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.