Proposed Information Collection Activity; Comment Request, 30031-30032 [2010-12877]

Download as PDF 30031 Federal Register / Vol. 75, No. 103 / Friday, May 28, 2010 / Notices Hours: 5,530. (For policy questions regarding this collection contact Ron Lambert at 410–786–6624. For all other issues call 410–786–1326.) 5. Type of Information Collection Request: Revision of a currently approved collection; Title of Information Collection: Medicare Current Beneficiary Survey; Use: The Medicare Current Beneficiary Survey (MCBS) serves to measure what impact the changes have on the program and its beneficiaries. The MCBS is a comprehensive data collection effort that fills an information gap in the Centers for Medicare and Medicaid Services, and is depended on to help manage the program. Being able to examine various characteristics and to chart evolving trends offers policy makers a reliable tool for making informed decisions. The MCBS is used to identify potential new policy direction or modifications to the Medicare program and once those program enhancements are implemented, monitor the impact of those changes. The central goals of the MCBS are to determine medical care expenditures and sources of payment for all services, including copayments, deductibles, and non-covered services; to ascertain all types of health insurance coverage and relate coverage to actual payments; and to trace processes over time, such as changes in health status, spending down to Medicaid eligibility, and the impacts of program changes. Form Number: CMS–P–0015A (OMB#: 0938–0568); Frequency: Yearly; Affected Public: Business or other for-profits and Not-for-profit institutions; Number of Respondents: 16,217; Total Annual Responses: 48,650; Total Annual Hours: 57,062. (For policy questions regarding this collection contact William Long at 410–786–7927. For all other issues call 410–786–1326.) To obtain copies of the supporting statement and any related forms for the proposed paperwork collections referenced above, access CMS’ Web Site 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. 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 July 27, 2010: 1. Electronically. You may submit your comments electronically to https:// 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. Dated: May 21, 2010. Martique Jones, Director, Regulations Development DivisionB, Office of Strategic Operations and Regulatory Affairs. DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Proposed Projects Title: Child Care and Development Block Grant Reporting Requirements— ACF–700. OMB No.: 0980–0241. Description: The Child Care and Development Fund (CCDF) report requests annual Tribal aggregate information on services provided through the CCDF, which is required by the CCDF Final Rule (45 FR parts 98 and 99). Tribal Lead Agencies (TLAs) are required to submit annual aggregate data appropriate to Tribal programs on children and families receiving CCDFfunded child care services. The CCDF statute and regulations also require TLAs to submit a supplemental narrative as part of the ACF–700 report. This narrative describes child care activities and actions in the TLA’s service area. Information from the ACF– 700 and supplemental narrative report will be included in the Secretary’s Report to Congress, as appropriate, and will be shared with all TLAs to inform them of CCDF-funded activities in other Tribal programs. Respondents: Tribal Governments. [FR Doc. 2010–12624 Filed 5–27–10; 8:45 am] BILLING CODE 4120–01–P ANNUAL BURDEN ESTIMATES Number of respondents Instrument jlentini on DSKJ8SOYB1PROD with NOTICES ACF–700 Report .............................................................................................. Estimated Total Annual Burden Hours: 9,880. 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 VerDate Mar<15>2010 17:43 May 27, 2010 Jkt 220001 260 Families, Office of Administration, Office of Information Services, 370 L’Enfant Promenade, SW., Washington, 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 PO 00000 Frm 00065 Fmt 4703 Sfmt 4703 Number of responses per respondent 1 Average burden hours per response 38 Total burden hours 9,880 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) 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 E:\FR\FM\28MYN1.SGM 28MYN1 30032 Federal Register / Vol. 75, No. 103 / Friday, May 28, 2010 / Notices Reports Clearance Officer at (301) 443– 1129. Comments are invited on: (a) The proposed collection of information for the proper performance of the functions of the agency; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) ways to enhance 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. comments and suggestions submitted within 60 days of this publication. Dated: May 25, 2010. Robert Sargis, Reports Clearance Officer. [FR Doc. 2010–12877 Filed 5–27–10; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Comment Request In compliance with the requirement for opportunity for public comment on proposed data collection projects (section 3506(c)(2)(A) of Title 44, United States Code, as amended by the Paperwork Reduction Act of 1995, Pub. L. 104–13), the Health Resources and Services Administration (HRSA) publishes periodic summaries of proposed projects being developed for submission to the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. To request more information on the proposed project or to obtain a copy of the data collection plans and draft instruments, e-mail paperwork@hrsa.gov or call the HRSA Proposed Project: Organ Procurement and Transplantation Network and Scientific Registry of Transplant Recipients Data System (OMB No. 0915–0157)—Extension Section 372 of the Public Health Service (PHS) Act requires that the Secretary, by contract, provide for the establishment and operation of an Organ Procurement and Transplantation Network (OPTN). The OPTN, among other responsibilities, operates and maintains a national waiting list of individuals requiring organ transplants, maintains a computerized system for matching donor organs with transplant candidates on the waiting list, and operates a 24-hour system to facilitate matching organs with individuals included in the list. Number of respondents jlentini on DSKJ8SOYB1PROD with NOTICES Form Deceased Donor Registration .............................................. Death referral data ............................................................... Death Notification Referral—Eligible ................................... Death Notification Referral—Imminent ................................ Living Donor Registration .................................................... Living Donor Follow-up ........................................................ Donor Histocompatibility ...................................................... Recipient Histocompatibility ................................................. Heart Candidate Registration .............................................. Lung Candidate Registration ............................................... Heart/Lung Candidate Registration ..................................... Thoracic Registration ........................................................... Thoracic Follow-up ............................................................... Kidney Candidate Registration ............................................ Kidney Registration .............................................................. Kidney Follow-up * ............................................................... Liver Candidate Registration ............................................... Liver Registration ................................................................. Liver Follow-up ..................................................................... Kidney/Pancreas Candidate Registration ............................ Kidney/Pancreas Registration .............................................. Kidney/Pancreas Follow-up ................................................. Pancreas Candidate Registration ........................................ Pancreas Registration .......................................................... Pancreas Follow-up ............................................................. Intestine Candidate Registration .......................................... Intestine Registration ........................................................... Intestine Follow-up ............................................................... Post Transplant Malignancy ................................................ VerDate Mar<15>2010 17:43 May 27, 2010 Jkt 220001 PO 00000 Frm 00066 Responses per respondents 58 58 58 58 308 308 156 156 127 68 51 127 127 241 241 241 129 129 129 143 143 143 143 143 143 44 44 44 684 Fmt 4703 Sfmt 4703 216 12 161 168 39 50 131 196 35 42 2 36 320 183 83 742 109 58 519 14 7 85 7 3 20 7 5 28 10 Data for the OPTN data system are collected from transplant hospitals, organ procurement organizations, and tissue-typing laboratories. The information is used to indicate the disease severity of transplant candidates, to monitor compliance of member organizations with OPTN rules and requirements, and to report periodically on the clinical and scientific status of organ donation and transplantation in this country. Data are used to develop transplant, donation and allocation policies, to determine if institutional members are complying with policy, to determine member specific performance, to ensure patient safety and to fulfill the requirements of the OPTN Final Rule. The practical utility of the data collection is further enhanced by requirements that the OPTN data must be made available, consistent with applicable laws, for use by OPTN members, the Scientific Registry of Transplant Recipients, the Department of Health and Human Services, and others for evaluation, research, patient information, and other important purposes. No revisions of the 26 data collection forms are proposed at this time; however, the OPTN is currently undergoing a review of the forms and expects to submit proposed revisions within the next year. The annual estimate of burden is as follows: Total responses 12,528 696 9338 9744 12,012 15,400 20,436 30,576 4,445 2,856 102 4,572 40,640 44,103 20,003 178,822 14,061 7,482 66,951 2,002 1,001 12,155 1,001 429 2,860 308 220 1,232 6,840 E:\FR\FM\28MYN1.SGM 28MYN1 Hours per response 0.7500 10.0000 0.2000 0.5000 0.6500 0.5000 0.1000 0.2000 0.5000 0.5000 0.5000 0.7500 0.6500 0.5000 0.7500 0.5500 0.5000 0.6500 0.5000 0.5000 0.9000 0.8500 0.5000 0.7500 0.6500 0.5000 0.9000 0.8500 0.2000 Total burden hours 9,396.00 6,960.00 1,867.60 4,872.00 7,807.80 7,700.00 2,043.60 6,115.20 2,222.50 1,428.00 51.00 3,429.00 26,416.00 22,051.50 15,002.25 98,352.10 7,030.50 4,863.30 33,475.50 1,001.00 900.90 10,331.75 500.50 321.75 1,859.00 154.00 198.00 1,047.20 1,368.00

Agencies

[Federal Register Volume 75, Number 103 (Friday, May 28, 2010)]
[Notices]
[Pages 30031-30032]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-12877]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

Proposed Projects

    Title: Child Care and Development Block Grant Reporting 
Requirements--ACF-700.
    OMB No.: 0980-0241.
    Description: The Child Care and Development Fund (CCDF) report 
requests annual Tribal aggregate information on services provided 
through the CCDF, which is required by the CCDF Final Rule (45 FR parts 
98 and 99). Tribal Lead Agencies (TLAs) are required to submit annual 
aggregate data appropriate to Tribal programs on children and families 
receiving CCDF-funded child care services. The CCDF statute and 
regulations also require TLAs to submit a supplemental narrative as 
part of the ACF-700 report. This narrative describes child care 
activities and actions in the TLA's service area. Information from the 
ACF-700 and supplemental narrative report will be included in the 
Secretary's Report to Congress, as appropriate, and will be shared with 
all TLAs to inform them of CCDF-funded activities in other Tribal 
programs.
    Respondents: Tribal Governments.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                   Instrument                        Number of     responses per     hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
ACF-700 Report..................................             260               1              38           9,880
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 9,880.
    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, 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) 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

[[Page 30032]]

comments and suggestions submitted within 60 days of this publication.

    Dated: May 25, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-12877 Filed 5-27-10; 8:45 am]
BILLING CODE 4184-01-P
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