Notice 25 Jun 2025 regulatory compliance, fda, patent extension, medical device, edwards lifesciences

🩺FDA Patent Extension Determination for EDWARDS SAPIEN 3 ULTRA RESILIA

The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for EDWARDS SAPIEN 3 ULTRA RESILIA premarket approval application (PMA) 140031 supplement (S-141) and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of applications to the Director of the U.S. Patent and Trademark Office (USPTO), Department of Commerce, for the extension of a patent which claims that medical device.

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Notice 25 Jun 2025 regulatory compliance, housing assistance, fema, disaster recovery, business opportunities

🏠Proposed FEMA Collection on Direct Housing Assistance Activities

The Federal Emergency Management Agency (FEMA), as part of its continuing effort to reduce paperwork and respondent burden, invites the general public to take this opportunity to comment on a revision of a currently approved information collection. In accordance with the Paperwork Reduction Act of 1995, this notice seeks comments concerning information collected by FEMA to provide temporary housing units, including manufactured housing units, recreational vehicles and other readily fabricated dwellings to eligible applicants who, as a direct result of a major disaster or emergency, are unable to occupy their primary residence or obtain adequate alternate housing, and therefore require temporary housing.

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Notice 25 Jun 2025 regulatory compliance, risk management, department of the interior, business liability, criminal enforcement

⚖️Guidance on Criminal Enforcement Regulations by Department of the Interior

This notice describes the Department of the Interior's ("Department" or "DOI") plans to address criminally liable regulatory offenses under the Executive Order 14294, "Fighting Overcriminalization in Federal Regulations."

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Notice 25 Jun 2025 regulatory compliance, information collection, public comments, general services administration, customer experience

🏛️GSA Seeks Public Comment for Information Collection on Services

The GSA, as part of its continuing effort to reduce paperwork and respondent burden, is announcing an opportunity for public comment on a proposed extension of a collection of information by the Agency. 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, and to allow 60 days for public comment in response to the notice. This notice solicits comments on an extension of an existing collection proposed by the Agency.

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Notice 25 Jun 2025 regulatory compliance, public hearing, business implications, cpsc, consumer safety, fiscal policy

🛡️CPSC Announces Public Hearing on Fiscal Years 2026 and 2027 Priorities

The U.S. Consumer Product Safety Commission (Commission or CPSC) will conduct a public hearing to receive views from interested parties about the Commission's agenda and priorities for fiscal year (FY) 2026, which begins on October 1, 2025, and for FY 2027, which begins on October 1, 2026. We invite members of the public to participate.

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Notice 25 Jun 2025 regulatory compliance, federal reserve, acquisitions, financial services, bank control

🏦Change in Bank Control Notices and Acquisition Applications

The Federal Reserve System announced changes regarding the Change in Bank Control Notices, detailing the acquisition process of shares in banks and bank holding companies. The public can inspect applications and submit comments, which are subject to disclosure, influencing regulatory outcomes and business strategies in the banking sector.

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Notice 25 Jun 2025 regulatory compliance, healthcare, fda, pharmaceutical, patent extension, filspari

💊FDA Notice on Regulatory Review Period for FILSPARI Patent Extension

The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for FILSPARI and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of an application to the Director of the U.S. Patent and Trademark Office (USPTO), Department of Commerce, for the extension of a patent which claims that human drug product.

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Notice 25 Jun 2025 regulatory compliance, healthcare, data collection, hrsa, transplant network, organ procurement

🏥Public Comment Request on Organ Procurement Data System Regulations

In compliance with the Paperwork Reduction Act of 1995, HRSA submitted an Information Collection Request (ICR) to the Office of Management and Budget (OMB) for review and approval. Comments submitted during the first public review of this ICR will be provided to OMB. OMB will accept further comments from the public during the review and approval period. OMB may act on HRSA's ICR only after the 30-day comment period for this notice has closed.

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Notice 25 Jun 2025 regulatory compliance, business operations, corporate filings, tariffs, energy sector, federal power act

⚡Combined Notice of Energy Filings and Compliance Requirements

The Department of Energy's notice includes details about electric corporate filings and compliance requirements from various applicants under the Federal Power Act. It cites important date deadlines for comments, emphasizes the need for interventions, and provides access to further filing details via the Commission's eLibrary system. Public participation is also encouraged in the regulatory process.

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Notice 25 Jun 2025 regulatory compliance, information collection, veterans affairs, educational institutions

📄Notice of Information Collection for Programs Abroad by VA

Veterans Benefits Administration, Department of Veterans Affairs (VA), is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act (PRA) of 1995, Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed revision of a currently approved collection, and allow 60 days for public comment in response to the notice.

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