Notice 21 Aug 2025 sec, risk management, financial regulations, clearing agency, u.s. treasury securities

💵ICC Application for Clearing Agency Registration Under SEC

The Securities and Exchange Commission is reviewing an application from ICE Clear Credit LLC to register as a clearing agency for U.S. Treasury securities. This application outlines ICC’s proposed operational structure, risk management strategies, and the establishment of a Treasury Guaranty Fund, inviting public comment on the regulatory implications for market participants.

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Rule 21 Aug 2025 regulatory compliance, healthcare, fda, laboratories, medical devices, biologics, cancer risk assessment

🧬FDA Classifies Cancer Predisposition Risk Assessment Systems

The Food and Drug Administration (FDA, the Agency, or we) is classifying the cancer predisposition risk assessment system 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 classification of the cancer predisposition risk assessment system. We are taking this action because we have determined that classifying the device into class II 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.

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Notice 21 Aug 2025 regulatory compliance, pharmaceutical industry, importation, controlled substances, drug enforcement

💊Catalent CTS, LLC DEA Importer Application Overview

Catalent CTS, LLC. has applied to be registered as an importer of basic class(es) of controlled substance(s). Refer to Supplementary Information listed below for further drug information.

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Notice 21 Aug 2025 sec, exchange, regulation, investment, nasdaq, etf, cryptocurrency

📈SEC Notice on CoinShares XRP ETF Listing Review Extension

The SEC issued a notice regarding the proposed rule change by Nasdaq to list and trade shares of the CoinShares XRP ETF. This follows the agency's decision to extend the review period for that proposal, allowing more time for consideration of related issues before a final decision is made.

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Proposed Rule 21 Aug 2025 environmental regulation, environmental protection, reporting and recordkeeping requirements, incorporation by reference, business compliance, intergovernmental relations, air pollution control, air quality, sulfur oxides, iowa, sulfur dioxide

🌬️EPA Proposes Redesignation of Muscatine, IA Air Quality Status

The Environmental Protection Agency (EPA) is proposing to redesignate the nonattainment area in Muscatine County, Iowa to attainment for the 2010 1-hour sulfur dioxide (SO<INF>2</INF>) National Ambient Air Quality Standard (NAAQS). The EPA is also proposing to approve Iowa's maintenance plan for the 2010 1-hour SO<INF>2</INF> NAAQS for the Muscatine nonattainment area and approve modifications to source-specific permits in the Iowa State Implementation Plan (SIP). The EPA's proposed approval of this rule revision is being done in accordance with the requirements of the Clean Air Act (CAA).

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Rule 21 Aug 2025 healthcare, regulation, fda, medical devices, class ii devices, menopause test

🧪FDA Classifies Menopause Test System Under Class II Regulations

The Food and Drug Administration (FDA, Agency, or we) is classifying the menopause test system 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 classification of the menopause test system. We are taking this action because we have determined that classifying the device into class II 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.

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Rule 21 Aug 2025 regulation, fda, laboratories, medical devices, health industry, biologics, bacterial vaginosis, vaginitis

🩺FDA Classifies Device for Detecting Vaginitis-Related Microorganisms

The Food and Drug Administration (FDA, the Agency, or we) is classifying the device that detects nucleic acid sequences from microorganisms associated with vaginitis and bacterial vaginosis 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 device that detects nucleic acid sequences from microorganisms associated with vaginitis and bacterial vaginosis's classification. We are taking this action because we have determined that classifying the device into class II 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.

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Proposed Rule 21 Aug 2025 compliance, regulations, aviation, faa, safety, aircraft, aviation safety, incorporation by reference, air transportation, airworthiness directives, gulfstream

✈️Proposed Airworthiness Directive for Gulfstream Aircraft – FAA NPRM

The FAA proposes to adopt a new airworthiness directive (AD) for all Gulfstream Aerospace LP Model Gulfstream 100, Astra SPX, and 1125 Westwind Astra airplanes. This proposed AD was prompted by a determination that new airworthiness limitations are necessary. This proposed AD would require revising the existing maintenance or inspection program, as applicable, to incorporate new airworthiness limitations. The FAA is proposing this AD to address the unsafe condition on these products.

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Rule 21 Aug 2025 regulation, fda, food safety, medical devices, food industry, cosmetics, color additives, drugs, foods, beverage industry

🍹FDA Confirms Galdieria Extract Blue as Safe Color Additive

The Food and Drug Administration (FDA or we) is confirming the effective date of June 26, 2025, for the final order that appeared in the Federal Register of May 12, 2025. The final order amends the color additive regulations to provide for the safe use of galdieria extract blue as a color additive at levels consistent with good manufacturing practice (GMP) in: non-alcoholic beverages and beverage bases, fruit drinks, fruit smoothies, fruit juices, vegetable juices, dairy-based smoothies, milk shakes and flavored milks, yogurt drinks, milk-based meal replacement and nutritional beverages, breakfast cereal coatings, hard candy, soft candy and chewing gum, flavored frostings, ice cream and frozen dairy desserts, frozen fruits, water ices and popsicles, gelatin desserts, puddings and custards, whipped cream, yogurt, frozen or liquid creamers (including non-dairy alternatives), and whipped toppings (including non-dairy alternatives).

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Proposed Rule 21 Aug 2025 environmental regulation, environmental protection, epa, reporting and recordkeeping requirements, incorporation by reference, business compliance, intergovernmental relations, ozone, air pollution control, volatile organic compounds, air quality, nitrogen dioxide, particulate matter, permits, lead, sulfur oxides, carbon monoxide, alabama

🌬️EPA Proposes Revision to Alabama Air Permit Regulations

The Environmental Protection Agency (EPA) is proposing to approve a revision to the Alabama State Implementation Plan (SIP) submitted by the Alabama Department of Environmental Management (ADEM) on December 20, 2023. The proposed SIP revision consists of minor changes to certain air permit regulations that have been revised by the State agency since EPA last approved those provisions. EPA is proposing to approve the SIP revision pursuant to the Clean Air Act (CAA or Act).

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