Latest changes
GovPing monitors 303 sources for this role across 4,036 total sources, covering Guidance, Enforcement, Rule, FAQ, Notice, and Consultation instruments. There were 872 changes in the last 7 days.
The New Jersey Optometry Board suspended Eric Robinson's license, while the FDA debarred Kimberly Schaff Kiehl for 10 years. Adam Brosius was sentenced to 24 months for a $33 million fraud scheme. Texas warned consumers not to eat Great Value Dino Nuggets due to lead contamination.
FDA Natural Family Planning Curricula Background Material
The FDA has posted background material related to Natural Family Planning curricula. This notice provides informational resources for interested parties.
FDA Document Details
The Food and Drug Administration (FDA) has published details for a new document on regulations.gov. This notice provides access to the document and its associated information for interested parties. Further details regarding the document's content are available via the provided URL.
FDA Proposes Pediatric Labeling Changes for ADHD Drugs
The FDA has issued a proposal to update the pediatric labeling for certain Attention Deficit Hyperactivity Disorder (ADHD) drugs. This consultation seeks public comment on the proposed changes to ensure accurate and up-to-date information for healthcare providers and patients regarding the use of these medications in children.
FDA Acknowledgment Letter to Irish Multimedia, LLC
The FDA has issued an acknowledgment letter to Irish Multimedia, LLC regarding a submission. The letter confirms receipt of the submission but provides no substantive details on its content or purpose.
Strattera Oral Solution SMPC Posting
The FDA has posted the Summary of Product Characteristics (SMPC) for Strattera oral solution on March 13, 2026. This posting provides updated information regarding the drug's characteristics and usage. It is intended for informational purposes for drug manufacturers and healthcare professionals.
FDA Acknowledgment Letter to North Bay Productions
The FDA's Division of Management and Budget (DMB) issued an acknowledgment letter to North Bay Productions on March 13, 2026. This notice confirms receipt of a submission from the company.
Osteopathic Family Physician Background Material
The FDA has posted background material related to Osteopathic Family Physicians. This notice provides informational content for stakeholders in the healthcare field.
FDA Document on Ovarian Cancer Risk Factors
The FDA has released a document concerning risk factors associated with ovarian cancer. This guidance is intended for manufacturers and healthcare providers involved in the pharmaceutical and medical device sectors.
FDA Natural Family Planning Review
The FDA has posted a review concerning Natural Family Planning methods. This document provides updated information and guidance related to these methods.
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 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.
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.
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.
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.
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.
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.
Importer of Controlled Substances Application: Purisys, LLC
Importer of Controlled Substances Application: Purisys, LLC
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 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.
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.
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.
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.
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.
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.
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.
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 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.
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.
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.
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 notices are published in the Federal Register to inform the public about scheduled meetings and their agendas.
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.
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 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.
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887 changes in last 7 days
Latest high priority updates
303 official sources tracked
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FDA warning letters, drug approvals, ICH guidelines, EMA updates, and DEA scheduling.
State commissioner bulletins, NAIC model laws, and DOI enforcement actions.
State AG privacy enforcement, FTC actions, CPPA rulemaking, and HIPAA enforcement.
Frequently asked questions
What does this feed cover?
CMS transmittals, MLN Matters articles, quality measure updates, HHS OIG work plan changes, HIPAA resolution agreements, Medicaid state plan amendments, and Joint Commission standard updates.
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Healthcare compliance officers, billing managers, and hospital administrators who need to track CMS and HHS changes that affect reimbursement, audits, and patient safety requirements.
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GovPing checks source pages multiple times daily.
Does this cover Medicaid state plan amendments?
Yes. We monitor CMS Medicaid pages and state plan amendment activity.
Why do CMS transmittals matter?
CMS transmittals change billing rules, coverage determinations, and reimbursement rates. Miss one and your organization could be billing incorrectly for months before an audit catches it.
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