The Medicare Modernization Act of 2003
mandated the creation of the Medicare Part D prescription drug
coverage program and provided for certain subsidies for eligible
Medicare beneficiaries to help pay for the costs of prescription
drugs. SSA uses Form SSA-1020 (and the i1020, its electronic
counterpart), the Application for Extra Help with Medicare
Prescription Drug Plan Costs, to collect information to make Part D
subsidy eligibility determinations. In this non-substantive change
request, we are making minor wording and organizational changes to
the Welcome/Introductory screens of the i1020. There is no
difference in the type of information we are asking, and these
changes will not affect burden.
PL:
Pub.L. 110 - 275 100 Name of Law: Medicare Improvements for
Patients and Providers Act of 2008
US Code:
42 USC 1395w-101 Name of Law: Social Security Act
PL: Pub.L. 110 - 275 100 Name of Law:
Medicare Improvements for Patients and Providers Act of
2008
There has been an increase in
burden hours. The increase stems from and increase in the number of
respondents competing the application. There has been a decrease in
burden hours, because we are no longer sending the MSP follow-up
letter.
$3,812,150
No
No
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.