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Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View ICR - OIRA Conclusion
OMB Control No:
0938-0702
ICR Reference No:
202210-0938-005
Status:
Active
Previous ICR Reference No:
201905-0938-005
Agency/Subagency:
HHS/CMS
Agency Tracking No:
CCIIO-10430
Title:
Compliance with Individual and Group Market Reforms under Title XXVII of the Public Health Service Act (CMS-10430)
Type of Information Collection:
Extension without change of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
11/18/2022
Retrieve Notice of Action (NOA)
Date Received in OIRA:
10/17/2022
Terms of Clearance:
Inventory as of this Action
Requested
Previously Approved
Expiration Date
11/30/2025
36 Months From Approved
12/31/2022
Responses
51,385
0
42,120
Time Burden (Hours)
1,786
0
1,721
Cost Burden (Dollars)
0
0
0
Abstract:
Sections 2723 and 2761 of the Public Health Service Act (PHS Act) direct the Centers for Medicare and Medicaid Services (CMS) to enforce a provision (or provisions) of title XXVII of the PHS Act (including the implementing regulations in parts 144, 146, 147, and 148 of title 45 of the Code of Federal Regulations) with respect to health insurance issuers when a state has notified CMS that it has not enacted legislation to enforce or that it is not otherwise enforcing a provision (or provisions) of the group and individual market reforms with respect to health insurance issuers, or when CMS has determined that a state is not substantially enforcing one or more of those provisions. This collection of information includes requirements that are necessary for CMS to conduct compliance review activities.
Authorizing Statute(s):
PL:
Pub.L. 111 - 148 Title I
Name of Law: Affordable Care Act
US Code:
42 USC 300gg-23
Name of Law: Individual and Group Market Reforms
US Code:
42 USC 241
Name of Law: Research and investigations generally
PL:
Pub.L. 105 - 277 Title IX
Name of Law: The Women's Health and Cancer Rights Act of 1998
PL:
Pub.L. 104 - 204 Title VI
Name of Law: Newborns' and Mothers' Health Protection Act of 1996
PL:
Pub.L. 104 - 191 Title I
Name of Law: Health Insurance Portability and Accountability Act of 1996 (HIPAA)
PL:
Pub.L. 110 - 343 Title V
Name of Law: Paul Wellstone and Pete Domenici Mental Health Parity and Addiction Equity Act of 2008
PL:
Pub.L. 110 - 223 Title I
Name of Law: Genetic Information Nondiscrimination Act of 2008
US Code:
42 USC 300gg-61
Name of Law: Individual Market Rules
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
87 FR 32028
05/26/2022
30-day Notice:
Federal Register Citation:
Citation Date:
87 FR 51985
08/24/2022
Did the Agency receive public comments on this ICR?
No
Number of Information Collection (IC) in this ICR:
1
IC Title
Form No.
Form Name
Information Collection Requirements for Compliance with Individual and Group Market Reforms under Title XXVII of the Public Health Service Act
CMS-10430
Model Notice to Enrollees
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
51,385
42,120
0
0
9,265
0
Annual Time Burden (Hours)
1,786
1,721
0
0
65
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:
The estimated burden related to form filing submissions has decreased by 35 hours (from 364 to 329) due to the reduction in the estimated number of issuers (from 52 to 47) that submit forms for CMS’ review. The estimated burden related to full disclosure by issuers to all small employers of materials on all products and other information has decreased by 92 hours (from 774 to 682) due to a reduction in the estimated number of issuers affected by this requirement (from 387 to 341). The estimated burden related to opt-out notices has increased by 30 hours (from 145 hours to 175 hours) due to an increase in the estimated number of plans opting out (from 290 to 350). The burden related to state engagement coordination has increased by 162.5 hours (from 437.5 to 600) due to an increase in the burden per response (from 2.5 to 3) and an increase in the estimated number of responses (from 175 to 200). Therefore, total burden hours have increased by 65.5 hours (from 1720.5 to 1786).
Annual Cost to Federal Government:
$1,930,245
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
Agency Contact:
Jamaa Hill 301 492-4190
Common Form ICR:
No
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:
10/17/2022
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