Search Results for keywords:"Regulations"

The Food and Drug Administration (FDA) is inviting the public to comment on a proposed collection of information related to its Generic Drug User Fee Program. This proposal is part of fulfilling requirements under the Paperwork Reduction Act, which mandates a 60-day public comment period for proposed information collections. Comments can be submitted online through https://www.regulations.gov or via mail by March 17, 2025. The FDA seeks feedback on the necessity, accuracy, and methods of the information collection, and aims to support the implementation of its program through the information gathered.

In a notice from the Federal Reserve System, several companies applied to become bank holding companies or to acquire banks or bank holding companies. These applications are in accordance with the Bank Holding Company Act of 1956 and the regulations included. The public can inspect the applications and related files at designated Federal Reserve Banks and the Board of Governors' offices. Comments on the applications are invited from the public and must be submitted by January 13, 2025, with all responses being subject to public disclosure.

The Food and Drug Administration (FDA) has announced that certain Food Contact Notifications (FCNs) are no longer effective because some manufacturers stopped using the listed substances for food contact in the U.S. The FDA is following a set process that allows them to determine when an FCN is no longer in use. They expect all remaining stocks of these substances, which were last produced or supplied before January 6, 2025, to be used up by June 30, 2025, as a measure to protect public health. The FDA updated its inventory of effective and no longer effective FCNs on their website.

Merck, Sharp & Dohme LLC submitted a proposal to the Foreign-Trade Zones Board to conduct production activities at its facility in Rahway, New Jersey. The request was reviewed according to the Board's regulations, and the public was invited to comment. On January 16, 2024, the Board decided no further review was needed, and the production activity was authorized under existing regulations. The notification was officially documented on January 16, 2025.

The Pipeline and Hazardous Materials Safety Administration (PHMSA) of the Department of Transportation has announced the decisions on applications for special permits related to hazardous materials. This notice informs the public about whether these permits have been granted or denied. Comments on these actions need to be submitted by March 26, 2025. For more details, people can contact Donald Burger at the PHMSA or visit the Records Center in Washington, DC.

The Federal Crop Insurance Corporation published a correcting amendment to a rule that changes certain insurance provisions for crops like sunflower seed and dry pea. Originally, the amendments were published on November 30, 2020, but some changes were not properly included in the official regulations. This document fixes those errors by correcting dates, removing a repetitive word, and updating phrases within the insurance provisions. The changes to the regulation are effective starting February 24, 2021.

The Pipeline and Hazardous Materials Safety Administration (PHMSA) is announcing a list of applications for new special permits related to hazardous materials transportation. These permits are being processed according to the Department of Transportation's Hazardous Material Regulations. The public has until April 25, 2025, to submit comments on these applications. For more information, individuals can contact Donald Burger at the PHMSA.

The Centers for Medicare & Medicaid Services (CMS) has approved the American Association for Accreditation of Ambulatory Surgery Facilities, known as QUAD A, to continue as a national accrediting organization for Outpatient Physical Therapy (OPT) programs involved in Medicare or Medicaid. QUAD A revised its standards and processes to ensure compliance with Medicare requirements, such as conducting thorough surveys and ensuring facilities meet necessary regulations. This approval is effective from April 4, 2025, to April 4, 2030. The notice confirms that QUAD A’s standards meet or exceed Medicare’s conditions, allowing accredited facilities to be deemed compliant.

The Commerce Department's Bureau of Industry and Security (BIS) implemented new export control rules to manage the global distribution of advanced artificial intelligence (AI) models and computing technologies. These rules introduce tighter controls on exporting certain AI model weights and advanced computing chips to protect national security. The measures include new licensing requirements, exceptions, and procedures for companies to follow when exporting these technologies. Additionally, BIS aims to balance securing these technologies with allowing their beneficial uses, ensuring that they are shared responsibly and securely.

The Securities and Exchange Commission (SEC) has announced that on February 27, 2025, NYSE Arca, Inc. filed a proposed rule change to amend its Connectivity Fee Schedule. The change reflects the renaming of NYSE Chicago, Inc. to NYSE Texas, Inc. This proposal has been designated for immediate effectiveness, meaning it does not significantly affect investor protection or competition and will take effect immediately to align with a related rule change by NYSE Chicago. The SEC is inviting public comments on this proposal to ensure it is consistent with existing regulations.