission of Medical Device Q-Submissions
The Food and Drug Administration (FDA or Agency) is announcing the availability of the draft guidance entitled "Electronic Submission Template for Medical Device Q-Submissions." FDA is issuing this draft guidance to introduce submitters of certain Q-Submissions (Q-Subs), specifically Pre-Submissions (Pre-subs) to the Center for Devices and Radiological Health (CDRH) and Center for Biologics Evaluation and Research (CBER), to the current resources and associated content developed and made publicly available to support Pre-Sub electronic submissions to FDA. This draft guidance, when finalized, is intended to represent one of several steps in meeting FDA's commitment to the development of electronic submission templates to serve as guided submission preparation tools for industry to improve submission consistency and enhance efficiency in the review process. This draft guidance is not final nor is it for implementation at this time.
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