FSIS Proposed Rule on Poultry Line Speed Rates
The Food Safety and Inspection Service (FSIS) is proposing to amend regulations concerning poultry slaughter establishments. The proposed changes would increase line speeds for young chicken and turkey establishments and clarify inspection procedures, while also removing requirements for annual worker safety attestations. Comments are due by April 20, 2026.
FSIS Nutrition Labeling of Meat and Poultry - Notice and Comment
The Food Safety and Inspection Service (FSIS) has issued a notice requesting comments on the renewal of an approved information collection regarding nutrition labeling for raw meat and poultry products. The existing collection, which has no proposed changes, is set to expire on July 31, 2026.
FSIS Proposed Rule on Swine Slaughter Line Speeds
The Food Safety and Inspection Service (FSIS) is proposing to amend regulations to allow swine slaughter establishments to determine their own line speeds, provided they maintain process control. FSIS also proposes to clarify inspector authority to reduce line speeds and remove the annual worker condition attestation requirement. Comments are due by April 20, 2026.
CDC Performance Measures Project Consultation
The Centers for Disease Control and Prevention (CDC) is seeking public comment on its Performance Measures Project. The comment period for this consultation closes on April 27th.
CDC Notice on Questionnaire Design and Evaluation Research
The Centers for Disease Control and Prevention (CDC) has issued a notice regarding research on questionnaire design and evaluation. This notice outlines the CDC's interest in advancing best practices for developing and assessing survey instruments used in public health research.
CDC Meeting Notice and Request for Comment on Immunization Practices
The CDC has issued a notice for a meeting of the Advisory Committee on Immunization Practices (ACIP) to be held on March 18-19, 2026. The notice also includes a request for written comments, which were due by March 12, 2026. The meeting agenda includes discussions on COVID-19 vaccine injuries and Long-COVID.
CDC Notice on Improving National Health and Nutrition Examination Survey Programs
The Centers for Disease Control and Prevention (CDC) has issued a notice regarding improvements to the National Health and Nutrition Examination Survey (NHANES) programs. This notice outlines updates and enhancements aimed at refining data collection and survey methodologies.
CDC Notice on Cognitive Testing with Comment Period
The CDC has issued a notice regarding cognitive testing, opening a comment period that closes on May 8. This consultation seeks input on proposed changes or new requirements related to cognitive assessment protocols.
CMS Medicare Part C/D Reporting Requirements Notice Comment Period
The Centers for Medicare & Medicaid Services (CMS) is seeking public comment on its intention to collect information related to Medicare Part C and D reporting requirements. This notice provides a 60-day comment period for interested parties to submit feedback on the proposed information collection.
Medicare Advantage Deeming Authority Renewal for NCQA
The Centers for Medicare & Medicaid Services (CMS) is considering the renewal of the National Committee for Quality Assurance's (NCQA) Medicare Advantage deeming authority. This notice requests public comments on whether to approve NCQA's application to continue deeming Health Maintenance Organizations and Preferred Provider Organizations compliant with certain Medicare requirements.
Medicare/Medicaid CY 2026 Payment Policies Correction Notice
The Centers for Medicare & Medicaid Services (CMS) issued a correction notice for the CY 2026 Physician Fee Schedule final rule. This notice corrects typographical and technical errors in the original rule, which finalized payment policies for Medicare and Medicaid programs for calendar year 2026.
CMS Seeks Public Comment on Information Collection Activities
The Centers for Medicare & Medicaid Services (CMS) is seeking public comment on its intention to collect information from the public under the Paperwork Reduction Act. This notice provides an opportunity for interested parties to submit comments on the proposed information collection activities.
Error Document Not Found
A general error occurred while processing a request on regulations.gov, indicating that the document or docket could not be found. Users are advised to check the URL or return to the homepage.
Public Health Service Rule Withdrawal
The Public Health Service has withdrawn a previously issued rule. This action removes the rule from the Code of Federal Regulations. Further details on the specific rule withdrawn are not provided in the document title.
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The regulations.gov website is displaying an error page indicating that a requested document could not be found. Users are advised that the link may be outdated or incorrect, and they should try returning to the homepage or contacting the Help Desk if the problem persists.
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Regulations.gov Document Not Found Error
Regulations.gov is experiencing a technical error, preventing access to documents. Users are advised to check the URL, return to the homepage, or contact the Help Desk if the problem persists. The specific document referenced by the URL could not be found.
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An error occurred on regulations.gov, and the requested document could not be found. The website suggests the link may be outdated or incorrect. Users are advised to try the URL again or contact the Help Desk if the problem persists.
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A general error occurred while processing a request on regulations.gov, indicating that the requested document could not be found. Users are advised to check the URL or return to the homepage.
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The US Federal Government website regulations.gov is experiencing an error, indicating that a requested document could not be found. Users are advised that the link may be outdated or incorrect, and they should try the URL again or contact the Help Desk if the problem persists.
ONDCP Senior Executive Service Performance Review Board Appointments
The Office of National Drug Control Policy (ONDCP) has announced the appointment of four individuals to its Senior Executive Service Performance Review Board. The notice, published on February 28, 2025, identifies the Chair and other members of this board.
Website Error - Document Not Found
A general error occurred on the regulations.gov website, indicating that the requested document could not be found. Users are advised to check the URL, return to the homepage, or contact the Help Desk if the problem persists.
OSHRC Performance Review Board Member Appointments
The Occupational Safety and Health Review Commission (OSHRC) has issued an annual notice announcing the appointment of members to its Senior Executive Service Performance Review Board (PRB). The PRB is responsible for reviewing and evaluating senior executive performance appraisals and making recommendations on ratings and awards.
OSHRC Notice: Modified Privacy Act Systems of Records
The Occupational Safety and Health Review Commission (OSHRC) has issued a notice of modified Privacy Act systems of records. These revisions aim to clarify record access, contesting, and notification procedures and update citations. The changes become effective on October 8, 2025.
OSHRC Performance Review Board Membership Notice
The Occupational Safety and Health Review Commission (OSHRC) has issued an annual notice announcing the appointment of members to its Performance Review Board (PRB). The PRB is responsible for reviewing senior executive performance appraisals and making recommendations on ratings and awards.
OSHRC Performance Review Board Member Appointment Notice
The Occupational Safety and Health Review Commission (OSHRC) has issued an annual notice announcing the appointment of members to its Performance Review Board (PRB). The PRB is responsible for reviewing and evaluating senior executive performance appraisals and making recommendations on ratings, awards, and pay adjustments.
OSHRC Withdraws Notice on Performance Review Board Members
The Occupational Safety and Health Review Commission (OSHRC) is withdrawing a previously published notice regarding the appointment of members to its Performance Review Board. This action is in compliance with a Presidential Executive Order on restoring accountability for career senior executives.
Monoject Syringe Recall - Incorrect Insulin Labeling
Health Canada has issued a recall for Monoject 1mL Luer Lock Syringes due to incorrect insulin labeling. The outer packaging indicates a tuberculin syringe, but the syringes inside are U-100 insulin syringes. Healthcare providers are advised to contact the manufacturer for more information.
Instinct Plus Endoscopic Clipping Device Recalled Due to Malfunctions
Health Canada has issued a Type II recall for the Instinct® Plus Endoscopic Clipping Device manufactured by Wilson-Cook Medical, Inc. due to malfunctions where the clip may remain attached to the drive wire and cannot be opened. This recall affects products manufactured prior to corrective actions being implemented.
Arjo Tenor Mobile Lift Recall
Health Canada has issued a Type II recall for the Arjo Tenor Mobile Lift due to a defect in the brake component of the actuator. The defect can cause a loss of self-locking and uncontrolled descent, posing a safety risk. Affected units must be removed from use immediately.
SOLTIVE Laser System Recall
Health Canada has issued a Type II recall for the SOLTIVE Premium SuperPulsed Laser System due to a defect in the 24V power supply causing sudden power loss. Affected healthcare providers should contact the manufacturer for service coordination.
IHS 2026 Reimbursement Rates Notice
The Indian Health Service (IHS) has published a notice regarding the 2026 reimbursement rates. This notice provides updated financial information for healthcare providers participating in IHS programs.
Indian Health Service Expands Purchased/Referred Care Delivery Area for Iowa Tribe
The Indian Health Service (IHS) has expanded the Purchased/Referred Care Delivery Area (PRCDA) for the Iowa Tribe of Kansas and Nebraska. This expansion adds Jackson County, Kansas, and Holt County, Missouri, to the existing service area, aiming to authorize additional tribal members to receive Purchased/Referred Care services.
Indian Health Service CHEF Threshold for FY25 Set at $19,095
The Indian Health Service (IHS) has announced the Catastrophic Health Emergency Fund (CHEF) threshold for Fiscal Year 2025. The threshold has been set at $19,095, reflecting a 0.5% increase from the previous year's medical care expenditure category of the Consumer Price Index.
IHS Announces FY2026 Catastrophic Health Emergency Fund Threshold
The Indian Health Service (IHS) announced the Catastrophic Health Emergency Fund (CHEF) threshold for Fiscal Year 2026. The threshold has been set at $19,630, an increase from the previous year, calculated based on medical care expenditure inflation.
Indian Health Service Employment Declaration Form Public Comment
The Indian Health Service (IHS) is requesting public comments on the reinstatement of the "Addendum to Declaration for Federal Employment (OF 306), Indian Health Service, Childcare and Indian Child Care Worker Positions" form. This notice is part of the Paperwork Reduction Act process, seeking input on an existing information collection.
HHS Proposed Rule: HIV Organ Transplant Policy Equity Act Implementation
The Department of Health and Human Services (HHS) proposes to amend regulations implementing the National Organ Transplant Act (NOTA) to remove research and Institutional Review Board (IRB) requirements for the transplantation of kidneys and livers from HIV-positive donors to HIV-positive recipients. This proposed rule aligns with the HIV Organ Policy Equity (HOPE) Act.
HRSA Document HRSA-2026-0001-0001
The Health Resources and Services Administration (HRSA) has issued a new government document, identified as HRSA-2026-0001-0001. This notice serves as an informational update for healthcare providers and public health authorities within the United States.
HRSA Notice 2026-03838
The Health Resources and Services Administration (HRSA) has issued Notice 2026-03838. This notice provides general information and updates relevant to healthcare providers and public health authorities. Specific details regarding the content of the notice are available via the provided URL.
HRSA Announces 340B Rebate Model Pilot Program Application Process
The HRSA announced the application process for a voluntary 340B Rebate Model Pilot Program for qualifying drug manufacturers. The agency is also requesting public comment on the program's structure and application process, with a deadline of September 8, 2025.
HOPE Act Final Regulatory Impact Analysis
The Health Resources and Services Administration (HRSA) has published the final Regulatory Impact Analysis (RIA) for the HOPE Act. This document details the anticipated costs and benefits associated with the implementation of the HOPE Act.
ECHA Publications: PFAS Opinions and Biocidal Products Committee Highlights
ECHA has published new updates including opinions on a PFAS restriction proposal from its Risk Assessment Committee and Socio-Economic Analysis Committee. Additionally, highlights from the February Biocidal Products Committee meeting are available, detailing adopted opinions on active substances and authorisations.
Importer of Controlled Substances Application: Purisys, LLC
Importer of Controlled Substances Application: Purisys, LLC
Pest Risk Analysis for Sweet Potato Imports from South Korea
The Animal and Plant Health Inspection Service (APHIS) has issued a notice of availability for a pest risk analysis concerning the importation of fresh sweet potato roots from the Republic of Korea into the United States. The agency is seeking public comment on the analysis, which evaluates potential phytosanitary measures.
APHIS Adds Sri Lanka to African Swine Fever Affected Regions List
The Animal and Plant Health Inspection Service (APHIS) has added Sri Lanka to its list of regions affected by African Swine Fever (ASF). This action, effective December 4, 2024, imposes import restrictions on pork and pork products from Sri Lanka to prevent the introduction of ASF into the United States.
APHIS Brucellosis Eradication Program Information Collection Revision
The Animal and Plant Health Inspection Service (APHIS) is requesting a revision and extension of approval for an information collection related to the Cooperative State-Federal Brucellosis Eradication Program. This notice is part of the public comment period for the proposed changes.
APHIS Notice: Pioneer Hi-Bred Maize Risk Assessment Extension
The Animal and Plant Health Inspection Service (APHIS) has received a request from Pioneer Hi-Bred International, Inc. to extend a determination of nonregulated status for a new variety of genetically engineered maize (DP51291) based on its similarity to a previously approved variety (DP23211). APHIS is making this extension request and its draft risk assessment available for public comment.
APHIS Extension Request
The Animal and Plant Health Inspection Service (APHIS) has posted a request for an extension related to a previous notice. This action concerns a specific docket number and is part of ongoing regulatory processes.
AHRQ Information Collection Proposal: Research Reporting System
The Agency for Healthcare Research and Quality (AHRQ) has announced its intention to seek OMB approval for the AHRQ Research Reporting System (ARRS). This notice provides a 60-day period for public comment on the proposed information collection project.
HHS Interpretation of Federal Public Benefit under PRWORA
The Department of Health and Human Services (HHS) has issued a notice to clarify its interpretation of 'Federal public benefit' under the Personal Responsibility and Work Opportunity Reconciliation Act of 1996 (PRWORA). This notice revises a prior interpretation and identifies HHS programs that provide federal public benefits, with a 30-day comment period.
HHS Request for Information on Deregulation
The U.S. Department of Health and Human Services (HHS) has issued a Request for Information (RFI) to solicit public input on potential deregulation efforts. This initiative aims to reduce regulatory burdens across all areas touched by HHS, in line with presidential directives. Comments are due by July 14, 2025.
PRWORA Notice RIA from AHRQ
The Agency for Healthcare Research and Quality (AHRQ) has posted a Regulatory Impact Analysis (RIA) notice related to the Personal Responsibility and Work Opportunity Reconciliation Act (PRWORA). This notice provides information regarding the analysis conducted by the agency.
ATSDR Notice 2025-23599
The Agency for Toxic Substances and Disease Registry (ATSDR) issued a notice regarding a public comment period that concluded on February 23, 2026. This notice pertains to a specific document identified by ATSDR-2025-23599. Further details on the subject matter are available via the provided URL.
ATSDR Extends Comment Period for Draft Toxicological Profiles
The Agency for Toxic Substances and Disease Registry (ATSDR) has extended the public comment period for five draft toxicological profiles. The deadline for submitting comments has been moved to February 13, 2025.
ATSDR Tox Profile for Benzene
The Agency for Toxic Substances and Disease Registry (ATSDR) has posted a final toxicological profile for Benzene. This document provides comprehensive health information on the substance, intended for public health and healthcare professionals.
ATSDR Tox Profile for CDDs
The Agency for Toxic Substances and Disease Registry (ATSDR) has posted a Toxicological Profile for CDDs. This document provides health information concerning environmental agents and is intended for public health and environmental professionals.
ATSDR Tox Profile for Carbon Disulfide
The Agency for Toxic Substances and Disease Registry (ATSDR) has posted a Toxicological Profile for Carbon Disulfide. This document provides health information concerning exposure to this chemical.
Sunshine Act Meeting Notice from Federal Register
Sunshine Act Meeting Notice from Federal Register
Sunshine Act Meeting notice published January 20, 2004
Sunshine Act Meeting notice published January 20, 2004
Uniformed Services University Board of Regents meeting announced
Uniformed Services University Board of Regents meeting announced
HHS Certified Laboratories for Drug Testing
The Department of Health and Human Services (HHS) has published an updated list of certified laboratories and instrumented initial testing facilities that meet minimum standards for urine and oral fluid drug testing for federal agencies. This notice provides the current list of approved facilities.
SAMHSA Agency Information Collection Activities: Program Evaluation for Prevention Contract
The Substance Abuse and Mental Health Services Administration (SAMHSA) is requesting OMB review and public comment on a revision to its Program Evaluation for Prevention Contract (PEPC) data collection activities. This revision seeks to extend data collection through FY 2028 for the Strategic Prevention Framework for Prescription Drugs (SPF Rx) program.
Reagan-Udall Foundation: Steering Committee Nominations
The Reagan-Udall Foundation for the Food and Drug Administration is requesting nominations for its Steering Committee. Interested parties must submit nominations by September 4, 2015. The Foundation's Board of Directors will select the committee members.
Reagan-Udall Foundation Scientific Advisory Committee Nominations
The Reagan-Udall Foundation for the Food and Drug Administration is requesting nominations for its Scientific Advisory Committee. Interested individuals must submit their nominations by May 24, 2015.
Reagan-Udall Foundation: Steering Committee Nominations
The Reagan-Udall Foundation for the Food and Drug Administration is requesting nominations for its PredicTox Steering Committee. Interested parties must submit nominations by August 28, 2015.
Reagan-Udall Foundation Seeks Steering Committee Nominations
The Reagan-Udall Foundation for the Food and Drug Administration is seeking nominations for its PredicTox Steering Committee. Nominations must be submitted by August 28, 2015, with selected members to be notified by September 30.
Reagan-Udall Foundation Annual Public Meeting Notice
The Reagan-Udall Foundation for the Food and Drug Administration has announced its annual public meeting. The notice provides details on the meeting date, time, and registration deadlines for attendees and those wishing to make oral presentations.
FDA Delays Effective Date for Statutory Evaluations
The Food and Drug Administration (FDA) has issued a correction to delay the effective date for certain statutory evaluations. This administrative delay affects rules published under the Department of Health and Human Services and its various agencies.
Approval of Respiratory Protective Devices
The Public Health Service, through the Department of Health and Human Services, has issued a final rule regarding the approval of respiratory protective devices. This rule is published in the Federal Register and pertains to specific regulations within 42 CFR 84.
FDA Proposal to Withdraw or Repeal Statutory Evaluations
The Food and Drug Administration, along with other HHS agencies, has proposed to withdraw or repeal certain statutory evaluations. This action is part of an effort to secure updated and necessary evaluations. The proposal is open for public comment.
Administrative Delay of Statutory Evaluations Effective Date
The Department of Health and Human Services, through multiple agencies including FDA, CMS, and ACF, has issued a final rule to administratively delay the effective date of certain statutory evaluations. This rule impacts the implementation timeline for these evaluations, providing additional administrative time.
Withdrawing Rule on Securing Updated Statutory Evaluations
The Department of Health and Human Services, through multiple agencies including FDA and CMS, has withdrawn a final rule concerning the timely securing of updated statutory evaluations. This withdrawal action removes the previously established requirements related to these evaluations.
ONDCP Appointment of Senior Executive Service Performance Review Board Members
The Office of National Drug Control Policy (ONDCP) has published a notice announcing the appointment of four individuals to its Senior Executive Service Performance Review Board. The notice identifies Ms. Michele Marx as Chair, along with Ms. Debbie Seguin, Ms. Shannon Kelly, and Mr. Kemp Chester as members.
Appointment of Senior Executive Service Performance Review Board members
The Office of National Drug Control Policy has published a notice announcing the appointment of members to its Senior Executive Service Performance Review Board. This notice serves to inform the public of these appointments.
Privacy Act of 1974; System of Records Notice
The Office of National Drug Control Policy (ONDCP) has published a notice establishing a new system of records, "Correspondence Management systems (CMS) for the Office of National Drug Control Policy (ONDCP), ONDCP/001." This system will track correspondence received, sent, or referred to the ONDCP.
High Intensity Drug Trafficking Areas Designation
The Office of National Drug Control Policy has designated five new areas as High Intensity Drug Trafficking Areas (HIDTA). This designation aims to enhance federal, state, and local law enforcement efforts to combat drug trafficking in these specific regions.
Appointment of Senior Executive Service Performance Review Board Members
The Office of National Drug Control Policy has published a notice announcing the appointment of members to its Senior Executive Service Performance Review Board. This action is part of the agency's internal administrative processes for evaluating executive performance.
Senior Executive Service Performance Review Board Membership
The Occupational Safety and Health Review Commission has published a notice detailing the membership of its Senior Executive Service Performance Review Board. This notice, effective March 28, 2025, outlines the composition of the board responsible for performance reviews within the SES.
Occupational Safety and Health Review Commission Senior Executive Service Performance Review Board Membership
The Occupational Safety and Health Review Commission has announced the membership of its Senior Executive Service Performance Review Board. This notice details the individuals appointed to this board, effective February 19, 2025.
Privacy Act of 1974 System of Records Modifications
The Occupational Safety and Health Review Commission (OSHRC) is revising its Privacy Act system of records notices. These modifications aim to provide clarity, update citations, and reflect changes in record-keeping related to federal employee leave and telework.
Senior Executive Service Performance Review Board Membership
The Occupational Safety and Health Review Commission has issued a notice regarding the membership of its Senior Executive Service Performance Review Board. This notice specifies the effective date for the membership, which is January 16, 2026.
OSHA: FM Approvals LLC Recognition Expansion and Test Standards Modification
The Occupational Safety and Health Administration (OSHA) has published a notice regarding FM Approvals LLC. This notice details an expansion of FM Approvals LLC's recognition and modifications to the list of appropriate test standards under the Nationally Recognized Testing Laboratory (NRTL) Program. The changes are effective March 11, 2026.
OSHA: TUV Rheinland Inc. Expansion of Recognition Granted
The Occupational Safety and Health Administration (OSHA) has granted an expansion of recognition to TUV Rheinland of North America, Inc. This notice details the updated scope of recognition for the accredited testing laboratory.
Bay Area Compliance Laboratories Expansion of Recognition
The Occupational Safety and Health Administration (OSHA) has granted an expansion of recognition to Bay Area Compliance Laboratories. This notice details the expanded scope of recognition for the laboratory.
Center for Scientific Review Notice of Closed Meetings
The National Institutes of Health (NIH) Center for Scientific Review has issued a notice regarding upcoming closed meetings. These meetings are scheduled for April 13-14, 2026, and are part of the review process for grant applications.
Office of the Secretary Cancellation of Meeting
The National Institutes of Health, through the Office of the Secretary, has issued a notice cancelling a previously scheduled meeting. The notice was published in the Federal Register on March 16, 2026.
National Bipartisan Commission on Future of Medicare Public Meeting Notice
The National Bipartisan Commission on the Future of Medicare published a notice announcing a public meeting. This notice serves as an informational update regarding the commission's activities.
National Bipartisan Commission on Future of Medicare Public Meeting Notice
The National Bipartisan Commission on the Future of Medicare has announced a public meeting. This notice serves to inform interested parties about the upcoming meeting and its purpose related to the future of Medicare.
National Bipartisan Commission on Future of Medicare Public Meeting Notice
The National Bipartisan Commission on the Future of Medicare has announced a public meeting. This notice provides details for interested parties to attend and participate in discussions regarding the future of Medicare.
Public Meeting Announced by National Bipartisan Commission on Future of Medicare
The National Bipartisan Commission on the Future of Medicare announced a public meeting. This notice serves to inform the public about the upcoming meeting, providing details for participation.
National Bipartisan Commission on Future of Medicare Public Meeting Notice
The National Bipartisan Commission on the Future of Medicare announced a public meeting through a notice published in the Federal Register. This notice serves to inform interested parties about the upcoming meeting details.
Petition for Modification of Mandatory Safety Standards
The Mine Safety and Health Administration (MSHA) has published a notice regarding a petition for modification of existing mandatory safety standards. The notice provides a comment period for interested parties to submit their views on the petition.
MSHA Address Update Technical Amendment
The Mine Safety and Health Administration (MSHA) has published a technical amendment to update its address and contact information. This rule affects various sections of the Code of Federal Regulations related to mining safety and health.
MSHA Proposed Extension of Information Collection for Slope and Shaft Sinking Plans
The Mine Safety and Health Administration (MSHA) is proposing to extend an existing information collection requirement regarding slope and shaft sinking plans for underground coal mines. This notice is open for public comment.
Proposed Extension of Information Collection: Mine Rescue Teams
The Mine Safety and Health Administration (MSHA) is proposing to extend an existing information collection regarding mine rescue teams. This includes arrangements for emergency medical assistance and transportation for injured persons, as well as reporting and posting requirements. The public comment period for this proposal ends on March 27, 2026.
Petition to Modify Application of Safety Standards - MSHA
The Mine Safety and Health Administration (MSHA) has published a notice regarding a petition to modify the application of existing mandatory safety standards. The public has until February 11, 2026, to submit comments on the petition.
Medicare Payment Advisory Commission Meeting Notice
The Medicare Payment Advisory Commission (MedPAC) announced a public meeting scheduled for September 8-9, 2005. The notice provides details on the meeting's purpose and agenda, inviting public participation.
Medicare Payment Advisory Commission Meeting Notice
The Medicare Payment Advisory Commission (MedPAC) announced a public meeting scheduled for December 9-10, 2004. The notice provides details on the meeting's purpose and agenda, allowing interested parties to attend or observe.
Medicare Payment Advisory Commission Meeting Notice
The Medicare Payment Advisory Commission (MedPAC) has issued a notice announcing a public meeting scheduled for January 12-13, 2005. The meeting will cover various topics related to Medicare payments and policy.
Medicare Payment Advisory Commission Meeting Notice
The Medicare Payment Advisory Commission (MedPAC) has announced a public meeting scheduled for March 10-11, 2005. The notice provides details on the meeting's agenda and location for interested parties.
Commission Meeting Announcement
The Medicare Payment Advisory Commission announced a public meeting scheduled for April 21-22, 2005. The notice provides details on the meeting agenda and location.
Health Care Programs: Fraud and Abuse Exclusion Authorities Revisions
The Office of Inspector General (OIG) at HHS has issued a proposed rule to revise its fraud and abuse exclusion authorities. This proposed rule aims to update the criteria and processes by which individuals and entities can be excluded from participating in Federal health care programs.
HHS OIG Delays Effective Date of Rule Consistent With Moratorium
The Department of Health and Human Services Office of Inspector General (HHS OIG) has delayed the effective date of certain provisions within 42 CFR 1001.952(h) and (cc). This action aligns with a congressionally enacted moratorium, impacting specific healthcare arrangements.
Performance Standards for Medicaid Fraud Control Units
The Office of Inspector General (OIG) within the Department of Health and Human Services has issued final performance standards for Medicaid Fraud Control Units (MFCUs). These standards, effective upon publication, aim to enhance the effectiveness of MFCUs in combating Medicaid fraud, waste, and abuse.
HHS OIG Solicitation for Safe Harbors and Fraud Alerts
The Department of Health and Human Services Office of Inspector General (HHS OIG) is soliciting proposals for new and modified safe harbors and special fraud alerts under the Medicare fraud and abuse provisions. This action aims to update existing protections and identify new areas of concern for healthcare providers.
Medicare Fraud and Abuse: Request for Information on Anti-Kickback Statute
The Office of the Inspector General for the Health and Human Services Department has issued a Request for Information regarding the Federal Anti-Kickback Statute and Beneficiary Inducements Civil Monetary Penalties. This consultation seeks public input on potential updates and clarifications to existing fraud and abuse provisions.
Indian Health Service Reimbursement Rates for Calendar Year 2026
The Indian Health Service has published the reimbursement rates for calendar year 2026. This notice provides the updated per diem rates for inpatient hospital services, excluding physician and practitioner services, for the upcoming year.
Notice of Purchased/Referred Care Delivery Area Redesignation for Iowa Tribe
The Indian Health Service has issued a notice redesignating the Purchased/Referred Care Delivery Area for the Iowa Tribe of Kansas and Nebraska. This change is effective as of the publication date. The notice details the specific geographic areas affected by this redesignation.
Public Comment Sought on Federal Employment Information Collection
The Indian Health Service is seeking public comment on a proposed information collection related to the Declaration for Federal Employment (OF 306) form. This notice is part of the standard public comment period for new or revised information collections.
Catastrophic Health Emergency Fund (CHEF) Threshold Announced
The Indian Health Service, part of the Department of Health and Human Services, has announced the threshold for the Catastrophic Health Emergency Fund (CHEF). This notice provides specific details regarding the fund's operational parameters.
Catastrophic Health Emergency Fund 2026 Threshold Announced
The Indian Health Service has announced the threshold for the Catastrophic Health Emergency Fund (CHEF) for Fiscal Year 2026. This notice provides the specific financial threshold that will be in effect for the upcoming fiscal year.
Health Workforce Connector Public Comment Request
The Health Resources and Services Administration has submitted a revision to the Health Workforce Connector information collection activity to the Office of Management and Budget (OMB) for review and approval. The public has 32 days to submit comments on this submission.
NIH Director's Office Meeting Notice
The National Institutes of Health (NIH) has published a notice announcing an upcoming meeting of the Office of the Director. The notice provides details regarding the meeting, which is scheduled for April 13, 2026. This is an informational announcement regarding a government meeting.
Center for Scientific Review Notice of Closed Meetings
The National Institutes of Health's Center for Scientific Review has announced upcoming closed meetings. These meetings are scheduled to occur on April 14, 2026. The purpose of these meetings is related to the review of grant applications.
Center for Scientific Review Closed Meetings Notice
The National Institutes of Health published a notice regarding upcoming closed meetings for the Center for Scientific Review. These meetings are scheduled for April 15, 2026, and will involve discussions that are exempt from public disclosure under specific provisions of the Government in the Sunshine Act.
HRSA Ryan White HIV/AIDS Program Part F Public Comment Request
The Health Resources and Services Administration (HRSA) is requesting public comment on proposed information collection activities related to the HRSA Ryan White HIV/AIDS Program Part F National AIDS Education and Training Center Program. The comment period closes on April 8, 2026.
Agency Information Collection Activities: Public Comment Request
The Health Resources and Services Administration (HRSA) has submitted a revision to the Ryan White HIV/AIDS Program Part F Dental Services Report for OMB review and approval. A public comment period is open until March 30, 2026.
Public Comment Request for Standardized Work Plan Form
The Health Resources and Services Administration is requesting public comment on a proposed standardized work plan form for use with applications for research and training grants and cooperative agreements. The comment period closes on May 5, 2026.
Maternal, Infant, Early Childhood Home Visiting Program Data Collection
The Health Resources and Services Administration (HRSA) has submitted a request to the Office of Management and Budget (OMB) for continued approval of the Maternal, Infant, and Early Childhood Home Visiting Program Performance Measurement Information System. This revision consolidates data collection forms and aims to reduce administrative burden and align with current guidelines.
SCHIP Funds Redistribution and Availability for FY 1999
The Health Care Financing Administration issued a notice regarding the redistribution and continued availability of unexpended State Children's Health Insurance Program (SCHIP) funds for Fiscal Year 1999. This notice clarifies the allocation and use of these funds for states.
Agency Information Collection Activities: Proposed Collection; Comment Request
The Health Care Financing Administration (HCFA) has published a notice requesting public comment on proposed agency information collection activities. This notice is part of the standard process for reviewing and approving information collection requests under the Paperwork Reduction Act.
Medicare and Medicaid Programs; Solicitation of PACE Proposals
The Health Care Financing Administration (HCFA) has issued a notice soliciting proposals for a private, for-profit demonstration project for the Program of All-Inclusive Care for the Elderly (PACE). Interested organizations can begin submitting letters of intent on August 10, 2001, and full proposals starting December 10, 2001.
Agency Information Collection Activities: OMB Review Comment Request
The Health Care Financing Administration (HCFA) submitted agency information collection activities for review and comment by the Office of Management and Budget (OMB). This notice requests public input on these collections.
Information Collection Activities; Proposed Collection; Comment Request
The Department of Health and Human Services, through the Agency for Healthcare Research and Quality, has issued a notice requesting public comment on proposed information collection activities. The comment period closes on July 15, 2013.
WIC Breastfeeding Award of Excellence Collection Comment Request
The Food and Nutrition Service has published a proposed collection of information regarding the Special Supplemental Nutrition Program for Women, Infants and Children (WIC) Breastfeeding Award of Excellence. The public has until May 11, 2026, to submit comments.
OMB Clearance for Annual Survey of School Food Authorities
The Food and Nutrition Service has issued a notice regarding the Office of Management and Budget's (OMB) generic clearance for the annual survey of school food authorities. This notice is open for public comment until March 24, 2026.
Summer Food Service Program 2026 Reimbursement Rates
The Department of Agriculture's Food and Nutrition Service has published the 2026 reimbursement rates for the Summer Food Service Program. These rates are applicable from January 1, 2026, and provide updated financial guidelines for program operators.
SNAP Agency Information Collection for Interstate Data Matching
The Food and Nutrition Service (FNS) has issued a notice regarding a proposed agency information collection activity for the Supplemental Nutrition Assistance Program (SNAP). This activity concerns a requirement for interstate data matching to prevent multiple issuances of benefits.
SNAP Trafficking Controls and Fraud Investigations Document
The Food and Nutrition Service has issued a notice regarding agency information collection activities related to Supplemental Nutrition Assistance Program (SNAP) trafficking controls and fraud investigations, specifically concerning card replacement. The notice includes a public comment period.
Animal Food and Egg Regulatory Program Standards Comment Request
The Food and Drug Administration (FDA) is requesting public comments on proposed information collection activities related to Animal Food and Egg Regulatory Program Standards. The comment period is open for 30 days.
Medical Devices for Weight Loss: Premarket Considerations Guidance
The Food and Drug Administration (FDA) has published new guidance for industry and FDA staff regarding premarket considerations for medical devices indicated for weight loss. This guidance aims to clarify regulatory pathways and expectations for manufacturers seeking approval for such devices.
FDA - Investigational New Drug Application Requirements Collection
The Food and Drug Administration (FDA) is proposing to collect information related to Investigational New Drug (IND) application requirements. This notice opens a public comment period for stakeholders to provide input on the proposed information collection activities.
FDA Mammography Standards Quality Act Requirements - OMB Review
The Food and Drug Administration (FDA) has submitted a request for Office of Management and Budget (OMB) review regarding information collection activities related to the Mammography Standards Quality Act Requirements. This notice opens a 30-day public comment period.
FDA Withdraws Proposed Rule on Sunlamp Products
The Food and Drug Administration (FDA) has withdrawn a previously proposed rule concerning the restricted sale, distribution, and use of sunlamp products. This action removes the proposed regulations that were initially published in 2015.
FSIS Request to Renew Information Collection: Sanitation SOPs, HACCP
The Food Safety and Inspection Service (FSIS) has requested to renew an approved information collection regarding Sanitation Standard Operating Procedures (SOPs) and Hazard Analysis and Critical Control Point (HACCP) systems. This notice is open for public comment for 30 days.
FSIS 2026 Rate Changes for Inspection and Laboratory Services
The Food Safety and Inspection Service (FSIS) is announcing its 2026 rates for voluntary, overtime, and holiday inspection, laboratory services, and export application fees. Most rates will remain the same as 2025, with a reduction in laboratory service rates effective January 11, 2026.
Poultry Inspection System Line Speed Rates for Chicken and Turkey
The Food Safety and Inspection Service (FSIS) has proposed new maximum line speed rates for young chicken and turkey establishments operating under the New Poultry Inspection System. This proposed rule aims to update current operational standards for poultry processing facilities.
Swine Slaughter Inspection System: Maximum Line Speed
The Food Safety and Inspection Service has issued a proposed rule to establish the maximum line speed for the new Swine Slaughter Inspection System (NSIS). This proposal is open for public comment until April 20, 2026.
FSIS Request to Renew Nutrition Labeling Information Collection
The Food Safety and Inspection Service (FSIS) has published a notice requesting to renew an approved information collection regarding nutrition labeling for major cuts of single-ingredient raw meat or poultry products and ground or chopped meat and poultry products. The public has 58 days to submit comments.
Sunshine Act Meetings Notice
The Federal Mine Safety and Health Review Commission has issued a notice regarding an upcoming Sunshine Act meeting. The meeting is scheduled for April 15, 2026, at 10 a.m. This notice serves to inform the public about the meeting's time, date, place, and matters to be considered.
Sunshine Act Meetings Announced by Federal Mine Safety and Health Review Commission
The Federal Mine Safety and Health Review Commission has announced upcoming Sunshine Act meetings. These meetings are scheduled for March 5, 2026, and will cover specific matters to be considered by the commission.
Federal Mine Safety Commission Procedural Rules Correction
The Federal Mine Safety and Health Review Commission has issued a correction to its procedural rules. This document clarifies existing regulations and does not introduce new obligations.
Sunshine Act Meetings by Federal Mine Safety Commission
The Federal Mine Safety and Health Review Commission has issued a notice regarding upcoming Sunshine Act meetings. The notice specifies the date, time, and location for a meeting scheduled for March 26, 2026, detailing the matters to be considered.
Sunshine Act Meetings announced by Federal Mine Safety and Health Review Commission
The Federal Mine Safety and Health Review Commission has announced upcoming Sunshine Act meetings. These notices are published in the Federal Register to inform the public about scheduled meetings and their agendas.
CMS Agency Information Collection Activities Proposed Collection Comment Request
The Centers for Medicare & Medicaid Services (CMS) is requesting public comment on its intention to collect information from the public. This notice is part of the process required by the Paperwork Reduction Act of 1995. The comment period closes on May 11, 2026.
Medicare Program Deeming Authority Renewal for NCQA
The Centers for Medicare & Medicaid Services (CMS) has issued a notice regarding the renewal of deeming authority for the National Committee for Quality Assurance (NCQA). This notice is open for public comment until April 9, 2026.
CMS Approves Rural Health Clinic Accreditation Program
The Centers for Medicare & Medicaid Services (CMS) has approved the American Association for Accreditation of Ambulatory Surgery Facilities' (AAAASF) Rural Health Clinic (RHC) accreditation program. This approval allows AAAASF to accredit RHCs for Medicare and Medicaid participation.
CMS Agency Information Collection Activities Proposed Collection Comment Request
The Centers for Medicare & Medicaid Services (CMS) has published a notice requesting public comment on proposed information collection activities. The comment period is open until May 11, 2026.
Proposed Data Collection for Public Comment
The Centers for Disease Control and Prevention (CDC) has submitted a proposed data collection for public comment. The comment period for this proposed collection ends on May 8, 2026. This action is part of the CDC's ongoing efforts to gather information for public health initiatives.
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has published a notice regarding agency forms undergoing review under the Paperwork Reduction Act. This notice initiates a 30-day review period for specific forms to assess their information collection requirements.
Proposed Data Collection for Public Comment
The Centers for Disease Control and Prevention (CDC) has submitted a proposed data collection for public comment. The comment period closes on May 8, 2026. This notice initiates a consultation period for a new data collection initiative.
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has published a notice regarding agency forms undergoing review under the Paperwork Reduction Act. This notice initiates a 30-day review period for public comment on the forms.
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has published a notice regarding agency forms undergoing review under the Paperwork Reduction Act. This notice initiates a 30-day review period for specific forms to assess their continued necessity and burden on respondents.
Pioneer Hi-Bred maize genetically engineered status assessment
The Animal and Plant Health Inspection Service (APHIS) has published a notice regarding Pioneer Hi-Bred International, Inc.'s request for an extension of determination of nonregulated status for genetically engineered maize. The notice includes a plant pest risk similarity assessment and is open for public comment.
Proposed Revision to US Import Requirements for Pineapples from Taiwan
The Animal and Plant Health Inspection Service (APHIS) has proposed revisions to the import requirements for pineapples from Taiwan into the United States. This notice is open for public comment until May 4, 2026.
Addition of Sri Lanka to African Swine Fever Affected Regions List
The Animal and Plant Health Inspection Service (APHIS) has added Sri Lanka to its list of regions affected by African Swine Fever (ASF). This notice updates the agency's official list of regions considered to be affected by the disease.
Notice of Availability of Pest Risk Analysis for Sweet Potato Importation from Korea
The Animal and Plant Health Inspection Service (APHIS) has issued a notice regarding the availability of a Pest Risk Analysis (PRA) for the importation of fresh sweet potato roots from the Republic of Korea into the United States. A public comment period is open for 59 days.
Agency Forms Undergoing Paperwork Reduction Act Review
The Agency for Toxic Substances and Disease Registry has submitted forms for review under the Paperwork Reduction Act. This notice informs the public about the agency's intent to collect information and allows for public comment on the necessity and burden of these forms.
Availability of Five Draft Toxicological Profiles
The Agency for Toxic Substances and Disease Registry (ATSDR) has made five draft toxicological profiles available for public comment. These profiles address potential health risks associated with various substances. Comments are due by February 6, 2025.
Agency Forms Undergoing Paperwork Reduction Act Review
The Agency for Toxic Substances and Disease Registry (ATSDR) has published a notice regarding agency forms undergoing review under the Paperwork Reduction Act. This notice informs the public about the forms that are subject to review and potential revision.
Availability of Draft Toxicological Profiles; Comment Period Extended
The Agency for Toxic Substances and Disease Registry (ATSDR) has extended the public comment period for five draft toxicological profiles. The original notice was published on November 8, 2024, and the new deadline for comments is February 13, 2025.
Proposed Data Collection for Public Comment
The Agency for Toxic Substances and Disease Registry (ATSDR) is proposing a new data collection and is seeking public comment. The comment period closes on February 20, 2026.
Patient Safety Organizations: Voluntary Relinquishment for Vizient PSO
The Agency for Healthcare Research and Quality (AHRQ) has published a notice delisting the Vizient TM PSO (PSO number P0007) from its list of Patient Safety Organizations. This action is effective January 7, 2026, following the PSO's voluntary relinquishment of its status.
Agency Information Collection Activities: Proposed Collection Comment Request
The Federal Register is requesting public comment on a proposed collection of information by a government agency. The document indicates a server error and is not currently accessible.
Agency Information Collection Activities Proposed Collection Comment Request
The Agency for Healthcare Research and Quality (AHRQ) has published a notice requesting public comment on proposed information collection activities. This notice outlines the specific data collection efforts for which AHRQ is seeking input from stakeholders.
Patient Safety Organizations: Expired Listing for MedExpress PSO
The Agency for Healthcare Research and Quality (AHRQ) has issued a notice regarding the expired listing of MedExpress PSO as a Patient Safety Organization. This notice serves to inform the public and relevant parties of this administrative change.
Agency Information Collection Activities: Proposed Collection; Comment Request
The Agency for Healthcare Research and Quality (AHRQ) has published a notice requesting public comment on proposed new agency information collection activities. The comment period is open until April 10, 2026.
FDA Approves Wellcovorin for Cerebral Folate Deficiency
The FDA has approved Wellcovorin (leucovorin calcium) tablets for the treatment of cerebral folate deficiency in adult and pediatric patients with a confirmed FOLR1 gene variant. This marks the first FDA-approved treatment for this rare genetic condition.
FDA Approves Tec-Dara for Relapsed Multiple Myeloma
The FDA has approved Tec-Dara (teclistamab and daratumumab hyaluronidase-fihj) for relapsed or refractory multiple myeloma. This approval was granted under the Commissioner's National Priority Voucher (CNPV) pilot program, marking a significant acceleration in the review process.
FDA Meeting on State Drug Importation Program
The FDA held a meeting with several states to discuss the Section 804 Importation Program (SIP), which allows states to import certain prescription drugs from Canada. This meeting is part of the FDA's implementation of an executive order aimed at lowering drug prices for American consumers.
FDA Streamlines Biosimilar Development Guidance
The FDA issued draft guidance to streamline biosimilar development by recommending the reduction of unnecessary clinical pharmacokinetic testing when scientifically justified. This initiative aims to save developers up to 50% in PK study costs, potentially lowering drug prices and increasing patient access to affordable biologic treatments.
FDA Launches Unified Adverse Event Analysis Platform AEMS
The FDA has launched a new unified platform, the Adverse Event Monitoring System (AEMS), to analyze adverse event reports for all regulated products. This modernization aims to improve data accessibility, transparency, and surveillance capabilities, replacing fragmented legacy systems and is expected to save $120 million over five years.
USDA FSIS Public Health Alert for Turkey Pastry Products
The USDA's Food Safety and Inspection Service (FSIS) has issued a public health alert for frozen, ready-to-eat turkey stuffed pastry products due to misbranding and undeclared allergens. The affected products may contain milk, a known allergen, which is not declared on the product labels. Consumers are advised not to consume these products.
Ajinomoto Foods Recalls Fried Rice, Ramen, and Shu Mai
Ajinomoto Foods North America Inc. is recalling approximately 3,900 pounds of fried rice, ramen, and shu mai products due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide. Consumers are advised not to consume these products.
Medicare Drug Price Negotiation: Manufacturer Participation in Third Cycle
CMS announced that 15 drug manufacturers have chosen to participate in the third cycle of Medicare drug price negotiations. These negotiations, part of the Inflation Reduction Act, will determine prices for selected high-expenditure drugs, with negotiated prices effective beginning in 2028.
MHRA Guidance on Medicine Reclassification for Improved Access
The MHRA has published guidance discussing the potential benefits of reclassifying medicines to improve patient access to treatments and reduce pressure on NHS services. The guidance highlights opportunities for self-care and innovation within the consumer healthcare sector.