Notice 19 Aug 2025 regulatory compliance, natural gas, federal energy regulatory commission, pipeline, southern california gas company

💡Combined Notice of Natural Gas Pipeline Rate Filing Implications

The Department of Energy's Federal Energy Regulatory Commission issued a notice regarding new natural gas pipeline rate filings. It outlines the submissions by Southern California Gas Company, including rate revisions for offshore delivery services. The document provides details for public engagement and protest filing deadlines, emphasizing the importance of compliance with regulatory procedures.

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Notice 19 Aug 2025 market data, trading, exchange, regulatory compliance, cboe

📈Cboe Introduces New All Cancels Report for Traders

The Cboe BZX Exchange proposes a new All Cancels Report as part of the Cboe Timestamping Service, designed to provide an in-depth analysis of cancel behavior for market participants. This report will assist firms in improving their trading strategies by offering detailed insights into their cancel message activities.

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Proposed Rule 19 Aug 2025 regulatory compliance, fda, food additives, animal feed, microorganisms, evonik corporation

🐾Evonik Corporation Files Food Additive Petition for Animal Use

The Food and Drug Administration (FDA or we) is announcing that we have filed a food additive petition, submitted by Evonik Corporation, proposing that we amend our food additive regulations to provide for the safe use of Bacillus velezensis as a source of viable microorganism in animal food for all species.

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Notice 19 Aug 2025 agriculture, regulatory compliance, usda, fees, financial implications, grain inspection

🌾Impact of 2025/2026 Grain Inspection and Weighing Service Fees

The Agricultural Marketing Service (AMS or the Agency) is announcing the 2025/2026 rates it will charge for official grain inspection and weighing services, supervision of official grain inspection and weighing services, and miscellaneous fees for other services performed under the United States Grain Standards Act (USGSA), as amended. This action publishes the resulting fees from the annual review of fees. The 2025/2026 hourly, unit, and tonnage rates will be applied at the beginning of the fiscal year. This action establishes the rates for user-funded services based on costs incurred by AMS. This year, cost-based analyses indicated the need to increase certain user fee rates when current rates are insufficient to cover the costs of providing the service. While cost-saving measures have and will continue to be implemented, user fee rate increases are necessary to offset rising operational costs and rebuild the user fee reserve. Prospective customers can find the fee schedule posted on the Agency's public website: https://www.ams.usda.gov/about-ams/fgis-program- directives.

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Notice 19 Aug 2025 regulatory compliance, nuclear energy, texas, energy sector, construction permits

⚛️NRC Establishes Board for Long Mott Energy Reactor Permit Review

The Nuclear Regulatory Commission has established an Atomic Safety and Licensing Board to oversee the permit proceedings for Long Mott Energy, LLC's proposed four-unit reactor facility in Texas. This formal notice addresses a hearing request from a local environmental group and specifies the composition of the Board overseeing the case.

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Notice 19 Aug 2025 regulatory compliance, aviation, faa, air safety, engineering data, stc

✈️FAA Notice on Abandonment of John Benham STC and Data Access

This notice announces the FAA's intent to designate John Benham Supplemental Type Certificate (STC) No. SA3866SW as abandoned and make the related engineering data available upon request. The FAA has received a request to provide engineering data concerning this STC. The FAA has been unsuccessful in contacting John Benham concerning the STC. This action is intended to enhance aviation safety.

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Notice 19 Aug 2025 regulatory compliance, fda, debarment, drug importation, illegal drugs

🚫FDA Debars Doyal Kalita for 10 Years from Drug Importation

The Food and Drug Administration (FDA) is issuing an order under the Federal Food, Drug, and Cosmetic Act (FD&C Act) debarring Doyal Kalita for a period of 10 years from importing or offering for import any drug into the United States. FDA bases this order on a finding that Mr. Kalita was convicted of two felony counts under Federal law. The factual basis supporting Mr. Kalita's conviction, as described below, is conduct relating to the importation into the United States of a drug or controlled substance. Mr. Kalita was given notice of the proposed debarment and was given an opportunity to request a hearing to show why he should not be debarred. As of June 26, 2025 (30 days after receipt of the notice), Mr. Kalita had not responded. Mr. Kalita's failure to respond and request a hearing constitutes a waiver of his right to a hearing concerning this matter.

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Notice 19 Aug 2025 regulatory compliance, ohio, environmental management, advisory board, public participation, clean-up activities

🏛️Department of Energy

This notice announces an in-person meeting of the Environmental Management Site-Specific Advisory Board (EM SSAB), Portsmouth. The Federal Advisory Committee Act requires that public notice of this meeting be announced in the Federal Register.

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Notice 19 Aug 2025 regulatory compliance, fda, cdc, public workshop, drug manufacturing, feedback, industry best practices

💊FDA Workshop on CMC Development

The Food and Drug Administration (FDA, the Agency, or we) is announcing a virtual-only public workshop entitled "Lessons Learned From the Chemistry, Manufacturing, and Controls (CMC) Development and Readiness Pilot (CDRP) Program." This workshop fulfills a commitment in the seventh authorization of the Prescription Drug User Fee Act (PDUFA VII) to hold a public meeting to discuss best practices and lessons learned from this pilot program. Convened by the Duke-Robert J. Margolis, MD Center for Health Policy (Duke-Margolis) and supported by a cooperative agreement between FDA and Duke-Margolis, the workshop will feature sponsors and FDA experience under this pilot program and will solicit input on future directions for FDA policy and programs to facilitate expedited CMC development of products under an investigational new drug application (IND), where indicated based upon the anticipated clinical benefits.

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Proposed Rule 19 Aug 2025 regulatory compliance, faa, safety, aircraft, aviation safety, incorporation by reference, air transportation, airworthiness directive, maintenance

✈️FAA Proposes New Airworthiness Directive for ATR Airplanes

The FAA proposes to adopt a new airworthiness directive (AD) for all ATR--GIE Avions de Transport R[eacute]gional Model ATR42 and Model ATR72 airplanes. This proposed AD was prompted by a design review that determined that the inspection interval of the pressure regulator and shut-off valve (PRSOV) functional test must be reduced to meet the design safety objectives, due to a risk of dormant failures. This proposed AD would require repetitive functional tests of each PRSOV, and applicable corrective actions. The FAA is proposing this AD to address the unsafe condition on these products.

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