Agency Information Collection Activities: Submission for OMB Review: Comment Request, 74737-74738 [2010-30212]

Download as PDF 74737 Federal Register / Vol. 75, No. 230 / Wednesday, December 1, 2010 / Notices also consistent with the Small Business Regulatory Enforcement Fairness Act of 1996 (Pub. L. 104–121), as outreach activities by government agencies to small businesses. The goal of this public workshop is to present information that will enable manufacturers and regulated industry to better comply with labeling requirements, especially in light of growing concerns about obesity and food allergens. Information presented will be based on Agency position as articulated through regulation, compliance policy guides, and information previously made available to the public. This is a hands-on workshop. Topics to be discussed at the workshop include: (1) Mandatory label elements, (2) nutrition labeling requirements, (3) the Food Allergen Labeling and Consumer Protection Act of 2004, (4) health and nutrient content claims, (5) special labeling issues such as exemptions, and (6) current topics on food labeling and nutrition. FDA expects that participation in this public workshop will provide regulated industry with greater understanding of the Agency’s regulatory and policy perspectives on food labeling and increase voluntary compliance with labeling requirements. Dated: November 24, 2010. Leslie Kux, Acting Assistant Commissioner for Policy. [FR Doc. 2010–30191 Filed 11–30–10; 8:45 am] BILLING CODE 4160–01–P DEPARTMENT OF HEALTH AND HUMAN SERIVCES Health Resources and Services Administration Agency Information Collection Activities: Submission for OMB Review: Comment Request Periodically, the Health Resources and Services Administration (HRSA) publishes abstracts of information collection requests under review by the Office of Management and Budget (OMB), in compliance with the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request a copy of the clearance requests submitted to OMB for review, call the HRSA Reports Clearance Office on (301) 443–1129. The following request has been submitted to OMB for review under the Paperwork Reduction Act of 1995: Proposed Project: Ryan White HIV/ AIDS Program Annual Data Report Form: Data Report Form: (OMB No. 0915–0253)—Extension The Ryan White HIV/AIDS Program Annual Data Report was first implemented in 2002 by HRSA’s HIV/ AIDS Bureau (HAB) as the CARE Act Data Report (CADR). Grantees and their subcontracted service providers who are funded under Parts A, B, C, and D of Title XXVI of the Public Health Service Act, as amended by the Ryan White HIV/AIDS Treatment Extension Act of 2009 (Ryan White HIV/AIDS Program), complete the report. All Parts of the Ryan White HIV/AIDS Program specify HRSA’s responsibilities in the administration of grant funds, the allocation of funds, the evaluation of programs for the population served, and Number of grantee respondents Program under which grantee is funded Part Part Part Part A B C D the improvement of the quantity and quality of care. Accurate records of the providers receiving Ryan White HIV/ AIDS Program funding, the services provided, and the clients served continue to be critical to the implementation of the legislation and thus are necessary for HRSA to fulfill its responsibilities. Ryan White HIV/AIDS Program Grantees are required to report aggregate data to HRSA annually. The Ryan White Data Report (RDR) is completed by grantees and their subcontracted service providers. The Report has seven different sections requesting: (1) Characteristics of the service providers; (2) demographic information about the clients served; (3) information about the type of core and support services provided and the number of clients served; (4) information about HIV counseling and testing services; (5) clinical information about the clients who receive medical care; (6) demographic tables for Parts C and D; and (7) information about the Health Insurance Program. The primary purposes of the Data Report are to: (1) Characterize the organizations where clients receive services; (2) provide information on the number and characteristics of clients who receive Ryan White HIV/AIDS Program Services; and (3) enable HAB to describe the type and amount of services a client receives. In addition to meeting the goal of accountability to the Congress, clients, advocacy groups, and the general public, information collected on the RDR is critical for HRSA, state and local grantees, and individual providers to assess the status of existing HIVrelated service delivery systems. The estimated burden is as follows: Hours to coordinate receipt of data Responses per grantee Total hour burden ............................................................................................................... ............................................................................................................... ............................................................................................................... ............................................................................................................... 56 59 354 98 1 1 1 1 40 40 20 20 2,240 2,360 7,080 1,960 Subtotal ..................................................................................................... 567 ........................ ........................ 13,640 Responses per provider Hours per response Number of provider respondents jlentini on DSKJ8SOYB1PROD with NOTICES Program under which provider is funded Total hour burden Part A only ....................................................................................................... Part B only ....................................................................................................... Part C only ....................................................................................................... Part D only ....................................................................................................... Multiply funded ................................................................................................. 685 558 95 59 683 1 1 1 1 1 26 26 44 42 50 17,810 14,508 4,180 2,478 34,150 Subtotal ..................................................................................................... 2,080 ........................ ........................ 73,126 VerDate Mar<15>2010 20:11 Nov 30, 2010 Jkt 223001 PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 E:\FR\FM\01DEN1.SGM 01DEN1 74738 Federal Register / Vol. 75, No. 230 / Wednesday, December 1, 2010 / Notices Number of respondents Total for Both Grantees & Providers ............................................................... Written comments and recommendations concerning the proposed information collection should be sent within 30 days of this Federal Register Notice to the desk officer for HRSA, either by e-mail to OIRA— submission@omb.eop.gov or by fax to 202–395–6974. Please direct all correspondence to the ‘‘attention of the desk officer for HRSA.’’ Dated: November 24, 2010. Robert Hendricks, Director, Division of Policy and Information Coordination. [FR Doc. 2010–30212 Filed 11–30–10; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Proposed Collection; Comment Request; Online Skills Training for PCPs on Substance Abuse Under the provisions of Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institute on Drug Abuse, the National Institutes of Health has submitted to the Office of Management and Budget (OMB) a request to review and approve the information collection listed below. This proposed information collection was previously published in the Federal SUMMARY: Total hour burden 2,647 ........................ Register in Vol. 75 No. 144, pages 44265–44266, on July 28, 2010 and allowed 60 days for public comment. One public comment was received on the instruments outlined in the 60-day notice. A response to this request was sent to the interested party. The purpose of this notice is to allow an additional 30 days for public comment. 5 CFR 1320.5 (General requirements) Reporting and Recordkeeping Requirements: Final Rule requires that the agency inform the potential persons who are to respond to the collection of information that such persons are not required to respond to the collection of information unless it displays a currently valid OMB control number. Proposed Collection: Title: Online Skills Training for PCPs on Substance Abuse. Type of Information Collection Request: New. Need and Use of Information Collection: This research will evaluate the effectiveness of the Online Skills Training for PCPs on Substance Abuse, via the Web site SBIRTTraining.com, to positively impact the knowledge, attitudes, intended behaviors and clinical skills of primary care physicians in the US who treat substance abuse patients. The Online Skills Training for PCPs on Substance Abuse is a new program developed with funding from the National Institute on Drug Abuse. The primary goal is to assess the impact ........................ 86,766 of the training program on knowledge, attitude, intended behavior, and clinical skills. A secondary goal is to assess learner satisfaction with the program. If the program is a success, there will be a new, proven resource available to primary care physicians to improve their ability to assess and treat substance use disorders. In order to evaluate the effectiveness of the program, information will be collected from primary care physicians before exposure to the Web based materials (pre-test), after exposure to the Web based materials (post-test), and 4–6 weeks after the program has been completed (follow-up). Frequency of Response: On occasion. Affected Public: Primary care physicians who treat patients who have substance abuse. Type of Respondents: Physicians. The annual reporting burden is as follows: Estimated Number of Respondents: 80. Estimated Number of Responses per Respondent: 3. Average Burden Hours per Response: 0.75. Estimated Total Annual Burden Hours Requested: 180. The Annualized Cost to Respondents Is Estimated at: $13,500. There are no Capital Costs, Operating Costs, and/or Maintenance Costs to report. Estimated number of respondents Estimated number of responses per respondent Average burden hours per response Estimated annual burden hours requested Primary care physicians .......................................................................... jlentini on DSKJ8SOYB1PROD with NOTICES Type of respondents 80 3 0.75 180 Request for Comments: Written comments and/or suggestions from the public and affected agencies are invited on one or more of the following points: (1) Whether the proposed collection of information is necessary for the proper performance of the function of the agency, including whether the information will have practical utility; (2) The accuracy of the agency’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 VerDate Mar<15>2010 20:11 Nov 30, 2010 Jkt 223001 collection of information on those who are to respond, including the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology. Direct Comments to OMB: Written comments and/or suggestions regarding the item(s) contained in this notice, especially regarding the estimated public burden and associated response time, should be directed to the: Office of Management and Budget, Office of Regulatory Affairs, OIRA submission@omb.eop.gov or by fax to 202–395–6974, Attention: Desk Officer for NIH. To request more information on PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 the proposed project or to obtain a copy of the data collection plans and instruments, contact: Quandra Scudder, Project Officer, NIH/NIDA/CCTN, Room 3105, MSC 9557, 6001 Executive Boulevard, Bethesda, MD 20892–9557 or email your request, including your address to: scudderq@nida.nih.gov. Comments Due Date: Comments regarding this information collection are best assured of having their full effect if received within 30 days of the date of this publication. E:\FR\FM\01DEN1.SGM 01DEN1

Agencies

[Federal Register Volume 75, Number 230 (Wednesday, December 1, 2010)]
[Notices]
[Pages 74737-74738]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-30212]


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DEPARTMENT OF HEALTH AND HUMAN SERIVCES

Health Resources and Services Administration


Agency Information Collection Activities: Submission for OMB 
Review: Comment Request

    Periodically, the Health Resources and Services Administration 
(HRSA) publishes abstracts of information collection requests under 
review by the Office of Management and Budget (OMB), in compliance with 
the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35). To request 
a copy of the clearance requests submitted to OMB for review, call the 
HRSA Reports Clearance Office on (301) 443-1129. The following request 
has been submitted to OMB for review under the Paperwork Reduction Act 
of 1995:

Proposed Project: Ryan White HIV/AIDS Program Annual Data Report Form: 
Data Report Form: (OMB No. 0915-0253)--Extension

    The Ryan White HIV/AIDS Program Annual Data Report was first 
implemented in 2002 by HRSA's HIV/AIDS Bureau (HAB) as the CARE Act 
Data Report (CADR). Grantees and their subcontracted service providers 
who are funded under Parts A, B, C, and D of Title XXVI of the Public 
Health Service Act, as amended by the Ryan White HIV/AIDS Treatment 
Extension Act of 2009 (Ryan White HIV/AIDS Program), complete the 
report. All Parts of the Ryan White HIV/AIDS Program specify HRSA's 
responsibilities in the administration of grant funds, the allocation 
of funds, the evaluation of programs for the population served, and the 
improvement of the quantity and quality of care. Accurate records of 
the providers receiving Ryan White HIV/AIDS Program funding, the 
services provided, and the clients served continue to be critical to 
the implementation of the legislation and thus are necessary for HRSA 
to fulfill its responsibilities. Ryan White HIV/AIDS Program Grantees 
are required to report aggregate data to HRSA annually. The Ryan White 
Data Report (RDR) is completed by grantees and their subcontracted 
service providers. The Report has seven different sections requesting: 
(1) Characteristics of the service providers; (2) demographic 
information about the clients served; (3) information about the type of 
core and support services provided and the number of clients served; 
(4) information about HIV counseling and testing services; (5) clinical 
information about the clients who receive medical care; (6) demographic 
tables for Parts C and D; and (7) information about the Health 
Insurance Program. The primary purposes of the Data Report are to: (1) 
Characterize the organizations where clients receive services; (2) 
provide information on the number and characteristics of clients who 
receive Ryan White HIV/AIDS Program Services; and (3) enable HAB to 
describe the type and amount of services a client receives. In addition 
to meeting the goal of accountability to the Congress, clients, 
advocacy groups, and the general public, information collected on the 
RDR is critical for HRSA, state and local grantees, and individual 
providers to assess the status of existing HIV-related service delivery 
systems.
    The estimated burden is as follows:

----------------------------------------------------------------------------------------------------------------
                                                                                     Hours to
                                                     Number of     Responses per    coordinate      Total hour
      Program under which grantee is funded           grantee         grantee       receipt of        burden
                                                    respondents                        data
----------------------------------------------------------------------------------------------------------------
Part A..........................................              56               1              40           2,240
Part B..........................................              59               1              40           2,360
Part C..........................................             354               1              20           7,080
Part D..........................................              98               1              20           1,960
 
    Subtotal....................................             567  ..............  ..............          13,640
----------------------------------------------------------------------------------------------------------------


----------------------------------------------------------------------------------------------------------------
                                                     Number of
     Program under which provider is funded          provider      Responses per     Hours per      Total hour
                                                    respondents      provider        response         burden
----------------------------------------------------------------------------------------------------------------
Part A only.....................................             685               1              26          17,810
Part B only.....................................             558               1              26          14,508
Part C only.....................................              95               1              44           4,180
Part D only.....................................              59               1              42           2,478
Multiply funded.................................             683               1              50          34,150
 
    Subtotal....................................           2,080  ..............  ..............          73,126
----------------------------------------------------------------------------------------------------------------


[[Page 74738]]


----------------------------------------------------------------------------------------------------------------
                                                     Number of                                      Total hour
                                                    respondents                                       burden
----------------------------------------------------------------------------------------------------------------
Total for Both Grantees & Providers.............           2,647  ..............  ..............          86,766
----------------------------------------------------------------------------------------------------------------

    Written comments and recommendations concerning the proposed 
information collection should be sent within 30 days of this Federal 
Register Notice to the desk officer for HRSA, either by e-mail to 
OIRA-- submission@omb.eop.gov or by fax to 202-395-6974. Please direct 
all correspondence to the ``attention of the desk officer for HRSA.''

    Dated: November 24, 2010.
Robert Hendricks,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-30212 Filed 11-30-10; 8:45 am]
BILLING CODE 4165-15-P