In accordance
with 5 CFR 1320, the information collection is approved for three
years.
Inventory as of this Action
Requested
Previously Approved
12/31/2020
36 Months From Approved
12/31/2017
426
0
461
37
0
41
0
0
0
The Medicare Prescription Drug
Improvement, and Modernization Act of 2003 (MMA) established the
Medicare Part D program for voluntary prescription drug coverage of
premium, deductible, and co-payment costs for certain low-income
individuals. The MMA also mandated the provision of subsidies for
those individuals who qualify for the program and who meet
eligibility criteria for help with premium, deductible, or
co-payment costs. This law requires SSA to make eligibility
determinations and to provide a process for appealing SSA's
determinations. Regulation sections 418.3625(c), 418.3645,
418.3665(a), and 418.3670 contain public reporting requirements
pertaining to administrative review hearings. Respondents are
applicants for the Medicare Part D subsidies who request an
administrative review hearing.
The decrease in burden stems
from a decrease in the number of respondents requesting
administrative review.
$0
No
Yes
Yes
No
No
No
Uncollected
Faye Lipsky 410 965-8783
faye.lipsky@ssa.gov
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.