Notice 2 Jun 2025 compliance, energy, regulation, federal energy regulatory commission, pacificorp, california independent system operator

⏳PacifiCorp Seeks Extension for Compliance with Order No. 881

PacifiCorp has filed a motion requesting an extension until October 15, 2027, to comply with the requirements of Order No. 881 and related regulations. This extension aims to address testing of vendor programs and operational readiness amid market integration concerns with the California Independent System Operator. Responses to the motion are due by June 17, 2025.

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Notice 2 Jun 2025 compliance, energy, regulation, environmental, public participation, licensing, hydroelectric, ketchikan

⚡Ketchikan Hydroelectric Project Licensing Notice and Public Input

The Department of Energy's Federal Energy Regulatory Commission has issued a notice regarding the licensing application for the Ketchikan Lakes Hydroelectric Project in Alaska. The document outlines the pre-filing process, solicits public comments, and describes upcoming scoping meetings and environmental assessments required under federal regulations. Interested stakeholders are invited to participate and share their feedback on the project.

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Notice 2 Jun 2025 compliance, regulation, aviation, faa, safety, unmanned aircraft

🛩️FAA Requires Safety Statements from Small Unmanned Aircraft Manufacturers

In accordance with the Paperwork Reduction Act of 1995, FAA invites public comments about our intention to request the Office of Management and Budget (OMB) approval to renew an information collection. The collection involves manufacturers of small unmanned aircraft providing a safety statement to owners of the UAS they produce. This is a statutory requirement. To minimize the burden on small businesses, the FAA has developed an example safety statement that can be used to satisfy the requirement. This FRN corrects the previously submitted 60-day FRN to include updated contact information and docket number.

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Notice 2 Jun 2025 regulation, business operations, pharmaceuticals, foreign-trade zones, michigan

💊Proposed Production in Foreign-Trade Zone 189 for Pharmaceutical Products

The Department of Commerce has issued a notice regarding a proposed production activity by Grand River Aseptic Manufacturing within Foreign-Trade Zone 189 in Michigan, concerning the production of nivolumab and its active ingredient, atigotatug. Public comments are invited and will influence the approval process.

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Notice 30 May 2025 compliance, regulation, logistics, shipping, maritime, federal

🚢FMC Plans to Revoke Exemptions for Controlled Carriers

The Federal Maritime Commission ("Commission") intends to revoke certain exemptions that had been granted to some controlled carriers, allowing for their rates, charges, classifications, rules or regulations to become effective with less than thirty (30) days' notice. This revocation would apply to exemptions that were granted to entities that have since been removed from the Commission's list of controlled carriers. Exemptions that have been granted to controlled carriers that remain on this list would continue to be valid but may be reviewed in the future. The Commission invites comments from the public on this proposed action.

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Proposed Rule 30 May 2025 compliance, healthcare, regulation, telecommunications, fcc, aerospace

📡FCC Petition for Reconsideration

Petitions for Reconsideration (Petition) have been filed in the Commission's proceeding by Kara R. Curtis on behalf of Aerospace and Flight Test Radio Coordinating Council, Inc. and by Ari Q. Fitzgerald et al. on behalf of GE HealthCare Technologies Inc.

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Notice 30 May 2025 compliance, regulation, fda, manufacturing, drug products, color additives

🎨FDA Guidance on Replacing Color Additives in Drug Products

The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance for industry entitled "Replacing Color Additives in Approved or Marketed Drug Products." This draft guidance provides recommendations for replacing color additives in approved or marketed drug products. If a color additive is replaced in a drug product, information to support the change should be retained and available at the manufacturing facility. Additionally, this draft guidance recommends that new drug application (NDA) and abbreviated new drug application (ANDA) holders submit information to support color additive replacements in changes being effected in 30 days (CBE-30) supplements. Although a qualitative or quantitative change to an inactive ingredient is generally considered a major change, in many cases, replacing a color additive with one that is listed in the color additive regulations is unlikely to adversely affect the identity, strength, quality, purity, or potency of the drug product. Therefore, this draft guidance recommends a CBE-30 for such a change.

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Proposed Rule 30 May 2025 compliance, regulation, transportation, motor carriers, safety, alcohol abuse, drug abuse, federal, highway safety, commercial motor vehicles

🚦Proposed Regulation on Railroad Grade Crossings for CMVs

FMCSA proposes to amend the regulations related to driving a commercial motor vehicle (CMV) at railroad grade crossings. Currently, drivers of certain CMVs (e.g., buses transporting passengers and CMVs transporting certain hazardous materials) are required to stop before crossing a railroad track unless an exception applies, such as when the crossing is controlled by a functioning highway traffic signal transmitting a green indication. The Agency proposes to add a similar exception for a railroad grade crossing equipped with an active warning device that is not in an activated state (e.g., flashing lights or crossing gates down, indicating the arrival of a train).

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Notice 30 May 2025 healthcare, cms, information collection, regulation, business compliance, esrd

📋CMS Seeks Comments on Agency 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 a second opportunity for public comment on the notice. Interested persons are invited to send comments regarding the burden estimate 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.

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Notice 30 May 2025 compliance, agriculture, usda, regulation, foreign investment, afida

🌾Revised Agricultural Foreign Investment Disclosure Act Information Collection

In accordance with the Paperwork Reduction Act requirement, the Farm Service Agency (FSA) is requesting comments from all interested individuals and organizations on a revision of a currently approved information collection request associated with the Agricultural Foreign Investment Disclosure Act of 1978 (AFIDA). This revised form is the basis for the development of a streamlined process for electronic submission and retention of AFIDA disclosures, which is required by the Consolidated Appropriations Act, 2023. Foreign persons, as defined by AFIDA, who are making amendments to existing filings, or filing land or leasehold dispositions, will continue to use the existing form as those filings are on paper.

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