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