Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB), 54160-54161 [E8-21669]

Download as PDF 54160 Federal Register / Vol. 73, No. 182 / Thursday, September 18, 2008 / Notices their obligations under the Communications Act, as amended. Federal Communications Commission. Marlene H. Dortch, Secretary. [FR Doc. E8–21864 Filed 9–17–08; 8:45 am] BILLING CODE 6712–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare and Medicaid Services [Document Identifier: CMS–10137 and CMS– 10237 and 10214] Emergency Clearance: Public Information Collection Requirements Submitted to the Office of Management and Budget (OMB) Center for Medicare and Medicaid Services, HHS. In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Centers for Medicare and Medicaid Services (CMS), Department of Health and Human Services, is publishing the following summary of proposed collections for public comment. Interested persons are invited to send comments regarding this burden estimate or any other aspect of this collection of information, including any of the following subjects: (1) The necessity and utility of the proposed information collection for the proper performance of the agency’s functions; (2) the accuracy of the estimated burden; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. We are, however, requesting an emergency review of the information collection referenced below. In compliance with the requirement of section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have submitted to the Office of Management and Budget (OMB) the following requirements for emergency review. We are requesting an emergency review because the collection of this information is needed before the expiration of the normal time limits under OMB’s regulations at 5 CFR part 1320(a)(2)(iii). This is necessary to ensure compliance with an initiative of the Administration. We cannot reasonably comply with the normal clearance procedures because the use of normal clearance procedures is dwashington3 on PRODPC61 with NOTICES AGENCY: VerDate Aug<31>2005 15:26 Sep 17, 2008 Jkt 214001 reasonably likely to cause a statutory deadline to be missed. The Balanced Budget Act of 1997, established a new ‘‘Part C’’ in the Medicare statute, sections 1851 through 1859 of the Social Security Act, which provided for a Medicare+Choice (M+C) program. The Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) was enacted on December 8, 2003. The MMA established the Medicare Prescription Drug Benefit Program under section 101 of the MMA and is codified in section 1860D of the Social Security Act which establishes the voluntary Prescription Drug Benefit Program (‘‘Part D’’), and made revisions to the provisions of Medicare Part C, governing what is now called the Medicare Advantage (MA) program (formerly Medicare+Choice). The MMA was amended on July 15, 2008 by the enactment of the Medicare Improvements for Patients and Providers Act of 2008 (MIPPA). CMS is in the process of publishing regulations that are intended to be released as an interim final rule with comment. Many of the provisions included in MIPPA that impact the Part C and Part D programs are selfimplementing, meaning these provisions will go into effect without any further regulatory clarification or changes to the Part C and Part D solicitations. As part of the revised information collection request, CMS will implement into the Part C solicitations, sections 163, 164, and 165 of MIPPA, and implement into the Part D solicitations, sections 171, 172 and 173 of MIPPA. These sections amend the contractual requirements that Part C and Part D sponsors (applicants) must have with CMS and with any downstream or related entities performing Part C and Part D functions on the sponsor’s behalf. Currently CMS provides templates that contain the required language for the contracts based on the statute and regulations. While applicants do not have to use the exact CMS contract templates, they will be responsible for including the required language in the contracts when they submit materials to CMS for the 2010 contract year. The solicitations do not represent new policy, but rather implement the provisions that will exist in the forthcoming regulations, and include clarifying edits and updates as well. Therefore, CMS is seeking an emergency PRA clearance to amend the Part C and Part D solicitations to reflect the new MIPPA requirements. 1. Type of Information Collection Request: Revision of a currently approved collection; Title of PO 00000 Frm 00027 Fmt 4703 Sfmt 4703 Information Collection: Application for Prescription Drug Plans (PDP); Application for Medicare Advantage Prescription Drug (MA–PD); Application for Cost Plans to Offer Qualified Prescription Drug Coverage; Application for Employer Group Waiver Plans to Offer Prescription Drug Coverage; Service Area Expansion Application for Prescription Drug Coverage; Use: Collection of this information is mandated in Part D of the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 and under supporting regulations Subpart K of 42 CFR 423 entitled ‘‘Application Procedures and Contracts with PDP Sponsors.’’ Coverage for the prescription drug benefit is provided through contracted prescription drug plans (PDPs) or through Medicare Advantage (MA) plans that offer integrated prescription drug and health care coverage (MA–PD plans). Cost Plans that are regulated under Section 1876 of the Social Security Act, and Employer Group Waiver Plans (EGWP) may also provide a Part D benefit. Organizations wishing to provide services under the Prescription Drug Benefit Program must complete an application, negotiate rates and receive final approval from CMS. Existing Part D Sponsors may also expand their contracted service area by completing the Service Area Expansion (SAE) application. The information will be collected under the solicitation of proposals from PDP, MA–PD, Cost Plan, PACE, and EGWP Plan applicants. The collected information will be used by CMS to: (1) Ensure that applicants meet CMS requirements, (2) support the determination of contract awards. Form Number: CMS–10137 (OMB#: 0938– 0936); Frequency: Reporting—Once; Affected Public: Business or other forprofit and Not-for-profit institutions; Number of Respondents: 455 Total Annual Responses: 455; Total Annual Hours: 11,890. 2. Type of Information Collection Request: Revision of a currently approved collection; Title of Information Collection: Medicare Advantage Applications—Part C; Use: Collection of this information is mandated in Part C of the Medicare Prescription Drug, Improvement and Modernization Act of 2003 (MMA) in Subpart K of 42 CRF 422 entitled ‘‘Contracts with Medicare Advantage Organizations.’’ Under section 1851(a)(1) of the Act, every individual entitled to Medicare Part A and enrolled under Part B, except for most individuals with end-stage renal disease, could elect to receive benefits either through the Original Medicare E:\FR\FM\18SEN1.SGM 18SEN1 54161 Federal Register / Vol. 73, No. 182 / Thursday, September 18, 2008 / Notices Program or an M+C plan, if one was offered where he or she lived. Coverage for the prescription drug benefit is provided through contracted prescription drug plans or through Medicare Advantage (MA) plans that offer integrated prescription drug and health care coverage (MA–PD plans). Cost plans that are required under section 1876 of the Social Security Act, and Employer Group Waiver Plans (EGWP) may also provide a Part D benefit. Organizations wishing to provide services under the MA and MA–PD plans must complete an application, negotiate rates and receive final approval from CMS. Certain existing MA plans may also expand their contracted area by completing the Service Area Expansion (SAE) application. The information will be collected under the solicitation of proposals from MA–PD, Cost Plan, EGWP Plan applicants. The collection information will be used by CMS to: (1) ensure that applicants meet CMS requirements, (2) support the determination of contract awards. Form Number: CMS–10237 and 10214 (OMB#: 0938–0935); Frequency: Reporting—Yearly; Affected Public: Business or other for-profit and Not-forprofit institutions; Number of Respondents: 267; Total Annual Responses: 267; Total Annual Hours: 6,709. CMS is requesting OMB review and approval of this collection by December 12, 2008, with a 180-day approval period. Written comments and recommendation will be considered from the public if received by the individuals designated below by the noted deadline below. To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’s Web site address at http://www.cms.hhs.gov/ PaperworkReductionActof1995 or Email your request, including your address, phone number, OMB number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call the Reports Clearance Office on (410) 786– 1326. In commenting on the proposed information collections please reference the document identifier or OMB control number. To be assured consideration, comments and recommendations must be submitted in one of the following ways by October 20, 2008: 1. Electronically. You may submit your comments electronically to http:// www.regulations.gov. Follow the instructions for ‘‘Comment or Submission’’ or ‘‘More Search Options’’ to find the information collection document(s) accepting comments. 2. By regular mail. You may mail written comments to the following address: CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development, Attention: Document Identifier/OMB Control Number llll, Room C4–26– 05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850; and, OMB Office of Information and Regulatory Affairs, Attention: CMS Desk Officer, New Executive Office Building, Room 10235, Washington, DC 20503, Fax Number: (202) 395–6974. Dated: September 8, 2008. Michelle Shortt, Director, Regulations Development Group, Office of Strategic Operations and Regulatory Affairs. [FR Doc. E8–21669 Filed 9–15–08; 9:00 am] BILLING CODE 4120–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Proposed Projects: Title: Interstate Referral Guide (IRG). OMB No.: 0970–0209. Description: The purpose of the Intergovernmental Referral Guide (IRG) project is to provide States, Foreign Nations and Tribes with an effective and efficient way of viewing and updating their profiles with child support enforcement policies and procedures, and their address and location code information by consolidating data available through numerous discrete sources into a centralized, automated repository. Respondents: State IV–D Child Support Programs, Foreign Nation Child Support Programs and Tribes. ANNUAL BURDEN ESTIMATES Number of respondents Number of responses per respondent IRG State User Guide (States and Territories) ............................................................... IRG State User Guide (Foreign Nations ......................................................................... IRG Tribal User Guide ..................................................................................................... 54 23 44 18 2 18 0.30 0.10 0.30 291.60 4.60 237.60 Estimated Total Annual Burden Hours ..................................................................... .................... .................... .................... 533.80 dwashington3 on PRODPC61 with NOTICES Instrument In compliance with the requirements of Section 506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to the Administration for Children and Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, VerDate Aug<31>2005 15:26 Sep 17, 2008 Jkt 214001 DC 20447, Attn: ACF Reports Clearance Officer. E-mail address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on: (a) Whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) PO 00000 Frm 00028 Fmt 4703 Sfmt 4703 Average burden hours per response Total burden hours the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. E:\FR\FM\18SEN1.SGM 18SEN1

Agencies

[Federal Register Volume 73, Number 182 (Thursday, September 18, 2008)]
[Notices]
[Pages 54160-54161]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-21669]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare and Medicaid Services

[Document Identifier: CMS-10137 and CMS-10237 and 10214]


Emergency Clearance: Public Information Collection Requirements 
Submitted to the Office of Management and Budget (OMB)

AGENCY: Center for Medicare and Medicaid Services, HHS.

    In compliance with the requirement of section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, the Centers for Medicare and Medicaid 
Services (CMS), Department of Health and Human Services, is publishing 
the following summary of proposed collections for public comment. 
Interested persons are invited to send comments regarding this burden 
estimate or any other aspect of this collection of information, 
including any of the following subjects: (1) The necessity and utility 
of the proposed information collection for the proper performance of 
the agency's functions; (2) the accuracy of the estimated burden; (3) 
ways to enhance the quality, utility, and clarity of the information to 
be collected; and (4) the use of automated collection techniques or 
other forms of information technology to minimize the information 
collection burden.
    We are, however, requesting an emergency review of the information 
collection referenced below. In compliance with the requirement of 
section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, we have 
submitted to the Office of Management and Budget (OMB) the following 
requirements for emergency review. We are requesting an emergency 
review because the collection of this information is needed before the 
expiration of the normal time limits under OMB's regulations at 5 CFR 
part 1320(a)(2)(iii). This is necessary to ensure compliance with an 
initiative of the Administration. We cannot reasonably comply with the 
normal clearance procedures because the use of normal clearance 
procedures is reasonably likely to cause a statutory deadline to be 
missed.
    The Balanced Budget Act of 1997, established a new ``Part C'' in 
the Medicare statute, sections 1851 through 1859 of the Social Security 
Act, which provided for a Medicare+Choice (M+C) program. The Medicare 
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) was 
enacted on December 8, 2003. The MMA established the Medicare 
Prescription Drug Benefit Program under section 101 of the MMA and is 
codified in section 1860D of the Social Security Act which establishes 
the voluntary Prescription Drug Benefit Program (``Part D''), and made 
revisions to the provisions of Medicare Part C, governing what is now 
called the Medicare Advantage (MA) program (formerly Medicare+Choice). 
The MMA was amended on July 15, 2008 by the enactment of the Medicare 
Improvements for Patients and Providers Act of 2008 (MIPPA).
    CMS is in the process of publishing regulations that are intended 
to be released as an interim final rule with comment. Many of the 
provisions included in MIPPA that impact the Part C and Part D programs 
are self-implementing, meaning these provisions will go into effect 
without any further regulatory clarification or changes to the Part C 
and Part D solicitations. As part of the revised information collection 
request, CMS will implement into the Part C solicitations, sections 
163, 164, and 165 of MIPPA, and implement into the Part D 
solicitations, sections 171, 172 and 173 of MIPPA. These sections amend 
the contractual requirements that Part C and Part D sponsors 
(applicants) must have with CMS and with any downstream or related 
entities performing Part C and Part D functions on the sponsor's 
behalf. Currently CMS provides templates that contain the required 
language for the contracts based on the statute and regulations. While 
applicants do not have to use the exact CMS contract templates, they 
will be responsible for including the required language in the 
contracts when they submit materials to CMS for the 2010 contract year.
    The solicitations do not represent new policy, but rather implement 
the provisions that will exist in the forthcoming regulations, and 
include clarifying edits and updates as well. Therefore, CMS is seeking 
an emergency PRA clearance to amend the Part C and Part D solicitations 
to reflect the new MIPPA requirements.
    1. Type of Information Collection Request: Revision of a currently 
approved collection; Title of Information Collection: Application for 
Prescription Drug Plans (PDP); Application for Medicare Advantage 
Prescription Drug (MA-PD); Application for Cost Plans to Offer 
Qualified Prescription Drug Coverage; Application for Employer Group 
Waiver Plans to Offer Prescription Drug Coverage; Service Area 
Expansion Application for Prescription Drug Coverage; Use: Collection 
of this information is mandated in Part D of the Medicare Prescription 
Drug, Improvement, and Modernization Act of 2003 and under supporting 
regulations Subpart K of 42 CFR 423 entitled ``Application Procedures 
and Contracts with PDP Sponsors.''
    Coverage for the prescription drug benefit is provided through 
contracted prescription drug plans (PDPs) or through Medicare Advantage 
(MA) plans that offer integrated prescription drug and health care 
coverage (MA-PD plans). Cost Plans that are regulated under Section 
1876 of the Social Security Act, and Employer Group Waiver Plans (EGWP) 
may also provide a Part D benefit. Organizations wishing to provide 
services under the Prescription Drug Benefit Program must complete an 
application, negotiate rates and receive final approval from CMS. 
Existing Part D Sponsors may also expand their contracted service area 
by completing the Service Area Expansion (SAE) application. The 
information will be collected under the solicitation of proposals from 
PDP, MA-PD, Cost Plan, PACE, and EGWP Plan applicants. The collected 
information will be used by CMS to: (1) Ensure that applicants meet CMS 
requirements, (2) support the determination of contract awards. Form 
Number: CMS-10137 (OMB: 0938-0936); Frequency: Reporting--
Once; Affected Public: Business or other for-profit and Not-for-profit 
institutions; Number of Respondents: 455 Total Annual Responses: 455; 
Total Annual Hours: 11,890.
    2. Type of Information Collection Request: Revision of a currently 
approved collection; Title of Information Collection: Medicare 
Advantage Applications--Part C; Use: Collection of this information is 
mandated in Part C of the Medicare Prescription Drug, Improvement and 
Modernization Act of 2003 (MMA) in Subpart K of 42 CRF 422 entitled 
``Contracts with Medicare Advantage Organizations.'' Under section 
1851(a)(1) of the Act, every individual entitled to Medicare Part A and 
enrolled under Part B, except for most individuals with end-stage renal 
disease, could elect to receive benefits either through the Original 
Medicare

[[Page 54161]]

Program or an M+C plan, if one was offered where he or she lived.
    Coverage for the prescription drug benefit is provided through 
contracted prescription drug plans or through Medicare Advantage (MA) 
plans that offer integrated prescription drug and health care coverage 
(MA-PD plans). Cost plans that are required under section 1876 of the 
Social Security Act, and Employer Group Waiver Plans (EGWP) may also 
provide a Part D benefit. Organizations wishing to provide services 
under the MA and MA-PD plans must complete an application, negotiate 
rates and receive final approval from CMS. Certain existing MA plans 
may also expand their contracted area by completing the Service Area 
Expansion (SAE) application. The information will be collected under 
the solicitation of proposals from MA-PD, Cost Plan, EGWP Plan 
applicants. The collection information will be used by CMS to: (1) 
ensure that applicants meet CMS requirements, (2) support the 
determination of contract awards. Form Number: CMS-10237 and 10214 
(OMB: 0938-0935); Frequency: Reporting--Yearly; Affected 
Public: Business or other for-profit and Not-for-profit institutions; 
Number of Respondents: 267; Total Annual Responses: 267; Total Annual 
Hours: 6,709.
    CMS is requesting OMB review and approval of this collection by 
December 12, 2008, with a 180-day approval period. Written comments and 
recommendation will be considered from the public if received by the 
individuals designated below by the noted deadline below.
    To obtain copies of the supporting statement and any related forms 
for the proposed paperwork collections referenced above, access CMS's 
Web site address at http://www.cms.hhs.gov/PaperworkReductionActof1995 
or E-mail your request, including your address, phone number, OMB 
number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call 
the Reports Clearance Office on (410) 786-1326.
    In commenting on the proposed information collections please 
reference the document identifier or OMB control number. To be assured 
consideration, comments and recommendations must be submitted in one of 
the following ways by October 20, 2008:
    1. Electronically. You may submit your comments electronically to 
http://www.regulations.gov. Follow the instructions for ``Comment or 
Submission'' or ``More Search Options'' to find the information 
collection document(s) accepting comments.
    2. By regular mail. You may mail written comments to the following 
address: CMS, Office of Strategic Operations and Regulatory Affairs, 
Division of Regulations Development, Attention: Document Identifier/OMB 
Control Number --------, Room C4-26-05, 7500 Security Boulevard, 
Baltimore, Maryland 21244-1850; and, OMB Office of Information and 
Regulatory Affairs, Attention: CMS Desk Officer, New Executive Office 
Building, Room 10235, Washington, DC 20503, Fax Number: (202) 395-6974.

    Dated: September 8, 2008.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations 
and Regulatory Affairs.
[FR Doc. E8-21669 Filed 9-15-08; 9:00 am]
BILLING CODE 4120-01-P