Agency Information Collection Activities: Proposed Collection: Comment Request, 58392-58393 [2010-23929]

Download as PDF 58392 Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices ESTIMATE OF ANNUALIZED BURDEN HOURS Number of respondents Number of responses per respondent Average burden per response (in hours) Screening Questionnaire ............. 60 1 5/60 5 Pre-exposure Questionnaire ....... 50 1 10/60 8 Post-exposure Questionnaire ...... 50 4 10/60 33 ...................................................... ........................ ........................ .................... 46 Respondents Form name Catfish farm workers ...................................... Total ........................................................ Dated: September 20, 2010. Thelma E. Sims, Acting Reports Clearance Officer, Centers for Disease Control and Prevention. [FR Doc. 2010–24021 Filed 9–23–10; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Substance Abuse and Mental Health Services Administration Agency Information Collection Activities: Submission for OMB Review; Comment Request Periodically, the Substance Abuse and Mental Health Services Administration (SAMHSA) will publish a summary of information collection requests under OMB review, in compliance with the Paperwork Reduction Act (44 U.S.C. Chapter 35). To request a copy of these documents, call the SAMHSA Reports Clearance Officer on (240) 276–1243. Project: Voluntary Customer Satisfaction Surveys To Implement Executive Order 12862 in the Substance Abuse and Mental Health Services Administration (SAMHSA)—(OMB No. 0930–0197)—Extension Executive Order 12862 directs agencies that ‘‘provide significant services directly to the public’’ to ‘‘survey customers to determine the kind and quality of services they want and their level of satisfaction with existing services.’’ SAMHSA provides significant services directly to the public, including treatment providers and State substance abuse and mental health agencies, through a range of mechanisms, including publications, training, meetings, technical assistance and Web sites. Many of these services are focused on information dissemination activities. Number of respondents Type of data collection Total burden hours The purpose of this submission is to extend the existing generic approval for such surveys. The primary use for information gathered is to identify strengths and weaknesses in current service provisions by SAMHSA and to make improvements that are practical and feasible. Several of the customer satisfaction surveys expected to be implemented under this approval will provide data for measurement of program effectiveness under the Government Performance and Results Act (GPRA). Information from these customer surveys will be used to plan and redirect resources and efforts to improve or maintain a high quality of service to health care providers and members of the public. Focus groups may be used to develop the survey questionnaire in some instances. The estimated annual hour burden is as follows: Responses/ respondent Hours/ response Total hours 250 89,750 1 1 2.50 .250 625 22,438 Total .......................................................................................................... srobinson on DSKHWCL6B1PROD with NOTICES Focus groups ................................................................................................... Self-administered, mail, telephone and e-mail surveys ................................... 90,000 ........................ ........................ 23,063 Written comments and recommendations concerning the proposed information collection should be sent by October 25, 2010 to: SAMHSA Desk Officer, Human Resources and Housing Branch, Office of Management and Budget, New Executive Office Building, Room 10235, Washington, DC 20503; due to potential delays in OMB’s receipt and processing of mail sent through the U.S. Postal Service, respondents are encouraged to submit comments by fax to: 202–395– 7285. Dated: September 16, 2010. Elaine Parry, Director, Office of Management, Technology and Operations. [FR Doc. 2010–23932 Filed 9–23–10; 8:45 am] BILLING CODE 4162–20–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 VerDate Mar<15>2010 16:12 Sep 23, 2010 Jkt 220001 PO 00000 Frm 00046 Fmt 4703 Sfmt 4703 (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 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 E:\FR\FM\24SEN1.SGM 24SEN1 58393 Federal Register / Vol. 75, No. 185 / Friday, September 24, 2010 / Notices 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. Proposed Project: Ryan White HIV/ AIDS Treatment Modernization Act of 2006: Data Report Form: (OMB No. 0915–0253)—Extension The Ryan White HIV/AIDS Program Annual Data Report (or the Ryan White Data Report, formerly called the CARE Act Data Report [CADR]) was initially created in 1999 by HRSA’s HIV/AIDS Bureau. Grantees and their subcontracted service providers who are funded under Parts A, B, C, and D, and the Part F Minority AIDS Initiative of Title XXVI of the Public Health Service Act (the Ryan White HIV/AIDS Program), submit the report, which has been revised to more closely resemble the data requested in the client-level data collection instrument that these grantees and providers are now also required to submit. 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. Because client-level data reporting requirements are relatively new for the Ryan White HIV/AIDS Program grantees, the grantees are still required to report aggregate data in the Ryan White Data Report to HRSA annually. The more mature aggregate reporting requirements provide accurate records of the providers receiving Ryan White HIV/AIDS Program funding, the services provided, and the clients served, which continue to be critical to the implementation of the legislation and necessary for HRSA to fulfill its responsibilities. The Ryan White Data Report has seven different sections containing information about the service providers; demographic information about the clients served; information about the type of core and support Number of respondents Program under which grantee is funded Part Part Part Part A B C D services provided and the number of clients served; information about counseling and testing services; clinical information about clients who received outpatient/ambulatory medical care; demographic tables for Parts C and D; and information about health insurance services. The primary purposes of the Ryan White 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 Congress, clients, advocacy groups, and the general public, information collected in the Ryan White Data Report is critical for HRSA, State and local grantees, and individual providers to assess the status of existing HIV-related service delivery systems. The response burden for grantees is estimated as: Responses per grantee Hours per hours Total response 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 hours The response burden for service providers is estimated as: Number of respondents Program under which provider is funded Total response burden 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 Total for Both Grantees & Providers ................................................. srobinson on DSKHWCL6B1PROD with NOTICES Part A Only ...................................................................................................... Part B Only ...................................................................................................... Part C Only ...................................................................................................... Part D Only ...................................................................................................... Funded under more than one program ........................................................... 2,647 ........................ ........................ 86,766 E-mail comments to paperwork@hrsa.gov or mail the HRSA Reports Clearance Officer, Room 10–33, Parklawn Building, 5600 Fishers Lane, Rockville, MD 20857. Written comments should be received within 60 days of this notice. Dated: September 20, 2010. Sahira Rafiullah, Director, Division of Policy and Information Coordination. [FR Doc. 2010–23929 Filed 9–23–10; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [30-Day–10–0215] Agency Forms Undergoing Paperwork Reduction Act Review The Centers for Disease Control and Prevention (CDC) publishes a list of VerDate Mar<15>2010 16:12 Sep 23, 2010 Jkt 220001 PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 E:\FR\FM\24SEN1.SGM 24SEN1

Agencies

[Federal Register Volume 75, Number 185 (Friday, September 24, 2010)]
[Notices]
[Pages 58392-58393]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-23929]


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

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 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

[[Page 58393]]

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.

Proposed Project: Ryan White HIV/AIDS Treatment Modernization Act of 
2006: Data Report Form: (OMB No. 0915-0253)--Extension

    The Ryan White HIV/AIDS Program Annual Data Report (or the Ryan 
White Data Report, formerly called the CARE Act Data Report [CADR]) was 
initially created in 1999 by HRSA's HIV/AIDS Bureau. Grantees and their 
subcontracted service providers who are funded under Parts A, B, C, and 
D, and the Part F Minority AIDS Initiative of Title XXVI of the Public 
Health Service Act (the Ryan White HIV/AIDS Program), submit the 
report, which has been revised to more closely resemble the data 
requested in the client-level data collection instrument that these 
grantees and providers are now also required to submit. 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. Because client-level data reporting 
requirements are relatively new for the Ryan White HIV/AIDS Program 
grantees, the grantees are still required to report aggregate data in 
the Ryan White Data Report to HRSA annually. The more mature aggregate 
reporting requirements provide accurate records of the providers 
receiving Ryan White HIV/AIDS Program funding, the services provided, 
and the clients served, which continue to be critical to the 
implementation of the legislation and necessary for HRSA to fulfill its 
responsibilities. The Ryan White Data Report has seven different 
sections containing information about the service providers; 
demographic information about the clients served; information about the 
type of core and support services provided and the number of clients 
served; information about counseling and testing services; clinical 
information about clients who received outpatient/ambulatory medical 
care; demographic tables for Parts C and D; and information about 
health insurance services.
    The primary purposes of the Ryan White 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 Congress, clients, advocacy 
groups, and the general public, information collected in the Ryan White 
Data Report is critical for HRSA, State and local grantees, and 
individual providers to assess the status of existing HIV-related 
service delivery systems.
    The response burden for grantees is estimated as:

----------------------------------------------------------------------------------------------------------------
                                                     Number of     Responses per     Hours per    Total response
      Program under which grantee is funded         respondents       grantee          hours          burden
----------------------------------------------------------------------------------------------------------------
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
----------------------------------------------------------------------------------------------------------------

    The response burden for service providers is estimated as:

----------------------------------------------------------------------------------------------------------------
                                                     Number of     Responses per     Hours per    Total response
     Program under which provider is funded         respondents      provider          hours          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
Funded under more than one program..............             683               1              50          34,150
                                                 ---------------------------------------------------------------
    Subtotal....................................           2,080  ..............  ..............          73,126
                                                 ---------------------------------------------------------------
        Total for Both Grantees & Providers.....           2,647  ..............  ..............          86,766
----------------------------------------------------------------------------------------------------------------

    E-mail comments to paperwork@hrsa.gov or mail the HRSA Reports 
Clearance Officer, Room 10-33, Parklawn Building, 5600 Fishers Lane, 
Rockville, MD 20857. Written comments should be received within 60 days 
of this notice.

    Dated: September 20, 2010.
Sahira Rafiullah,
Director, Division of Policy and Information Coordination.
[FR Doc. 2010-23929 Filed 9-23-10; 8:45 am]
BILLING CODE 4165-15-P