🏺Notice of Intended Repatriation Under NAGPRA in Oregon
In accordance with the Native American Graves Protection and Repatriation Act (NAGPRA), the U.S. Department of the Interior, Bureau of Land Management, Oregon/Washington State Office, Lakeview District Office (BLM Lakeview District Office) intends to repatriate certain cultural items that meet the definition of unassociated funerary objects, sacred objects, and/or objects of cultural patrimony and that have a cultural affiliation with the Indian Tribes or Native Hawaiian organizations in this notice.
Learn More📊NSF Information Collection Activities Affecting Businesses
The National Science Foundation (NSF) has submitted the following information collection requirement to Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. This is the third notice for public comment; two 60-day notices were published in the Federal Register and ninety-five (95) comments from fourteen (14) individual sources were received. NSF is forwarding the proposed renewal submission to the OMB for clearance simultaneously with the publication of this notice.
Learn More🐾FDA Notice on New Animal Drug Information Collection Activities
The Food and Drug Administration (FDA, Agency, or we) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995.
Learn More📄OMB Review Notice
Under the provisions of the Paperwork Reduction Act, the Regulatory Secretariat Division has submitted to OMB a request to review and approve an extension of a previously approved information collection requirement regarding indirect cost rate proposals, payments to small business subcontractors, and bankruptcy notifications.
Learn More📡FCC Proposes Changes to Regulatory Fees for Fiscal Year 2025
In this document, the Federal Communications Commission (Commission) seeks comment on revising the fee schedule of FY 2025 regulatory fees and on several additional regulatory fee issues, as described in the text below.
Learn More💊FDA Notice on Regulatory Review and Patent Extension for BEYFORTUS
The Food and Drug Administration (FDA or the Agency) has determined the regulatory review period for BEYFORTUS 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 human biological product.
Learn More🌱Overview of Amendments to Genetically Engineered Organism Regulations
On December 2, 2024, a Federal court vacated the Animal and Plant Health Inspection Service (APHIS) final rule issued on May 18, 2020 (the May 2020 final rule) that revised APHIS' regulations governing the movement of certain genetically modified organisms and was issued under the authority of the Plant Protection Act. APHIS is therefore amending the CFR to conform the CFR to the Federal Court's vacatur of that rule. The Court's vacatur was effective December 2, 2024, and had the legal effect of vacating the May 2020 final rule in its entirety and restoring the legal effect of the pre-May 2020 regulations. These technical conforming amendments revise the CFR to reflect the court's vacatur of the May 2020 final rule.
Learn More📋DOL Seeks Comments on Income and Eligibility Verification System
The Department of Labor's (DOL) Employment and Training Administration (ETA) is soliciting comments concerning a proposed extension for the authority to conduct the information collection request (ICR) titled, "Income and Eligibility Verification System (IEVS) Confidentiality information collection request." This comment request is part of continuing Departmental efforts to reduce paperwork and respondent burden in accordance with the Paperwork Reduction Act of 1995 (PRA).
Learn More📦FDA Proposed Info Collection for Medical Device Exports
The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public comment on the proposed collection of certain 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, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on reporting requirements for firms that intend to export certain unapproved medical devices.
Learn More🧪CDC Proposes Data Collection on Thermal Spray Coating Health Risks
The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public burden and maximize the utility of government information, invites the general public and other federal agencies the opportunity to comment on a proposed information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Exposures, Health Effects, and Controls of Chemicals from Thermal Spray Coating: Part 2. The purpose of the proposed data collection is to assess exposures and respiratory health in workers using three thermal commonly used spray coating technologies and to investigate the association between exposures and respiratory health.
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