Document
Agency Information Collection Activities: Submission for OMB Review; Comment Request
The Centers for Medicare & Medicaid Services (CMS) is announcing an opportunity for the public to comment on CMS' intention to collect information from the public. Under the Pap...
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501-3520), federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. The term “collection of information” is defined in 44 U.S.C. 3502(3) and 5 CFR 1320.3(c) and includes agency requests or requirements that members of the public submit reports, keep records, or provide information to a third party. Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires federal agencies to publish a 30-day notice in the
Federal Register
concerning each proposed collection of information, including each proposed extension or reinstatement of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, CMS is publishing this notice that summarizes the following proposed collection(s) of information for public comment:
1.
Type of Information Collection Request:
New collection;
Title of Information Collection:
Model Medicare Advantage and Medicare Prescription Drug Plan Individual Enrollment Request Form;
Use:
This information collection is necessary for the Medicare beneficiary (or their legal representative), to enroll in an MA or PDP plan, even if switching plans within the same MA or PDP organization. To consider an election complete, the individual must:
- Complete an enrollment request;
- Provide required information to the MA or PDP organization within the required time frames;
- Submit the completed request to the MA or PDP organization during a valid enrollment period.
- MA and PDP organizations, applicants to MA and PDP organizations, and the CMS will use the information collected to comply with the eligibility and enrollment requirements for Medicare Part C and Part D plans.
Section 4001 of the Balanced Budget Act of 1997 (BBA) (Pub. L. 105-33) enacted August 5, 1997, established Part C of the Medicare program, known as the Medicare + Choice program, (now referred to as Medicare Advantage (MA)). As required by 42 CFR 422.50(a)(5), an MA-eligible individual who meets the eligibility requirements for enrollment into an MA or MAPD plan may enroll during the enrollment periods specified in § 422.62, by completing an enrollment form with the MA organization or enrolling through other mechanisms that CMS determines are appropriate.
Section 101 of Title I of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) (Pub. L. 108-173) enacted December 8, 2003, established Part D of the Medicare program, known as the Voluntary Prescription Drug Benefit Program. As required by 42 CFR 423.32(a) and (b), a Part D-eligible individual who wishes to enroll in a Medicare prescription drug plan (PDP) may enroll during the enrollment periods specified in § 423.38, by completing an enrollment form with the PDP, or enrolling through other mechanisms CMS determines are appropriate.
Form Number:
CMS-10718 (OMB control number: 0938-New);
Frequency:
Yearly;
Affected Public:
State, Local, or Tribal Governments;
Number of Respondents:
14,749,256;
Total Annual Responses:
14,749,256;
Total Annual Hours:
7,861,354. (For policy questions regarding this collection contact Deme Umo at (410) 786-8854.)
2.
Type of Information Collection Request:
Revision of a currently approved collection;
Title of Information Collection:
Reconciliation of State Invoice (ROSI) and Prior Quarter Adjustment Statement (PQAS);
Use:
Form CMS-304 (ROSI) is used by manufacturers to respond to the state's rebate invoice for current quarter utilization. Form CMS-304a (PQAS) is required only in those instances where a change to the original rebate data submittal is necessary.
Form Number:
CMS-304 and -304a (OMB control number: 0938-0676);
Frequency:
Quarterly;
Affected Public:
Business or other for-profits;
Number of Respondents:
1,255;
Total Annual Responses:
5,020;
Total Annual Hours:
227,416. (For policy questions regarding this collection contact Andrea Wellington at 410-786-3490.)
3.
Type of Information Collection Request:
Revision of a currently approved collection;
Title of Information Collection:
Medicaid Drug Rebate State Reporting Program Forms;
Use:
We develop the rebate amount per drug unit from information supplied by the drug manufacturers and distributes these data to the states. States then must report quarterly to the drug manufacturers and report to us the total number of units of each dosage form/strength of their covered outpatient drugs reimbursed during a quarter and the rebate amount to be refunded. This report is due within 60 days of the end of each calendar quarter. The information in the report is based on claims paid by the state Medicaid agency during a calendar quarter. Form CMS-R-144 (Quarterly Report Data) is required from states quarterly to report utilization for any drugs paid for during that quarter. Form CMS-368 (Administrative Data) is required only in those instances where a change to the original data submittal is necessary.
Form Number:
CMS-368 and -R-144 (OMB control number: 0938-0582);
Frequency:
Quarterly and on occasion;
Affected Public:
State, Local, or Tribal Governments;
Number of Respondents:
56;
Total Annual Responses:
234;
Total Annual Hours:
12,101. (For policy questions regarding this collection contact Shannon Evans at 410-786-3083.)
Dated: March 3, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and Regulatory Affairs.