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🌍Notice of Approved Resource Management Plan for Rio Puerco Field Office

The Bureau of Land Management (BLM) announces the availability of the Record of Decision (ROD) for the Approved Resource Management Plan (RMP) for the Rio Puerco Field Office located in central and northwestern New Mexico. The BLM Director signed the ROD on December 23, 2024, which constitutes the decision of the BLM and makes the Approved RMP effective immediately.

⚖️EPA Notice

The Environmental Protection Agency (EPA) has submitted an information collection request, Toxic Substances Control Act (TSCA) Section 8(b) Reporting Requirements for TSCA Inventory Notifications (EPA ICR Number 2565.05 and OMB Control Number 2070-0201), to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act (PRA). This is a proposed extension of the ICR, which is currently approved through January 31, 2025. Public comments were previously requested via the Federal Register on Tuesday, April 23, 2024. This notice allows for an additional 30 days for public comments.

✈️FAA Extends Compliance Date for U.S. Agent Designation Rules

On October 8, 2024, the FAA published a final rule that will require individuals with foreign addresses and no U.S. physical address on file with the FAA who apply for certain certificates, ratings, or authorizations to designate a U.S. agent for service. This final rule extends the deadline for those individuals to designate a U.S. agent for service from January 6, 2025, to April 2, 2025. This final rule does not apply to individuals with foreign addresses who currently hold certain certificates, ratings, or authorizations, as the compliance date for those individuals continues to be July 7, 2025.

💊FDA Meeting

The Food and Drug Administration's (FDA, Agency, or we) Office of Pediatric Therapeutics, the Center for Drug Evaluation and Research, and the Center for Biologics Evaluation and Research are announcing a public meeting entitled "Interested Parties Meeting: Implementation of the Best Pharmaceuticals for Children Act and Pediatric Research Equity Act." The purpose of the public meeting is to seek input from interested parties, including patient/parent/ caregiver groups, consumer groups, regulated industry, academia, and others. This input will enable FDA to obtain any recommendations or information relevant to the report to Congress that FDA is required to submit concerning pediatric drug and biologic development and labeling, as outlined in section 508 of the Food and Drug Administration Safety and Innovation Act (FDASIA).

📄Federal Acquisition Regulation on Rerepresentation of Small Business Status

DoD, GSA, and NASA are issuing a final rule amending the Federal Acquisition Regulation (FAR) to implement regulatory changes made by the Small Business Administration to order-level size and socioeconomic status rerepresentation requirements.

⚛️NRC Issues License Renewal for Monticello Nuclear Plant

The U.S. Nuclear Regulatory Commission (NRC) has issued Subsequent Renewed Facility Operating License No. DPR-22 to Northern States Power Company, a Minnesota corporation (NSPM, or the licensee), for Monticello Nuclear Generating Plant, Unit 1 (Monticello). In addition, the NRC has prepared a record of decision (ROD) that supports the NRC's decision to issue Subsequent Renewed Facility Operating License No. DPR-22.

🦠Reopening Comment Period for Avian Influenza EIS - USDA Notice

We are reopening the comment period for our notice advising the public that a draft programmatic environmental impact statement (EIS) has been prepared by the Animal and Plant Health Inspection Service relative to our response activities to highly pathogenic avian influenza (HPAI) outbreaks in commercial and backyard poultry operations located throughout the United States, including the U.S. territories. The draft EIS analyzes and compares the potential environmental effects of using three action alternatives during an HPAI outbreak. This action will allow interested persons additional time to prepare and submit comments.

🏥CMS Lab Personnel Report

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.

📊Amended Antidumping Duty Notice for Superabsorbent Polymers

On December 17, 2024, the U.S. Court of International Trade (CIT) issued its final judgment in Ad Hoc Coalition of American SAP Producers v. United States, Court No. 23-00010, sustaining the U.S. Department of Commerce's (Commerce) final remand redetermination pertaining to the less-than-fair-value (LTFV) investigation of certain superabsorbent polymers (SAP) from the Republic of Korea (Korea) covering the period of investigation October 1, 2020, through September 30, 2021. Commerce is notifying the public that the CIT's final judgment is not in harmony with Commerce's final determination in that investigation, and that Commerce is amending the final determination and the resulting antidumping duty (AD) order with respect to the dumping margins assigned to LG Chem, Ltd. (LGC) and all other producers and exporters of subject merchandise.

💰NYSE Chicago Connectivity Fee Schedule Proposed Rule Change