In accordance with 5 CFR 1320, the information collection is approved for 6 months. In their next submission, the agency must identify the specific regulatory provisions, citing the appropriate section or provision of the CFR for each IC, for which they are requesting PRA approval and provide any instructions or guidance to the respondents. The agency is also reminded to provide burden estimates based on the annual average of burden imposed over 3 years. Finally, the prior terms of clearance remain in effect: By the time of the next submission, the agency will provide an overview of the steps taken to minimize burden and avoid duplicative collections, especially with regard to the preliminary and secondary justifications.
Inventory as of this Action
Requested
Previously Approved
04/30/2012
6 Months From Approved
08/31/2014
3,901
0
3,435
91,219
0
86,656
0
0
0
This information collection request covers the Rate Increase Disclosure and Review Reporting Requirements of 45 CFR Part 154.
The number of respondents has increased to include association plans and the burden has been adjusted accordingly. We also corrected an arithmetic error regarding the one-Time health insurance issuer start-up costs.
$3,886,920
No
No
Yes
No
No
Uncollected
William Parham 4107864669
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:
(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;
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.