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The U.S. Department of Commerce has preliminarily determined that Samyoung Fitting Co., Ltd. from Korea sold forged steel fittings in the U.S. at prices lower than their normal value during the period from December 1, 2022, to November 30, 2023. The department invites feedback on these findings, and the final results will guide future antidumping duties and deposits. Interested parties can submit comments, and a hearing may be requested. The preliminary results were published on March 21, 2025, and the final decision is expected within 120 days of this publication.

The Federal Reserve System announces that several individuals have applied to acquire shares of a bank or bank holding company under the Change in Bank Control Act. The applications are available for public inspection at the Federal Reserve Bank of Richmond and the Board of Governors. People interested in commenting on the applications can send their views to the respective locations by January 3, 2025. Comments will be publicly disclosed and should exclude any confidential information.

The Federal Reserve System received applications from several individuals and trusts to acquire shares of Guaranty Bancorp, Inc., and Woodsville Guaranty Savings Bank, both located in Woodsville, New Hampshire. The public can inspect the application details and other filings at the indicated Federal Reserve Banks or on the Board of Governors' website. Comments about the applications must be submitted by March 13, 2025, and will be publicly disclosed without alterations, so personal or confidential information should not be included.

The Food and Drug Administration (FDA) has released draft guidance on how in vitro diagnostic devices (IVDs) should be validated during emergencies involving emerging pathogens, declared under Section 564. This guidance is currently in draft form and not yet ready for implementation. It gives general recommendations for testing devices to ensure they are accurate and reliable during health crises like disease outbreaks. The FDA encourages public comments on the draft by March 10, 2025, either electronically or by mail, before finalizing the guidance.

Aveva Drug Delivery Systems, Inc. has applied to the Drug Enforcement Administration, a part of the Justice Department, to register as an importer of certain controlled substances. They intend to import these substances solely for analytical purposes and not for commercial sale. Interested parties can submit their comments or objections electronically, or request a hearing, by February 27, 2025. The registration is subject to specific regulations and permits as outlined in federal laws.

The Federal Maritime Commission has announced the filing of an agreement under the Shipping Act of 1984. This agreement, known as the Maersk/Network Shipping Ltd. Ad Hoc Space Charter Agreement, allows Maersk A/S and Network Shipping, Ltd. to share cargo space between ports in Costa Rica, Ecuador, Guatemala, and California. The agreement was filed by Wayne Rohde from Cozen O'Connor and is proposed to take effect on February 3, 2025. Anyone interested can review the agreement online and submit comments to the Commission within 12 days, or 7 days for expedited review requests.

The National Marine Fisheries Service (NMFS), part of the National Oceanic and Atmospheric Administration (NOAA), has announced a public meeting of the Permanent Advisory Committee (PAC) on March 18, 2021. The PAC advises U.S. Commissioners to the Commission for the Conservation and Management of Highly Migratory Fish Stocks in the Western and Central Pacific Ocean (WCPFC). The meeting will discuss the results of the 2020 WCPFC session and U.S. priorities for the 2021 session, focusing on tropical tuna management and other relevant issues. The meeting will be held via web conference, and the public is invited to attend or submit comments by March 13, 2021.

The Centers for Medicare & Medicaid Services (CMS) is inviting public comments on their plan to collect information, as required by the Paperwork Reduction Act of 1995. The public has 60 days to comment on the proposed information collection activities, including estimates of the burden and suggestions to improve the quality and clarity of the data collection. CMS is seeking feedback on two main collections: the application for participation in the Intravenous Immune Globulin (IVIG) Demonstration and the collection of encounter data from MA organizations. Comments can be submitted electronically or by regular mail.