Last Updated
Jan 22, 2026, 15:11 PM
Department of State
30-Day Notice of Proposed Information Collection: Medical Examination for Visa or Immigration Benefit
The
Department of State has submitted the information collection on medical
examination for visa or immigration benefit to the Office of Management
and Budget (OMB) for approval. Forms for this collection are completed
by panel physicians on behalf of aliens seeking a visa; refugees;
refugees and asylees (including following-to-join); and certain
parolees. The forms record the medical information necessary to
determine whether an alien has a medical or other condition affecting
his or her eligibility for a visa or immigration benefit. The
information requested includes the result of any diagnostic tests
required for the diagnosis of diseases identified as communicable
diseases of public health significance, as well as other evaluations
identified as necessary to confirm a medical ineligibility or to comply
with other requirements. Collecting this information is essential to
protecting public health in the United States.
Comment Period: Submit comments up to January 22, 2026.
Federal Register: 30-Day Notice of Proposed Information Collection: Medical Examination for Visa or Immigration Benefit
Centers for Medicare & Medicaid Services
Medicare and Medicaid Programs; Repeal of Minimum Staffing Standards for Long-Term Care Facilities
This
interim final rule with comment period repeals provisions of the final
rule titled “Medicare and Medicaid Programs; Minimum Staffing Standards
for Long-Term Care Facilities and Medicaid Institutional Payment
Transparency Reporting.” This action is taken in view of changes made by
public law, which precludes HHS from implementing, administering, or
enforcing certain provisions of the final rule until September 30, 2034.
Effective Date: These regulations are effective on February 2, 2026.
Comment Period: To be assured consideration, comments must be received at one of the addresses provided below, by February 2, 2026.
Federal Register: Medicare and Medicaid Programs; Repeal of Minimum Staffing Standards for Long-Term Care Facilities
Food and Drug Administration (FDA) and Department of Health and Human Services (HHS)
Increasing Access to Nonprescription Drugs; Request for Information
The
FDA is announcing a request for information from interested parties and
the public to share their perspectives with FDA on how to increase
access to nonprescription drugs. The FDA intends to use the information
submitted to inform plans for a public meeting intended to be held in
calendar year 2026.
Comment Period: Either electronic or written comments on the notice must be submitted by February 2, 2026.
Federal Register: Increasing Access to Nonprescription Drugs; Request for Information.
Health Resources and Services Administration(HRSA)
Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; COVID-19 Provider Relief Fund and American Rescue Plan Rural Payment Reporting Activities, OMB No. 0906-0068-Revision
HRSA disbursed the COVID-19 Provider
Relief Fund (PRF) and American Rescue Plan (ARP) Rural payments to
eligible health care providers to support health care-related expenses
or lost revenues attributable to the COVID-19 pandemic. Recipients of
PRF and ARP Rural payments agreed to a set of Terms and Conditions
(T&C), which, among other requirements, mandate compliance with
certain reporting requirements that facilitate appropriate oversight of
recipients' use of funds. Providers who have attested to the T&Cs
regarding their PRF and ARP Rural payment(s), including the requirement
that the provider will use the HRSA Consolidated PRF Reporting Portal to
submit information about their use of PRF and ARP Rural payments. There
will be one new Data Form Element, the Repayment ID, which is generated
by HRSA and provided in the email giving the recipient the opportunity
to report, and it will be entered by the provider in the HRSA
Consolidated PRF Reporting Portal. Approximately 50 data elements will
be removed from the PRF and ARP Rural Reporting Portal, including
sections on personnel, patient, and facility metrics as well as survey
questions on the PRF program.
Comment Period: Comments on this ICR should be received no later than February 6, 2026.
Department of Health and Human Services (HHS)
Solicitation of Proposals for New and Modified Safe Harbors and Special Fraud Alerts
In
accordance with section 205 of the Health Insurance Portability and
Accountability Act of 1996 (HIPAA), this annual notification solicits
proposals and recommendations for developing new, or modifying existing,
safe harbor provisions under section 1128B(b) of the Social Security
Act (the Act), the Federal anti-kickback statute, as well as developing
new OIG Special Fraud Alerts.
Comment Period: To ensure consideration, public comments must be received no later than 5 p.m. on February 9, 2026.
Federal Register: Solicitation of Proposals for New and Modified Safe Harbors and Special Fraud Alerts.
Department of Health and Human Services (HHS)
Agency Information Collection Request; 30-Day Public Comment Request
Office
for Civil Rights (OCR) is requesting Office of Management and Budget
(OMB) approval for a new information collection. Under OCR's delegated
civil enforcement authority, a person may file a complaint with OCR for
alleged noncompliance with 42 CFR part 2
(“Part 2”). OCR will collect information from individuals using the
form, Confidentiality of Substance Use Disorder Patient Records
Complaint, to allow OCR to collect the minimum information needed from
individuals who file complaints with OCR to form the basis for the
initial processing of such complaints to satisfy the right of an
individual to file a complaint.
Comment Period: Comments on the Information Collection Request (ICR) must be received on or before February 12, 2026.
Federal Register: Agency Information Collection Request; 30-Day Public Comment Request
Centers for Medicare & Medicaid Services
Medicare and Medicaid Programs; Hospital Condition of Participation: Prohibiting Sex-Rejecting Procedures for Children
This
proposed rule would revise the requirements that Medicare and Medicaid
certified hospitals must meet to participate in the Medicare and
Medicaid programs. These changes are necessary to protect the health and
safety of children and reflect HHS' review of recent information on the
safety and efficacy of sex-rejecting procedures (SRPs) on children. The
revisions to the requirements would prohibit hospitals from performing
sex-rejecting procedures on children.
Comment Period: To be assured consideration, comments must be received at one of the addresses provided in the notice, no later than 5 p.m. on February 17, 2026.
Federal Register: Medicare and Medicaid Programs; Hospital Condition of Participation: Prohibiting Sex-Rejecting Procedures for Children
Centers for Medicare & Medicaid Services
Medicaid Program; Prohibition on Federal Medicaid and Children's Health Insurance Program Funding for Sex-Rejecting Procedures Furnished to Children
This proposed rule would require that a State
Medicaid plan must provide that the Medicaid agency will not make
payment under the plan for sex-rejecting procedures for children under
18 and prohibit the use of Federal Medicaid dollars to fund
sex-rejecting procedures for individuals under the age of 18. In
addition, it would require that a separate State Children's Health
Insurance Program (CHIP) plan must provide that the CHIP agency will not
make payment under the plan for sex-rejecting procedures for children
under 19 and prohibit the use of Federal CHIP dollars to fund
sex-rejecting procedures for individuals under the age of 19.
Comment Period: To be assured consideration, comments must be received at one of the addresses provided in the notice, no later than 5 p.m. on February 17, 2026.
Federal Register: Medicaid Program; Prohibition on Federal Medicaid and Children's Health Insurance Program Funding for Sex-Rejecting Procedures Furnished to Children
Department of Health and Human Services
Request for Information: Accelerating the Adoption and Use of Artificial Intelligence as Part of Clinical Care
The
HHS Office of the Deputy Secretary in collaboration with ASTP/ONC has
published this Request for Information (RFI) to seek broad public
comment on what HHS can do to accelerate the adoption and use of AI as
part of clinical care.
Comment
Period: To be assured consideration, written or electronic comments
must be received at one of the addresses provided in the notice, by February 23, 2026.
Federal Register: Request for Information: Accelerating the Adoption and Use of Artificial Intelligence as Part of Clinical Care
Centers for Medicare & Medicaid Services
Guarding U.S. Medicare Against Rising Drug Costs (GUARD) Model
This
proposed rule would implement the Guarding U.S. Medicare Against Rising
Drug Costs (GUARD) Model to test a new Medicare payment model under
section 1115A of the Social Security Act. The model proposes a test of
an alternative payment method for calculating inflation rebates for
certain Part D drugs and biological products. The proposed GUARD Model
would test whether changing the calculation of the Part D inflation
rebate would reduce costs for the Medicare program while preserving or
enhancing quality of care for Part D enrollees.
Comment Period: To be assured consideration, comments must be received at one of the addresses provided in the notice, by February 23, 2026.
Federal Register: Guarding U.S. Medicare Against Rising Drug Costs (GUARD) Model
Centers for Medicare & Medicaid Services
Global Benchmark for Efficient Drug Pricing (GLOBE) Model
This
proposed rule proposes to implement the Global Benchmark for Efficient
Drug Pricing Model (“GLOBE Model”), a new Medicare payment model under
section 1115A of the Social Security Act (the Act). The GLOBE Model
would test whether a payment model that uses an alternative method for
calculating Part B inflation rebate amounts for certain separately
payable Part B drugs and biologicals products reduces costs for Medicare
fee-for-service (FFS) beneficiaries and the Medicare program while
preserving quality of care.
Comment Period: To be assured consideration, comments must be received at one of the addresses provided in the notice, by February 23, 2026.
Federal Register: Global Benchmark for Efficient Drug Pricing (GLOBE) Model
Department of Health and Human Services
Health Data, Technology, and Interoperability: ASTP/ONC Deregulatory Actions To Unleash Prosperity
This
proposed rule focuses on deregulatory actions identified in HHS
regulations regarding Health information technology standards,
implementation specifications, and certification criteria and
certification programs for health information technology, and
information blocking. This proposed rule seeks to reduce burden, offer
flexibility to both developers and providers, and support innovation
through the removal and revisions of certain certification criteria and
regulatory provisions. This proposed rule also seeks to address reported
misuse and abuse of information blocking definitions and exceptions.
Comment
Period: To be assured consideration, written or electronic comments
must be received at one of the addresses provided in the notice, no later than 5 p.m. Eastern Time on February 27, 2026.
Federal Register: Health Data, Technology, and Interoperability: ASTP/ONC Deregulatory Actions To Unleash Prosperity