Annual Eligibility Redetermination, Product Discontinuation and Renewal Notices (CMS-10527)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form CMS-10527 Federal Standard Notices	Form and Instruction	Modified	Available
Form CMS-10527 Discontinuation Notices	Form and Instruction	Modified	Available
Form CMS-10527 Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified	Repair queued
Form CMS-10527 Discontinuation without auto enrollment (QHP)	Form and Instruction	Modified	Available
Form CMS-10527 Discontinuation Notices	Form and Instruction	Modified	Available
Form CMS-10527 Product Discontinuance Notice for QHP Issuers	Form and Instruction	Modified	Repair queued
Form CMS-10527 Renewal Notice	Form and Instruction	Modified	Available
Form CMS-10527 Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified	Repair queued
Form CMS-10527 Renewal and Discontinuance Notice	Form and Instruction	Modified	Available
Form CMS-10527 Product Renewal and Discontinuance Notice for QHP Issuers	Form and Instruction	Modified	Available
CMS-10527 Summary of Changes (Attachments - Notices)_60-day.docx	Supplementary Document	Uploaded 2025-04-17	Available
CMS-10527 Summary of Changes (Attachments - Notices)_60-day.docx	Supplementary Document	Uploaded 2025-04-17	Repair queued
CMS-10527 - Supporting Statement NPRM.docx	Supporting Statement A	Uploaded 2025-04-10	Repair queued
CMS-10527 - Supporting Statement NPRM.docx	Supporting Statement A	Uploaded 2025-04-10	Repair queued
CMS-10527 Summary of Changes.pdf	Supplementary Document	Uploaded 2023-04-26	Repair queued
CMS-10527 Summary of Changes.pdf	Supplementary Document	Uploaded 2023-04-26	Repair queued
CMS-10527 Comment and Response Summary 30d comment period rev.docx	Supplementary Document	Uploaded 2023-06-08	Repair queued
CMS-10527 Comment and Response Summary 30d comment period rev.docx	Supplementary Document	Uploaded 2023-06-08	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
212940	Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified	Federal Standard Notices
212940	Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified	Discontinuation Notices
212940	Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified
212939	Product Discontinuance Notice for QHP Issuers	Form and Instruction	Modified	Discontinuation without auto enrollment (QHP)
212939	Product Discontinuance Notice for QHP Issuers	Form and Instruction	Modified	Discontinuation Notices
212939	Product Discontinuance Notice for QHP Issuers	Form and Instruction	Modified
212938	Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified	Renewal Notice
212938	Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP)	Form and Instruction	Modified
212937	Product Renewal and Discontinuance Notice for QHP Issuers	Form and Instruction	Modified	Renewal and Discontinuance Notice
212937	Product Renewal and Discontinuance Notice for QHP Issuers	Form and Instruction	Modified

ICR Details

OMB Control No: 0938-1254	ICR Reference No: 202504-0938-012
Status: Historical Inactive	Previous ICR Reference No: 202304-0938-018
Agency/Subagency: HHS/CMS	Agency Tracking No: CCIIO
Title: Annual Eligibility Redetermination, Product Discontinuation and Renewal Notices (CMS-10527)
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Comment filed on proposed rule and continue	Conclusion Date: 06/26/2025
Retrieve Notice of Action (NOA)	Date Received in OIRA: 04/18/2025
Terms of Clearance: In accordance with 5 CFR 1320, the information collection is not approved at this time. Prior to publication of the final rule, the agency should provide to OIRA a summary of all comments received on the proposed information collection and identify any changes made in response to these comments.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	06/30/2026	36 Months From Approved	06/30/2026
Responses	5,881	0	5,881
Time Burden (Hours)	72,002	0	72,002
Cost Burden (Dollars)	0	0	0

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Abstract: The final rule "Patient Protection and Affordable Care Act; Annual Eligibility Redeterminations for Exchange Participation and Insurance Affordability Programs; Health Insurance Issuer Standards Under the Affordable Care Act, Including Standards Related to Exchanges", provides that a Marketplace may choose to conduct the annual redetermination process for a plan year (1) in accordance with the existing procedures described in 45 CFR 155.335; (2) in accordance with procedures described in guidance issued by the Secretary for the coverage year; or (3) using an alternative proposed by the Marketplace and approved by the Secretary. The guidance document "Guidance on Annual Redeterminations for Coverage for 2015" contains the procedures that the Secretary is specifying for the 2015 coverage year, as noted in (2) above. These procedures will be adopted by the Federally-facilitated Marketplace. Under this option, the Marketplace will provide three notices. The final rule also amends the requirements for product renewal and re-enrollment (or nonrenewal) notices to be sent by Qualified Health Plan (QHP) issuers in the Exchanges and specifies content for these notices. The accompanying guidance document "Form and Manner of Notices When Discontinuing or Renewing a Product in the Group or Individual Market" provides standard notices for product discontinuation and renewal to be sent by issuers of QHPs and issuers in the individual market. Issuers in the small group market may use the draft Federal standard small group notices released in the June 26, 2014 bulletin "Draft Standard Notices When Discontinuing or Renewing a Product in the Small Group or Individual Market", or any forms of the notice otherwise permitted by applicable laws and regulations. States that are enforcing the Affordable Care Act may develop their own standard notices, for product discontinuances, renewals, or both, provided the State-developed notices are at least as protective as the Federal standard notices.

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Authorizing Statute(s): PL: Pub.L. 111 - 148 1411(f)(1)(B) Name of Law: Affordable Care Act
  

Citations for New Statutory Requirements: PL: Pub.L. 111 - 148 Section 1411(f)(1)(B) Name of Law: Affordable Care Act

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
0938-AV61	Proposed rulemaking	90 FR 12942	03/19/2025

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 4

table that charts list of burden

IC Title	Form No.	Form Name
Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP)	CMS-10527	Renewal Notice
Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	CMS-10527, CMS-10527	Discontinuation Notices ,   Federal Standard Notices
Product Discontinuance Notice for QHP Issuers	CMS-10527, CMS-10527	Discontinuation Notices ,   Discontinuation without auto enrollment (QHP)
Product Renewal and Discontinuance Notice for QHP Issuers	CMS-10527	Renewal and Discontinuance Notice

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Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: The burden for individual market QHP issuers has increased by approximately 423 hours (from 12,821 to 13,244) due to an increase in the estimated number of QHP issuers (from 333 to 344). The burden for issuers in the individual market outside the Exchange and issuers in the small group market has decreased by 6,335 hours (from 59,326 to 52,992) due to a decrease in the estimated number of issuers in those markets (from 1,340 to 1,206). In total, there is a reduction in burden by approximately 5,786 hours. (from 72,002 to 66,236 hours),

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Annual Cost to Federal Government: $5,012

Does this IC contain surveys, censuses, or employ statistical methods? No

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Yes

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? No

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 04/18/2025

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