Notice2026-10934

Agency Information Collection Activities: Submission for OMB Review; Comment Request

Primary source

Metadata and text below are from the Federal Register, a public-domain U.S. government work. Always verify the official published version before relying on it for any legal matter.

Published
June 2, 2026

Issuing agencies

Health and Human Services DepartmentCenters for Medicare & Medicaid Services

Abstract

The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS' intention to collect information from the public. 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 or reinstatement of an existing collection of information, and to allow a second opportunity for public comment on the notice. Interested persons are invited to send comments regarding the burden estimate or any other aspect of this collection of information, including the necessity and utility of the proposed information collection for the proper performance of the agency's functions, the accuracy of the estimated burden, ways to enhance the quality, utility, and clarity of the information to be collected, and the use of automated collection techniques or other forms of information technology to minimize the information collection burden.

Full Text

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<title>Federal Register, Volume 91 Issue 105 (Tuesday, June 2, 2026)</title>
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[Federal Register Volume 91, Number 105 (Tuesday, June 2, 2026)]
[Notices]
[Pages 32978-32979]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2026-10934]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10463 and CMS-10492]


Agency Information Collection Activities: Submission for OMB 
Review; Comment Request

AGENCY: Centers for Medicare & Medicaid Services, Health and Human 
Services (HHS).

ACTION: Notice.

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SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is 
announcing an opportunity for the public to comment on CMS' intention 
to collect information from the public. 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 or reinstatement of an 
existing collection of information, and to allow a second opportunity 
for public

[[Page 32979]]

comment on the notice. Interested persons are invited to send comments 
regarding the burden estimate or any other aspect of this collection of 
information, including the necessity and utility of the proposed 
information collection for the proper performance of the agency's 
functions, the accuracy of the estimated burden, ways to enhance the 
quality, utility, and clarity of the information to be collected, and 
the use of automated collection techniques or other forms of 
information technology to minimize the information collection burden.

DATES: Comments on the collection(s) of information must be received by 
the OMB desk officer by July 2, 2026.

ADDRESSES: Written comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to <a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a>. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
    To obtain copies of a supporting statement and any related forms 
for the proposed collection(s) summarized in this notice, please access 
the CMS PRA website by copying and pasting the following web address 
into your web browser: <a href="https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing">https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing</a>.

FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.

SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 
(PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from 
the Office of Management and Budget (OMB) for each collection of 
information they conduct or sponsor. The term ``collection of 
information'' is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and 
includes agency requests or requirements that members of the public 
submit reports, keep records, or provide information to a third party. 
Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires 
federal agencies to publish a 30-day notice in the Federal Register 
concerning each proposed collection of information, including each 
proposed extension or reinstatement of an existing collection of 
information, before submitting the collection to OMB for approval. To 
comply with this requirement, CMS is publishing this notice that 
summarizes the following proposed collection(s) of information for 
public comment.

Information Collection

    Type of Information Collection Request: Reinstatement with change 
of a previously approved collection; Title of Information Collection: 
Cooperative Agreement to Support Navigators in Federally-facilitated 
Exchanges and State Partnership Exchanges; Use: Section 1311(i) of the 
ACA requires Exchanges to establish a Navigator program under which it 
awards grants to eligible individuals and entities, as described in 
Section 1311(i)(2) of the ACA and 45 CFR 155.210(a) and (c), to carry 
out certain Navigator duties in states with an FFE. Entities or 
individuals that receive a cooperative agreement award must be capable 
of carrying out, at a minimum, all Navigator duties required by the ACA 
and HHS regulations. The primary regulations that establish 
requirements for Navigator grant awardees are 45 CFR 155.210 and 
155.215. Under the terms and conditions of the Navigator program 
cooperative agreements, awardees must provide progress reports on a 
weekly, monthly, and quarterly basis, and a final report at the end of 
the five-year period of performance. Form Number: CMS-10463 (OMB 
control number: 0938-1215); Frequency: Annually, Monthly, Quarterly, 
Weekly; Affected Public: Private Sector; Businesses or other for-
profits, Not-for-profit institutions; Number of Respondents: 44; Total 
Annual Responses: 120,236; Total Annual Hours: 457,857. (For questions 
regarding this collection contact Gian Johnson at 301-492-4323.)
    2. Type of Information Collection Request: Revision of a currently 
approved collection; Title of Information Collection: Coverage of 
Certain Preventive Services Under the Affordable Care Act: Data 
Submission Requirements to Receive the Federally-facilitated Exchange 
User Fee Adjustment; Use: The Patient Protection and Affordable Care 
Act, Public Law 111-148, enacted on March 23, 2010, and the Health Care 
and Education Reconciliation Act, Public Law 111-152, enacted on March 
30, 2010 [collectively, the ``Affordable Care Act'' (ACA)], provides 
the authority for the U.S. Department of Health and Human Services 
(HHS) to charge user fees to issuers participating in Federally-
facilitated Exchanges (FFEs) and State-based Exchanges on the Federal 
platform (SBE-FPs). Additionally, section 2713 of the Public Health 
Service Act (PHS Act) requires coverage without cost sharing of certain 
preventive health services, including certain contraceptive services, 
in non-exempt, non-grandfathered group health plans and health 
insurance coverage, including issuers participating in the FFEs and 
SBE-FPs. The final rule ``Coverage of Certain Preventive Services Under 
the Affordable Care Act'' (78 FR 39870) set forth regulations regarding 
coverage for certain preventive services under section 2713 of the PHS 
Act. The final regulations (78 FR 39870) establish rules under which 
the third party administrator (TPA) of a self-insured group health plan 
will provide or arrange for a third party to provide separate 
contraceptive coverage to plan participants and beneficiaries without 
cost sharing, premium, fee, or other charge to plan participants or 
beneficiaries or to the eligible organization or its plan under a 
process to accommodate qualifying objections to contraceptive coverage.
    The final rules (78 FR 39870) also require the submission of 
certain information to HHS and the associated adjustment of user fees 
to issuers, as well as standards to fund the payments for the 
contraceptive services that are provided for participants and 
beneficiaries in self-insured plans of eligible organizations under the 
accommodation described previously, through an adjustment to the user 
fees payable by issuers. HHS requires this information to ensure that 
these FFE (or SBE-FP) user fee adjustments reflect payments for 
contraceptive services provided under this accommodation and that the 
adjustment is applied to the appropriate participating issuer.
    This document describes the data collection requirements related to 
this adjustment, collected via a webform. This revision includes a 
decrease in burden, with the total estimated issuer and TPA burden and 
associated costs decreasing based on past years of experience with the 
program demonstrating a decreasing number of participants. Form Number: 
CMS-10492 (OMB Control Number: 0938-1285); Frequency: Annually; 
Affected Public: Private Sector, Business or other for-profit and not-
for-profit institutions; Number of Respondents: 235; Number of 
Responses: 315; Total Annual Hours: 1,340. (For policy questions 
regarding this collection, contact Mohinee Mukherjee at 404-562-0151.)

William N. Parham, III
Director, Division of Information Collections and Regulatory Impacts, 
Office of Strategic Operations and Regulatory Affairs.
[FR Doc. 2026-10934 Filed 6-1-26; 8:45 am]
BILLING CODE 4120-01-P


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Indexed from Federal Register on June 2, 2026.

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