Regulatory Changes, Financial Assistance 8 Jan 2025 compliance, regulation, small business, investment, financial services
Regulatory Compliance, Financial Implications 8 Jan 2025 compliance, sec, financial regulation, self-regulatory organizations, audit trail fees, investors exchange
Notice 7 Jan 2025 compliance, information collection, atf, department of justice, firearms training

📄DOJ Notice on Firearm Training Request Information Collection

The Department of Justice (DOJ), The Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF), will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995.

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Compliance, Regulatory Requirements 7 Jan 2025 compliance, regulation, federal trade commission, financial institutions, identity theft prevention

🛡️FTC Proposes Extension of Red Flags, Card Issuers, and Address Rules

The Federal Trade Commission ("FTC" or "Commission") requests that the Office of Management and Budget ("OMB") extend for an additional three years the current Paperwork Reduction Act ("PRA") clearance for information collection requirements contained in the Red Flags, Card Issuers, and Address Discrepancy Rules ("Rules"). That clearance expires on January 31, 2025.

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Compliance, Regulatory Requirement 7 Jan 2025 compliance, faa, class e airspace, aviation regulations, smith center

✈️Amendment of Class E Airspace for Smith Center, KS - 2024

This action amends the Class E airspace at Smith Center, KS. This action is the result of an airspace review conducted due to the decommissioning of the Mankato very high frequency omnidirectional range (VOR) as part of the VOR Minimum Operational Network (MON) Program. This action also updates the geographic coordinates of the airport to coincide with the FAA's aeronautical database. This action brings the airspace into compliance with FAA orders and supports instrument flight rule (IFR) procedures and operations.

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Compliance, Regulatory Requirements 7 Jan 2025 compliance, energy, natural gas, federal energy regulatory commission, rate filing, pipeline regulation
Compliance, Regulatory Requirements 7 Jan 2025 compliance, aviation, faa, gaylord mi, airspace regulation

✈️Amendment of Class E Airspace at Gaylord, MI by FAA

This action amends the Class E airspace at Gaylord, MI. This action is the result of an airspace review conducted due to the decommissioning of the Gaylord very high frequency omnidirectional range (VOR) as part of the VOR Minimum Operational Network (MON) Program. This action brings the airspace into compliance with FAA orders and supports instrument flight rule (IFR) procedures and operations.

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Regulatory Compliance 7 Jan 2025 compliance, information collection, department of justice, expungement form, fbi

📜DOJ Notice on FBI Expungement Form Information Collection Activities

The CJIS Division, FBI, DOJ, will be submitting the following information collection request to the Office of Management and Budget (OMB) for review and approval in accordance with the Paperwork Reduction Act of 1995.

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Regulatory Compliance, Environmental Regulations 7 Jan 2025 compliance, energy regulation, water quality certification, clean water act, northern states power
Compliance, Regulatory Guidance 7 Jan 2025 compliance, fda, biotechnology, genomic alterations, food animals

🧬FDA Guidance on Genomic Alterations in Food-Producing Animals

The Food and Drug Administration (FDA, Agency, or we) is announcing the availability of a draft guidance for industry (GFI) #251 entitled "Heritable Intentional Genomic Alterations in Animals of Food-Producing Species for Use as Models of Disease." This draft guidance, when finalized, will set forth FDA's policy regarding heritable intentional genomic alterations (IGAs) in animals of food- producing species, such as swine and rabbits, that are intended to be marketed for use as models of human or animal disease in biomedical research under contained and controlled conditions. The draft guidance describes the conditions under which we generally may not expect developers of IGAs in animal models of disease to submit an application to FDA's Center for Veterinary Medicine (CVM) or to get our approval before marketing their animals following CVM's prior review of risk factor data.

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