Oklahoma Amends Major Disaster Declaration Notice
The State of Oklahoma has amended its major disaster declaration notice, FEMA-4791-DR, dated June 14, 2024, due to Oklahoma.
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Florida Amendment No. 1 to Notice of a Major Disaster Declaration
The State of Florida has amended its major disaster declaration notice (FEMA-4794-DR), dated June 17, 2024, with Amendment No. 1.
Florida Amends Major Disaster Declaration Notice
The State of Florida has amended its major disaster declaration notice (FEMA-4794-DR) to update related determinations.
New Mexico Amendment to Major Disaster Declaration
This notice amends the June 20, 2024, major disaster declaration for New Mexico, FEMA-4795-DR, and related determinations.
Iowa Amendment 1 to Major Disaster Declaration
This notice amends the major disaster declaration for Iowa, originally declared on June 24, 2024, by FEMA.
Iowa Amendment No. 2 to Major Disaster Declaration
This notice amends the major disaster declaration for Iowa, originally declared on June 24, 2024, by FEMA.
Minnesota Amendment to Major Disaster Declaration
This notice amends the major disaster declaration for Minnesota, originally declared on June 28, 2024, by FEMA.
Texas Amendment No. 1 to Major Disaster Declaration
This notice amends the major disaster declaration for Texas, originally declared on July 9, 2024, by FEMA.
Texas Amendment No. 2 to Major Disaster Declaration
This notice amends the major disaster declaration for Texas, originally declared on July 9, 2024, by FEMA.
FAA Proposes Airworthiness Directive for MD Helicopters Helicopters
The FAA proposes a new airworthiness directive for certain MD Helicopters models due to a seized and damaged roller bearing in the pilot interconnecting cyclic torque tube assembly, requiring repetitive inspections and potential replacement or additional inspections.
FAA Proposes Airworthiness Directive for MHI RJ Aviation ULC Model CL-600-2B19 Airplanes
The FAA proposes a new airworthiness directive for MHI RJ Aviation ULC Model CL-600-2B19 airplanes due to potential cracks not detected by ultrasonic inspections, requiring repetitive inspections and repairs.
FAA Proposes Amendment to VOR Federal Airways in Eastern United States
The Federal Aviation Administration (FAA) is proposing to amend four domestic Very High Frequency Omnidirectional Range (VOR) Federal Airways in the eastern United States, primarily due to the planned decommissioning of the Roanoke, VA VOR/Distance Measuring Equipment (VOR/DME).
FAA Corrects RNAV Routes in Eastern United States
The Federal Aviation Administration (FAA) has corrected a final rule establishing three new RNAV Routes and amending three existing routes in the eastern United States to support the Next Generation Air Transportation System (NextGen).
Agency Receives Pesticide Petition for Residue Regulations
The US Agency has received a petition to establish or modify pesticide residue regulations for various commodities, as filed in June 2024.
EPA Proposes Rule to Address Unreasonable Risk of Injury from 1-Bromopropane (1-BP)
The Environmental Protection Agency (EPA) is proposing a rule to address the unreasonable risk of injury to human health from 1-bromopropane (1-BP), a widely used solvent, due to its significant adverse health effects, including neurotoxicity, developmental toxicity, and cancer.
Indoxacarb Pesticide Tolerances Established
The U.S. government has set tolerances for indoxacarb residues in multiple crops, following a request from Interregional Research Project Number 4 under the Federal Food, Drug, and Cosmetic Act.
EPA Exempts Ophioglossum pendulum IPD079Ea Protein from Tolerance Requirement for Corn
The US Environmental Protection Agency (EPA) has granted an exemption to Pioneer Hi-Bred International, Inc. from the requirement of a tolerance for residues of Ophioglossum pendulum IPD079Ea protein in corn, eliminating the need to establish a maximum permissible level for residues.
EPA Proposes Consent Decree to Address Lawsuit Over Air Quality Review
The Environmental Protection Agency (EPA) has proposed a consent decree to address a lawsuit filed by the Center for Biological Diversity, Sierra Club, and Center for Environmental Health, alleging the EPA failed to complete a review of air quality criteria and standards. The decree would establish deadlines for the EPA to take actions in its review.
Final Modifications to the Safer Choice Standard and a Provision for a Safer Choice Cleaning Service Certification Program; Notice of Availability
The Environmental Protection Agency (EPA) is announcing the availability of the final, updated Safer Choice and Design for the Environment (DfE) Standard, which includes changes to the Standard's title, packaging criteria, and certification for cleaning service providers. The update aims to help consumers and businesses find safer products for human health and the environment.
NRC Issues Final Environmental Assessment and Finding of No Significant Impact for Proposed Amendment to Three Mile Island Nuclear Station License
The U.S. Nuclear Regulatory Commission (NRC) has issued a final environmental assessment and finding of no significant impact for a proposed amendment to the license of the Three Mile Island Nuclear Station, Unit No. 2, allowing TMI-2 Energy Solutions to continue decommissioning the facility in accordance with NRC regulations.
FCC Proposes Handset Unlocking Requirements to Promote Consumer Choice and Wireless Competition
The Federal Communications Commission (FCC) is proposing a policy to require mobile wireless service providers to unlock handsets 60 days after activation, unless purchased through fraud.
FCC Approves Numbering Policies for Modern Communications for Three Years
The Wireline Competition Bureau announces that the Office of Management and Budget has approved the information collection associated with the Commission's revised Numbering Authorization Application rules for a period of three years. This approval is consistent with the FCC's Numbering Policies for Modern Communications, Second Report and Order (FCC 23-75).
Gray Television Licensee, LLC and SagamoreHill of Lubbock, LLC Seek Channel Swap at Lubbock, Texas
Gray Television Licensee, LLC and SagamoreHill of Lubbock, LLC have filed a joint petition with the Federal Communications Commission to swap channels 35 and 11 at Lubbock, Texas, allowing KCBD to operate on channel 35 and KJTV-TV to operate on channel 11.
FSA Amends Farm Loan Programs Regulations to Implement Distressed Borrower Set-Aside Program
The Farm Service Agency is introducing a new loan servicing program for financially distressed borrowers, allowing for loan installment deferral at a reduced interest rate, to improve access and delivery of farm loans and remove capital access barriers.
USDA Renews 47 Organic Substances, Completes 2025 Sunset Review
The US Department of Agriculture has renewed 47 substances listed on the National List of Allowed and Prohibited Substances, following the outcome of the 2025 sunset review processes and recommendations from the National Organic Standards Board.
ARS Seeks Extension of Information Collection for Document Delivery Services at NAL
The Agricultural Research Service (ARS) is requesting an extension of its currently approved information collection for document delivery services at the National Agricultural Library (NAL), set to expire on January 31, 2025.
USDA Rural Business-Cooperative Service Invites Applications for Intermediary Relending Program for FY 2025
The USDA Rural Development agency is seeking applications for the Intermediary Relending Program for fiscal year 2025, with funding subject to availability, and applicants are responsible for any expenses incurred in developing their application.
U.S. International Trade Commission Seeks Comments on Synthetic Braiding Hair Complaint
The U.S. International Trade Commission has received a complaint about Certain Pre-Stretched Synthetic Braiding Hair and Packaging Therefor, DN 3764, and is now soliciting public comments on any issues related to the public interest.
FDA Determines Regulatory Review Period for VANFLYTA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for the patent extension of VANFLYTA, a human drug product, following submissions to the US Patent and Trademark Office (USPTO).
FDA Determines Regulatory Review Period for REZLIDHIA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for REZLIDHIA, a human drug product, in response to a patent extension application submitted to the US Patent and Trademark Office (USPTO).
Flamingo Pharmaceuticals Ltd. Faces FDA Proposal to Withdraw Approval of Two ANDAs
The FDA is proposing to withdraw approval of two Abbreviated New Drug Applications (ANDAs) held by Flamingo Pharmaceuticals Ltd. due to repeated failure to file required annual reports, and is offering the company an opportunity to request a hearing on the proposal.
FDA Renews Blood Products Advisory Committee Charter for 2 Years
The Food and Drug Administration (FDA) has renewed the Blood Products Advisory Committee charter for an additional 2 years, with the new term set to expire on May 13, 2026, following a determination by the Commissioner of Food and Drugs that it is in the public interest to do so.
FDA Determines Regulatory Review Period for INPEFA Patent Extension
The U.S. Food and Drug Administration (FDA) has published a notice determining the regulatory review period for INPEFA, a pharmaceutical company, due to patent extension applications submitted to the U.S. Patent and Trademark Office (USPTO).
FDA Announces Experiential Learning Site Visit Program for Pharmaceutical Companies
The Food and Drug Administration (FDA) is inviting pharmaceutical companies to submit proposals to participate in its Fiscal Year 2025 Experiential Learning Site Visit Program, which aims to enhance quality and regulatory compliance in the industry.
FDA Announces Collection of Information for Food and Cosmetic Export Certificate Application Process Review
The Food and Drug Administration has submitted a proposed collection of information to the Office of Management and Budget for review and clearance, related to the application process for a food and cosmetic export certificate.
FDA Announces Public Meeting of Antimicrobial Drugs Advisory Committee for Sulopenem Etzadroxil/Probenecid Tablets
The FDA is hosting a public meeting of its Antimicrobial Drugs Advisory Committee to discuss a new drug application for Sulopenem Etzadroxil/Probenecid Tablets and is seeking public comments on the proposal.
FDA Determines Regulatory Review Period for TALZENNA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for the patent extension of TALZENNA, a human drug product, following a submission to the US Patent and Trademark Office (USPTO).
FDA Reopens Comment Period for Over-the-Counter Monograph M013
The US Food and Drug Administration is reopening the public comment period for a proposed rule to amend the regulation of over-the-counter pain relievers and anti-inflammatory medications, due to technical issues with the FDA's online portal, and is now accepting comments through the Federal eRulemaking portal.
FDA Requests Public Comment on Proposed Collection of Information for Healthcare Provider Survey
The Food and Drug Administration (FDA) is seeking public input on a proposed study to gather information from healthcare providers about prescription drug promotion, as required by the Paperwork Reduction Act of 1995.
FDA Determines Regulatory Review Period for XOFLUZA Patent Extension
The US Food and Drug Administration (FDA) has published a notice determining the regulatory review period for the patent extension of XOFLUZA, a human drug product, following a submission to the US Patent and Trademark Office (USPTO).
FDA Clears DELATESTRYL for Continued Sale
The US Food and Drug Administration (FDA) has ruled that DELATESTRYL (Testosterone Enanthate) Injection, 200 milligrams per milliliter, and other related drug products were not withdrawn from sale due to safety or effectiveness concerns, allowing them to continue being approved for use in abbreviated new drug applications (ANDAs).
FDA Withdraws Ciprofloxacin Hydrochloride Tablet from Sale Due to Safety Concerns
The US Food and Drug Administration has withdrawn Ciprofloxacin Hydrochloride tablet, equivalent to 100mg base, from sale due to concerns over its safety and effectiveness, and will not accept new applications for this medication.
Benuvia Operations, LLC. Seeks Registration as Controlled Substance Importer
Benuvia Operations, LLC. has submitted an application to the government to be authorized as an importer of controlled substances, a key step in the process of bringing these substances into the country.
Catalent Greenville, Inc. Applies to Register as Controlled Substance Importer
Catalent Greenville, Inc. has submitted an application to the authorities to be registered as an importer of controlled substances, a key step in the process of bringing these substances into the country.
U.S. Department of State Issues Certification Under Section 7045(a)(2)(A) of the Department of State, Foreign Operations, and Related Programs Appropriations Act, 2023
The U.S. Department of State has issued a certification under Section 7045(a)(2)(A) of the Department of State, Foreign Operations, and Related Programs Appropriations Act, 2023, which was signed into law on December 27, 2022
U.S. Passports Invalid for Travel to, in, or Through North Korea Until August 31, 2025
U.S. passports are currently invalid for travel to, in, or through North Korea, with the restriction set to expire on August 31, 2024, unless it is extended or revoked by the U.S. Secretary of State.
Company Announces Public Posting of Delegation of Authority Reports
The company has made its delegation of authority reports publicly available, as per the recently updated regulations
FinCEN Invites Comments on Proposed Renewal of Information Collection Requirements for Exempt Persons
FinCEN is seeking public comments on the proposed renewal of existing regulations requiring banks to file a FinCEN Form 110 to designate eligible customers as exempt persons, exempting them from reporting transactions over $10,000 in currency.
Department of Labor Requests Comments on New Information Collection for RESEA Evidence Building Portfolio Project
The Department of Labor is seeking public comment on a new information collection for the Reemployment Services and Eligibility Assessment (RESEA) Evidence Building Portfolio Project, as part of its effort to reduce paperwork and respondent burden.
Department of Labor Requests Comments on National Worker Survey Data Collection
The Department of Labor is seeking public input on its proposed National Worker Survey data collection, aiming to minimize respondent burden and ensure data quality, as part of its ongoing effort to reduce paperwork and improve the Paperwork Reduction Act of 1995 (PRA95) process.