🦠FDA Classifies Antimicrobial Susceptibility Testing Device as Class II
The Food and Drug Administration (FDA, the Agency, or we) is classifying the cellular analysis system for multiplexed antimicrobial susceptibility testing into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for the cellular analysis system for multiplexed antimicrobial susceptibility testing's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.
Learn More❌Cancellation of NIH Meeting on Biomedical Research Review
The notice announces the cancellation of a meeting for the National Institute of General Medical Sciences' Special Emphasis Panel, initially scheduled for July 2025, which focuses on the review of the Centers of Biomedical Research Excellence. The meeting has been transferred to the Center for Scientific Review.
Learn More📈SEC Notice on Miami Exchange Rule 1327 for Options Transfers
The SEC published a notice on the Miami International Securities Exchange's proposed Rule 1327, which aims to allow in-kind exchanges of options positions and ETF shares. This rule change addresses current limitations on transfers, potentially improving tax efficiency and operational capabilities for investment vehicles like ETFs and UITs, ultimately benefiting investors.
Learn More🐄Emergency Livestock Relief Program Regulations for 2023 and 2024
The final rule entitled Emergency Livestock Relief Program (ELRP) 2023 and 2024 was published on May 29, 2025. The Office of Management and Budget cleared the associated information collection requirements (ICR) on May 28, 2025. This document announces approval of the ICR.
Learn More📋Notice for Public Comments on GSA Qualitative Feedback Collection
Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division will be submitting to the Office of Management and Budget (OMB) a request to review and approve an extension of a previously approved information collection requirement regarding the Generic Clearance for the Collection of Qualitative Feedback on Agency Service Delivery.
Learn More📑Federal Acquisition Regulation Withdraws Small Business Participation Rules
OFPP, DoD, GSA, and NASA (collectively referred to as the Federal Acquisition Regulatory Council, or FAR Council) are withdrawing the proposed rule to amend the Federal Acquisition Regulation (FAR) titled: Small Business Participation on Certain Multiple-Award Contracts.
Learn More✈️Regulatory Changes for Standard Instrument Approach Procedures
This rule establishes, amends, suspends, or removes Standard Instrument Approach Procedures (SIAPS) and associated Takeoff Minimums and Obstacle Departure procedures (ODPs) for operations at certain airports. These regulatory actions are needed because of the adoption of new or revised criteria, or because of changes occurring in the National Airspace System, such as the commissioning of new navigational facilities, adding new obstacles, or changing air traffic requirements. These changes are designed to provide safe and efficient use of the navigable airspace and to promote safe flight operations under instrument flight rules at the affected airports.
Learn More📋Opportunity to Comment on CMS Information Collection Activities
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.
Learn More📉Consumer Product Safety Commission Seeks Input on Regulation Reduction
The Consumer Product Safety Commission (CPSC, or Commission) invites public comment on opportunities for the Commission to reduce burdens and costs of its existing rules, regulations, or practices without impacting safety.
Learn More💧Approval of Projects for Consumptive Water Use in Susquehanna Basin
This notice lists Approvals by Rule for projects by the Susquehanna River Basin Commission during the period set forth in DATES.
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