Agency Information Collection Activities; Proposed Collection; Comment Request, 50372-50373 [E7-17351]

Download as PDF 50372 Federal Register / Vol. 72, No. 169 / Friday, August 31, 2007 / Notices Statement of Organization Functions, and Delegations of Authority of the Department of Health and Human Services (45 FR 67772–76, dated October 14, 1980, and corrected at 45 FR 69296, October 20, 1980, as amended most recently at 70 FR 72842–72843, dated December 7, 2005), the Division for Heart Disease and Stroke Prevention, National Center for Chronic Disease Prevention and Health Promotion, Centers for Disease Control and Prevention was established. This Division plans, directs, and coordinates programs to reduce morbidity, risk factors, costs, disability, mortality, and disparities associated with heart disease, stroke, and other cardiovascular disease outcomes. Under this Division, formative research was conducted to identify effective interventions and promising practices for preventing heart disease and stroke at the work site. In 2005, this research resulted in the development of a Successful Business Strategies to Prevent Heart Disease and Stroke Toolkit. The toolkit provides state programs with suggestions about which health benefits, services, and interventions can improve employee cardiovascular health, prevent heart disease and stroke, and reduce related costs. The second phase of this project focuses on disseminating and evaluating the Successful Business Strategies to Prevent Heart Disease and Stroke Toolkit. As part of the Toolkit evaluation, the CDC has employed contractor support to design and conduct a Web-based survey of State Health Departments to gather information on their experiences with the Toolkit. The contractor will collect and analyze all data from this survey. The CDC has also contracted to make revisions to the toolkit based on results of this survey, ongoing feedback from the States, and feedback from employers through interviews. There are no costs to respondents except their time to complete the survey. The total estimated annualized burden hours are 26. ESTIMATED ANNUALIZED BURDEN HOURS Form Web-based survey on CVH Toolkit. State Heart Disease and Stroke Programs. Dated: August 23, 2007. Maryam I. Daneshvar, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. E7–17293 Filed 8–30–07; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Medicare & Medicaid Services [Document Identifier: CMS–10249 and CMS– 10120] Agency Information Collection Activities; Proposed Collection; Comment Request Centers for Medicare & 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 & Medicaid Services (CMS) 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 sroberts on PROD1PC70 with NOTICES AGENCY: VerDate Aug<31>2005 00:43 Aug 31, 2007 No. of respondents Respondents Jkt 211001 No. of responses per respondent Average burden per response (in hours) Total burden (in hours) 51 1 30/60 26 be collected; and (4) the use of automated collection techniques or other forms of information technology to minimize the information collection burden. 1. Type of Information Collection Request: New Collection; Title of Information Collection: Administrative Requirements for section 6071 of the Deficit Reduction Act of 2005 (DRA); Use: CMS will use an Operational Protocol Instruction Guide and template for the development of Operational Protocols for the States selected to participate in the Money Follows the Person (MFP) Rebalancing Demonstration. The guide will provide instruction on the required elements of the State’s Operational Protocol, which must be submitted and approved before a State may enroll individuals in the State’s demonstration program or begin to claim service dollars. The DRA Section 6071(c)(9) requires the States to provide information and assurances that total expenditures under the State Medicaid program for home and community-based long-term care services will not be less for any fiscal year during the MFP demonstration project than for the greater of such expenditures for fiscal year 2005 or any succeeding fiscal year before the first of the year of the MFP demonstration project. Accordingly, States are required to submit Maintenance of Effort (MOE) forms and MFP Budget forms on an annual basis. Additionally, in order to receive enhanced FMAP, States are required to submit the MFP PO 00000 Frm 00051 Fmt 4703 Sfmt 4703 Demonstration Financial Forms on a quarterly basis. Section 6071(g) of the DRA requires a national evaluation of the MFP demonstration project and a final report to the President and Congress. For the national evaluation, States will be required to submit semiannual reports that describe their progress in implementing their MFP programs and rebalancing their longterm care systems. In addition, States will be required to submit on a quarterly basis an MFP Finders File, which will include eligibility records for all MFP participants, and an MFP Services File, which will include records for each service funded with MFP grant funds. Form Number: CMS–10249 (OMB#: 0938–NEW); Frequency: Reporting— Yearly, Quarterly, Semi-annually and Once; Affected Public: States, Local or Tribal Governments; Number of Respondents: 31; Total Annual Responses: 229.4; Total Annual Hours: 7,843. 2. Type of Information Collection Request: Extension without change of a currently approved collection; Title of Information Collection: 1932 State Plan Amendment Template, State Plan Requirements and Supporting Regulations in 42 CFR 438.50; Form No.: CMS–10120 (OMB# 0938–0933); Use: The State Medicaid Agencies will complete the template. CMS will review the information to determine if the State has met all the requirements under 1932(1)(1)(A) and 42 CFR 438.50. Once all requirements are met, the State will be allowed to enroll Medicaid E:\FR\FM\31AUN1.SGM 31AUN1 Federal Register / Vol. 72, No. 169 / Friday, August 31, 2007 / Notices beneficiaries on a mandatory basis into managed care entities without section 1115 or 1915(b) waiver authority; Frequency: On occasion; Affected Public: State, local, or tribal government; Number of Respondents: 56; Total Annual Responses: 10; Total Annual Hours: 100. To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web Site address at https://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. To be assured consideration, comments and recommendations for the proposed information collections must be received at the address below, no later than 5 p.m. on October 30, 2007. CMS, Office of Strategic Operations and Regulatory Affairs, Division of Regulations Development—A, Attention: Melissa Musotto, Room C4–26–05, 7500 Security Boulevard, Baltimore, Maryland 21244–1850. conducting of adolescent pregnancy approaches. They are the only research group currently conducting a study of size and scope that provides for access to schools and study participants for the collection of additional data needed. Building on the existing study already underway saves the cost of initiating a study from the ground up. FOR FURTHER INFORMATION CONTACT: Stan Koutstaal, Ph.D., Director, Division of Abstinence Education, Family and Youth Services Bureau, ACYF, ACF, DHHS. Portals Building, Suite 800, 1250 Maryland Avenue, SW., Washington, DC 20024; 202–401–6959. Dated: August 24, 2007. Michelle Shortt, Director, Regulations Development Group, Office of Strategic Operations and Regulatory Affairs. [FR Doc. E7–17351 Filed 8–30–07; 8:45 am] Agency Information Collection Activities; Proposed Collection; Comment Request; Medical Devices: Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use BILLING CODE 4120–01–P Administration on Children, Youth, and Families (ACYF), ACF, DHHS. ACTION: Notice. AGENCY: sroberts on PROD1PC70 with NOTICES Food and Drug Administration [Docket No. 2007N–0325] ACTION: Notice of Award of Non-Competitive Grant CFDA No.: 93.010, Community-Based Abstinence Education. Legislative Authority: Title XI, Section 1110 of the Social Security Act. Amount of Award: $2,500,000. Project Period: September 30, 2007– March 30, 2009 (18 months). Justification for the Exception to Competition: ACYF will award service grant funds without competition to the Prevention Research Center at the University of Texas Health Science Center at Houston to build on a longitudinal study they are currently Jkt 211001 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration, HHS. Administration for Children and Families 00:43 Aug 31, 2007 BILLING CODE 4184–01–P AGENCY: DEPARTMENT OF HEALTH AND HUMAN SERVICES VerDate Aug<31>2005 Dated: August 24, 2007. Joan E. Ohl, Commissioner, Administration on Children, Youth and Families. [FR Doc. E7–17216 Filed 8–30–07; 8:45 am] Notice SUMMARY: The Food and Drug Administration (FDA) is announcing an opportunity for public comment on the proposed collection of certain information by the agency. Under the Paperwork Reduction Act of 1995 (the PRA), Federal agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing information collection, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the reporting requirements for the collection ‘‘Recommended Glossary and Educational Outreach to Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use.’’ DATES: Submit written or electronic comments on the collection of information by October 30, 2007. PO 00000 Frm 00052 Fmt 4703 Sfmt 4703 50373 Submit electronic comments on the collection of information to: https://www.fda.gov/ dockets/ecomments or https:// www.regulations.gov. Submit written comments on the collection of information to the Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, rm. 1061, Rockville, MD 20852. All comments should be identified with the docket number found in brackets in the heading of this document. ADDRESSES: FOR FURTHER INFORMATION CONTACT: Denver Presley, Jr., Office of Chief Information Officer (HFA–250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301–827– 1472. Under the 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. ‘‘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 provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, before submitting the collection to OMB for approval. To comply with this requirement, FDA is publishing notice of the proposed collection of information set forth in this document. SUPPLEMENTARY INFORMATION: With respect to the following collection of information, FDA invites comments on these topics: (1) Whether the proposed collection of information is necessary for the proper performance of FDA’s functions, including whether the information will have practical utility; (2) the accuracy of FDA’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; (3) ways to enhance the quality, utility, and clarity of the information to be collected; and (4) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques, when appropriate, and other forms of information technology. E:\FR\FM\31AUN1.SGM 31AUN1

Agencies

[Federal Register Volume 72, Number 169 (Friday, August 31, 2007)]
[Notices]
[Pages 50372-50373]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-17351]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Medicare & Medicaid Services

[Document Identifier: CMS-10249 and CMS-10120]


Agency Information Collection Activities; Proposed Collection; 
Comment Request

AGENCY: Centers for Medicare & 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 & Medicaid 
Services (CMS) 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.
    1. Type of Information Collection Request: New Collection; Title of 
Information Collection: Administrative Requirements for section 6071 of 
the Deficit Reduction Act of 2005 (DRA); Use: CMS will use an 
Operational Protocol Instruction Guide and template for the development 
of Operational Protocols for the States selected to participate in the 
Money Follows the Person (MFP) Rebalancing Demonstration. The guide 
will provide instruction on the required elements of the State's 
Operational Protocol, which must be submitted and approved before a 
State may enroll individuals in the State's demonstration program or 
begin to claim service dollars. The DRA Section 6071(c)(9) requires the 
States to provide information and assurances that total expenditures 
under the State Medicaid program for home and community-based long-term 
care services will not be less for any fiscal year during the MFP 
demonstration project than for the greater of such expenditures for 
fiscal year 2005 or any succeeding fiscal year before the first of the 
year of the MFP demonstration project. Accordingly, States are required 
to submit Maintenance of Effort (MOE) forms and MFP Budget forms on an 
annual basis. Additionally, in order to receive enhanced FMAP, States 
are required to submit the MFP Demonstration Financial Forms on a 
quarterly basis. Section 6071(g) of the DRA requires a national 
evaluation of the MFP demonstration project and a final report to the 
President and Congress. For the national evaluation, States will be 
required to submit semi-annual reports that describe their progress in 
implementing their MFP programs and rebalancing their long-term care 
systems. In addition, States will be required to submit on a quarterly 
basis an MFP Finders File, which will include eligibility records for 
all MFP participants, and an MFP Services File, which will include 
records for each service funded with MFP grant funds. Form Number: CMS-
10249 (OMB: 0938-NEW); Frequency: Reporting--Yearly, 
Quarterly, Semi-annually and Once; Affected Public: States, Local or 
Tribal Governments; Number of Respondents: 31; Total Annual Responses: 
229.4; Total Annual Hours: 7,843.
    2. Type of Information Collection Request: Extension without change 
of a currently approved collection; Title of Information Collection: 
1932 State Plan Amendment Template, State Plan Requirements and 
Supporting Regulations in 42 CFR 438.50; Form No.: CMS-10120 
(OMB 0938-0933); Use: The State Medicaid Agencies will 
complete the template. CMS will review the information to determine if 
the State has met all the requirements under 1932(1)(1)(A) and 42 CFR 
438.50. Once all requirements are met, the State will be allowed to 
enroll Medicaid

[[Page 50373]]

beneficiaries on a mandatory basis into managed care entities without 
section 1115 or 1915(b) waiver authority; Frequency: On occasion; 
Affected Public: State, local, or tribal government; Number of 
Respondents: 56; Total Annual Responses: 10; Total Annual Hours: 100.
    To obtain copies of the supporting statement and any related forms 
for the proposed paperwork collections referenced above, access CMS' 
Web Site address at https://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.
    To be assured consideration, comments and recommendations for the 
proposed information collections must be received at the address below, 
no later than 5 p.m. on October 30, 2007.

CMS, Office of Strategic Operations and Regulatory Affairs, Division of 
Regulations Development--A, Attention: Melissa Musotto, Room C4-26-05, 
7500 Security Boulevard, Baltimore, Maryland 21244-1850.

    Dated: August 24, 2007.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations 
and Regulatory Affairs.
[FR Doc. E7-17351 Filed 8-30-07; 8:45 am]
BILLING CODE 4120-01-P
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