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

Forms and Documents

Document Name	Status
Form CMS-10527 Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP) Form and Instruction	Unchanged
Form CMS-10527 Product Discontinuance Notice for QHP Issuers Form and Instruction	Unchanged
Form CMS-10527 Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP) Form and Instruction	Unchanged
Form CMS-10527 Product Renewal and Discontinuance Notice for QHP Issuers Form and Instruction	Unchanged
CMS-10527 Change Request Attachment - Updated Renewal and Discontinuation Notices Individual Market Redline.docx Supplementary Document	2019-04-12
CMS-10527 - Change Request Attachment - Updated Renewal and Discontinuation Notices Individual Market Clean.docx Supplementary Document	2019-04-12
CMS-10527 - Change Request Crosswalk.docx Supplementary Document	2019-04-12
CMS-10527 Supporting Statement.docx Supporting Statement A	2019-04-12
CMS-10527 - Non-substantive Change Request Justifiation.docx Justification for No Material/Nonsubstantive Change	2019-04-12
CMS-10527 Updated Federal Standard Renewal and Product Discontinuation Notices -Clean.docx Supplementary Document	2018-08-02
CMS-10527 Updated Federal Standard Renewal and Product Discontinuation Notices COMPARE.pdf Supplementary Document	2018-08-23
CMS-10527 - NonSubstantive Change request.docx Justification for No Material/Nonsubstantive Change	2018-08-02
CMS- 10527 Appendix A - Comment and Response Document.pdf Supplementary Document	2016-09-19

IC Document Collections

IC ID	Document Title	Status
212940	Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP) Form and Instruction	Unchanged
212939	Product Discontinuance Notice for QHP Issuers Form and Instruction	Unchanged
212938	Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP) Form and Instruction	Unchanged
212937	Product Renewal and Discontinuance Notice for QHP Issuers Form and Instruction	Unchanged

ICR Details

OMB Control No: 0938-1254	ICR Reference No: 201904-0938-008
Status: Historical Active	Previous ICR Reference No: 201808-0938-001
Agency/Subagency: HHS/CMS	Agency Tracking No: CCIIO
Title: Annual Eligibility Redetermination, Product Discontinuation and Renewal Notices (CMS-10527)
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 06/20/2019
	Date Received in OIRA: 04/12/2019
Terms of Clearance: We would appreciate it if CMS could please update the instrument in ROCIS.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	10/31/2019	10/31/2019	10/31/2019
Responses	11,594	0	11,594
Time Burden (Hours)	149,188	0	149,188
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:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	81 FR 25406	04/21/2016
30-day Notice:	Federal Register Citation:	Citation Date:
	81 FR 63762	09/16/2016
Did the Agency receive public comments on this ICR? Yes

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

IC Title	Form No.	Form Name
Product Discontinuance Notice for QHP Issuers	CMS-10527	Discontinuation Notices
Product Renewal and Discontinuance Notice for QHP Issuers	CMS-10527	Discontinuance and Renewal Notice
Product Discontinuance Notice for Issuers Outside the Marketplace (Non-QHP)	CMS-10527	Discontinuation Notices
Product Renewal Notice for Issuers Outside the Marketplace (Non-QHP)	CMS-10527	Renewal Notice

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ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	11,594	11,594	0	0	0	0
Annual Time Burden (Hours)	149,188	149,188	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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:

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Annual Cost to Federal Government: $0

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? Uncollected

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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: 04/12/2019

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