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.
When we last cleared this IC in
2017, the burden was 37 hours. However, we are currently reporting
a burden of 28 hours. This change stems a decrease in the number of
responses from 425 to 335. There is no change to the burden time
per response. Although the number of responses changed, SSA did not
take any actions to cause this change. These figures represent
current Management Information data.
$66,559
No
Yes
Yes
No
No
No
No
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.