🍷Treasury Notice on Alcohol and Tobacco Tax Information Collection
The Department of the Treasury will submit the following information collection requests to the Office of Management and Budget (OMB) for review and clearance in accordance with the Paperwork Reduction Act of 1995, on or after the date of publication of this notice. The public is invited to submit comments on these requests.
Learn More🚬FDA Notice on Reporting Harmful Constituents in Tobacco Products
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Learn More⚖️Analysis of Designation of Antifa as Domestic Terrorist Organization
The regulatory text outlines an order designating Antifa as a domestic terrorist organization due to its calls for violent overthrow of governmental systems and organized campaigns against law enforcement. It emphasizes coordination with other entities to suppress lawful political activity and encourages enforcement actions against associated illegal operations. The order also clarifies its implementation is subject to applicable law without creating enforceable rights against the United States.
Learn More🦌Information Collection Notice on Zoonotic Disease Risk in Agriculture
The Department of Agriculture seeks public comments on an information collection regarding human-deer interactions related to SARS-CoV-2. This effort, authorized under federal wildlife services regulations, aims to assess risks and behaviors that may lead to disease spillover, impacting wildlife management and public health strategies.
Learn More⚗️FDA Notice
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Learn More🌫️EPA Approves Washington Regional Haze SIP
The Environmental Protection Agency (EPA) is approving the regional haze State implementation plan (SIP) revision, submitted by Washington on January 28, 2022, to address applicable requirements under the Clean Air Act (CAA) and the EPA's Regional Haze Rule (RHR) for the regional haze program's second implementation period.
Learn More🧬FDA Guidance on Postapproval Safety and Efficacy for CGT Products
The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft document entitled "Postapproval Methods to Capture Safety and Efficacy Data for Cell and Gene Therapy Products; Draft Guidance for Industry." The draft guidance document discusses methods and approaches for capturing postapproval safety and efficacy data for cell and gene therapy (CGT) products. Given the potential for long-lasting effects of CGT products, and the generally limited number of participants treated in clinical trials, the collection of postapproval study data for CGT products is important for gathering data on product safety and effectiveness over time.
Learn More🌊Rescission of Expired Grace Period for BOEM Data Extensions
On August 12, 2025, the Bureau of Ocean Energy Management (BOEM) published a final rule that removed reference to an expired grace period for data extensions. Some of the language from this section was inadvertently erased. This document corrects the final regulations.
Learn More📦FDA Requires Tracking for Food Import Notifications
The Food and Drug Administration (FDA, the Agency, or we) is issuing a final rule to amend its prior notice regulation to add a requirement that prior notice and food facility registration information be submitted within a certain timeframe after certain notices of refusal or hold have been issued ("post-refusal" and "post-hold" submission) or responses to requests for FDA review have been issued and beginning October 1, 2026, add a requirement that the prior notice for articles of food arriving by international mail include the name of the mail service and a mail tracking number. The rule will also finalize certain technical changes, including those that reflect expanded capabilities of the Automated Broker Interface/Automated Commercial Environment/International Trade Data System (ABI/ACE/ITDS) and the Prior Notice Systems Interface (PNSI). These amendments will improve program efficiency and better enable FDA to protect the U.S. food supply and public health.
Learn More🏥CMS Proposes Information Collection Activities; Comments Requested
The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS' intention to collect information from the public. Under the Paperwork Reduction Act of 1995 (PRA), federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information (including each proposed extension or reinstatement of an existing collection of information) and to allow 60 days for public comment on the proposed action. Interested persons are invited to send comments regarding our burden estimates or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.
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