Submission for OMB Review; Comment Request, 27071-27072 [2012-10848]
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Federal Register / Vol. 77, No. 89 / Tuesday, May 8, 2012 / Notices
studies, and disseminates information
about existing state and local laws that
may have application to public health;
(3) engages national, state and local
public health partners and policy
makers, state, local, and U.S. court
systems and law enforcement in
identifying priorities and in developing
and applying legal tools; (4) develops
practical, law-centered tools for
practitioners and policy makers at the
STLT levels; and (5) provides
consultation and technical assistance to
CDC programs and partners.
Knowledge Management Office
(CQA5). (1) Facilitates the development
and provision of training and
development opportunities to STLT
health partners; (2) provides leadership
in identifying and implementing
strategies for effective collaboration of
CDC and STLT public health
professionals; (3) works collaboratively
across OSTLTS, CDC and STLT agencies
to disseminate and promote the
adoption of leading practices, lessons
learned and models that improve
community programs; and (4)
established collaboration and
coordination between clinical medicine
and public health to better coordinate
and partner for healthier communities.
Field Services Office (CQA4). (1)
Provides cross-agency support, guidance
and strategic direction for the
recruitment, development, and
management of CDC field staff
embedded within external public health
agencies; (2) develops and provides
training for project officers and
consultants, grants management
officials, field staff and leadership; (3)
conducts periodic assessments of field
staff and project officer needs; (4)
maintains accurate demographic and
assignment-related data on field staff;
(5) supports grants management
optimization efforts to improve SILT
health agencies; (6) provides agencywide leadership and coordination in the
identification, assessment, and
development of solutions to improve
CDC technical assistance and service
delivery; (7) assists in the coordination
of CDC and OSTLTS Director site visits
to SILT agencies; and (8) manages the
Public Health Associates Program and
provides direct oversight and
supervision for the Associates.
Division of Public Health Performance
Improvement (CQB). The mission of the
Division of Public Health Performance
Improvement (DPHPI) is to advance U.S.
public health agency and system
performance to better serve and protect
the population. In carrying out its
mission, DPHPI: (1) Promotes
coordination among federal and SILT
health agencies to support the
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improvement and development of
organizations and enable evidencebased policy and decision making; (2)
identifies and evaluates gaps in the
structure and operation of public health
agencies and systems; (3) forecasts
emerging opportunities and challenges
to governmental public health agencies/
systems and assists in prioritizing
essential resources to ensure optimal
response; (4) strengthens operational
performance and capability of SILT
health agencies; (5) develops and
disseminates evidence of successful
strategies, organizational structures,
policies, programs, and system
improvements; (6) supports SILT
agencies to meet national standards and
attain accreditation; (7) supports SILT
health agency performance management
and quality improvement activities; and
(8) provides the scientific leadership
and management to ensure the quality
of science within OSTLTS.
Office of the Director (CQB1). (1)
Manages, directs and coordinates the
activities of DPHPI; (2) provides
leadership and guidance on division
operations, policies, program
development and program integration;
(3) coordinates with Federal and STLT
agencies and CDC programs to leverage
cross-cutting activities to develop
stronger organizations and enable
evidence-based policy and decision
making; and (4) provides leadership in
the development and implementation of
evidence-based approaches for public
health system management and
improvement.
Health Department and Systems
Development Branch (CQBB). (1)
Identifies, synthesizes and forecasts
emerging opportunities and challenges
to public health departments and
systems; (2) provides leadership to
prioritize and, develop tools, resources,
standards, and practices to strengthen
operational performance and capability
of STLT health departments with
special emphasis on performance and
quality improvement, and assessment
and planning; (3) supports efforts to use
national accreditation and other
important standards to improve public
health performance, quality, and service
delivery; and (4) provides technical
assistance, expertise, consultation, and
cross-learning opportunities to STLT
health departments.
Applied Systems Research and
Evaluation Branch (CQBC). (1) Engages
in research to identify gaps in the
structure and operation of public health
agencies and systems; (2) evaluates and
reports on STLT health outcomes and
other indicators as appropriate to
stimulate improvement activities; (3)
conducts assessments and analysis of
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TLT programs and data to increase
effectiveness and efficiencies; (4)
provides evidence of successful
strategies, organizational structures,
policies, programs, and system
improvements that advance prevention
and health promotion programs and
overall health outcomes; and (5)
evaluates and validates standards,
policies, leading practices, and models
across CDC and STLT agencies.
Dated: April 25, 2012.
Sherri A. Berger,
Chief Operating Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2012–10887 Filed 5–7–12; 8:45 am]
BILLING CODE 4160–18–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Permanency Innovations
Initiative (PII) Evaluation: Phase 1.
OMB No.: New Collection.
Description: The Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS) intends to collect data
for an evaluation of the Permanency
Innovations Initiative (PII). This 5-year
initiative, funded by the Children’s
Bureau (CB) within ACF, is intended to
build the evidence base for innovative
interventions that enhance well-being
and improve permanency outcomes for
particular groups of children and youth
who are at risk for long-term foster care
and who experience the most serious
barriers to timely permanency.
The CB has funded six grantees to
identify local barriers to permanent
placement and implement innovative
strategies that mitigate or eliminate
those barriers and reduce the likelihood
that children will remain in foster care
for three years or longer. The first year
of the initiative focused on clarifying
grantees’ target populations and
intervention programs. In addition,
evaluation plans were developed to
support rigorous site-specific and crosssite studies to document the
implementation and effectiveness of the
grantees’ projects and the initiative
overall.
Data collection for the PII evaluation
includes a number of components being
launched at different points in time. The
purpose of the current document is to
request approval of data collection
efforts needed for a first phase of data
collection and to request a waiver for
E:\FR\FM\08MYN1.SGM
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27072
Federal Register / Vol. 77, No. 89 / Tuesday, May 8, 2012 / Notices
subsequent 60 day notices for later
components of the evaluation. The first
phase includes data collection for a
cross-site implementation study and
site-specific impact evaluations in two
PIT grantee sites (Kansas; Washoe
County, Nevada) that will begin
implementing interventions during the
second year of the PII grant period. The
second phase includes a cross-site cost
evaluation and site-specific impact
evaluations in four PII grantee sites
expected to implement interventions in
the third year of the PII grant period.
Data for the cross-site implementation
study will be collected through: (1)
Interviews with grantee staff and key
informants conducted by telephone and
during site visits; (2) web-based
instruments completed by grantee staff
and key informants; and (3) retrieval
and submission of aggregate data from
grantee data systems. Data for the
Kansas impact evaluation will be
collected through (1) family
assessments; (2) caseworkers’ clinical
assessments of children and families;
and (3) caseworker discussions. Data for
the Washoe County impact evaluation
will be collected through family
assessments.
Respondents: Families (parents, or
permanent or foster caregivers;
children), caseworkers, supervisors,
service providers, and key informants
such as grantee project directors, data
managers, and representatives of partner
agencies.
ANNUAL BURDEN ESTIMATES
Annual
number of respondents
Instrument
Number of
responses per
respondent
60
150
30
2
—
1
2
4
8
—
0.3
0.8
2.0
1.5
—
18
240
240
24
522
300
300
4
4
—
1
3
150
150
—
0.1
1.5
1.0
0.5
—
30
1350
600
300
2280
175
—
2
—
1.5
—
525
525
srobinson on DSK4SPTVN1PROD with NOTICES
CROSS-SITE IMPLEMENTATION STUDY:
Survey of Organization/System Readiness .....................................................
Implementation Drivers Web Survey ...............................................................
Grantee Case Study Protocol ..........................................................................
Fidelity Data (Implementation Quotient Tracker) .............................................
Cross-Site Estimated Total ..............................................................................
KANSAS:
Caregiver Initial Information Form ............................................................
Family Assessment Battery ......................................................................
CAFAS/PECFAS ......................................................................................
Caseworker Discussions for NCFAS–G&R Completion ..................................
Kansas Estimated Total ...................................................................................
WASHOE COUNTY:
Family Assessment Battery ......................................................................
Washoe Estimated Total ..........................................................................
Estimated Total Annual Burden
Hours: 3327.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
L’Enfant Promenade SW., Washington,
DC 20447, Attn: OPRE Reports
Clearance Officer. All requests should
be identified by the title of the
information collection. Email address:
OPREinfocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email:
OIRA_SUBMISSION@OMB.EOP.GOV,
Attn: Desk Officer for the
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17:33 May 07, 2012
Jkt 226001
Administration, for Children and
Families.
Steven M. Hanmer,
OPRE Reports Clearance Officer.
[FR Doc. 2012–10848 Filed 5–7–12; 8:45 am]
BILLING CODE 4184–01–M
Average
burden hours
per response
Total annual
burden hours
information which negated the necessity
for the planned meeting. The Agency
intends to continue evaluating NDA
200–436 and, as needed, may schedule
an Advisory Committee meeting in the
future.
FOR FURTHER INFORMATION CONTACT:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2012–N–0001]
Gastrointestinal Drugs Advisory
Committee; Cancellation
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The meeting of the
Gastrointestinal Drugs Advisory
Committee scheduled for May 31, 2012,
is canceled. This meeting was
announced in the Federal Register of
March 23, 2012 (77 FR 17078). The
meeting is being canceled because the
Agency no longer needs to discuss the
issues that were originally under
consideration in the review of the
application. The sponsor of the new
drug application (NDA) submitted new
SUMMARY:
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Minh Doan, Center for Drug Evaluation
and Research, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 31, rm. 2417, Silver Spring,
MD 20993–0002, 301–796–9001, Fax:
301–847–8533, email:
GIDAC@fda.hhs.gov, or FDA Advisory
Committee Information Line, 1–800–
741–8138 (301–443–0572 in the
Washington, DC area), to find out
further information regarding FDA
advisory committee information or visit
our Web site at https://www.fda.gov/
AdvisoryCommittees/default.htm.
Dated: May 2, 2012.
Jill Hartzler Warner,
Acting Associate Commissioner for Special
Medical Programs.
[FR Doc. 2012–10990 Filed 5–7–12; 8:45 am]
BILLING CODE 4160–01–P
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Agencies
[Federal Register Volume 77, Number 89 (Tuesday, May 8, 2012)]
[Notices]
[Pages 27071-27072]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-10848]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Permanency Innovations Initiative (PII) Evaluation: Phase 1.
OMB No.: New Collection.
Description: The Administration for Children and Families (ACF),
U.S. Department of Health and Human Services (HHS) intends to collect
data for an evaluation of the Permanency Innovations Initiative (PII).
This 5-year initiative, funded by the Children's Bureau (CB) within
ACF, is intended to build the evidence base for innovative
interventions that enhance well-being and improve permanency outcomes
for particular groups of children and youth who are at risk for long-
term foster care and who experience the most serious barriers to timely
permanency.
The CB has funded six grantees to identify local barriers to
permanent placement and implement innovative strategies that mitigate
or eliminate those barriers and reduce the likelihood that children
will remain in foster care for three years or longer. The first year of
the initiative focused on clarifying grantees' target populations and
intervention programs. In addition, evaluation plans were developed to
support rigorous site-specific and cross-site studies to document the
implementation and effectiveness of the grantees' projects and the
initiative overall.
Data collection for the PII evaluation includes a number of
components being launched at different points in time. The purpose of
the current document is to request approval of data collection efforts
needed for a first phase of data collection and to request a waiver for
[[Page 27072]]
subsequent 60 day notices for later components of the evaluation. The
first phase includes data collection for a cross-site implementation
study and site-specific impact evaluations in two PIT grantee sites
(Kansas; Washoe County, Nevada) that will begin implementing
interventions during the second year of the PII grant period. The
second phase includes a cross-site cost evaluation and site-specific
impact evaluations in four PII grantee sites expected to implement
interventions in the third year of the PII grant period.
Data for the cross-site implementation study will be collected
through: (1) Interviews with grantee staff and key informants conducted
by telephone and during site visits; (2) web-based instruments
completed by grantee staff and key informants; and (3) retrieval and
submission of aggregate data from grantee data systems. Data for the
Kansas impact evaluation will be collected through (1) family
assessments; (2) caseworkers' clinical assessments of children and
families; and (3) caseworker discussions. Data for the Washoe County
impact evaluation will be collected through family assessments.
Respondents: Families (parents, or permanent or foster caregivers;
children), caseworkers, supervisors, service providers, and key
informants such as grantee project directors, data managers, and
representatives of partner agencies.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average
Instrument Annual number responses per burden hours Total annual
of respondents respondent per response burden hours
----------------------------------------------------------------------------------------------------------------
CROSS-SITE IMPLEMENTATION STUDY:
Survey of Organization/System Readiness......... 60 1 0.3 18
Implementation Drivers Web Survey............... 150 2 0.8 240
Grantee Case Study Protocol..................... 30 4 2.0 240
Fidelity Data (Implementation Quotient Tracker). 2 8 1.5 24
Cross-Site Estimated Total...................... -- -- -- 522
KANSAS:
Caregiver Initial Information Form.......... 300 1 0.1 30
Family Assessment Battery................... 300 3 1.5 1350
CAFAS/PECFAS................................ 4 150 1.0 600
Caseworker Discussions for NCFAS-G&R Completion. 4 150 0.5 300
Kansas Estimated Total.......................... -- -- -- 2280
WASHOE COUNTY:
Family Assessment Battery................... 175 2 1.5 525
Washoe Estimated Total...................... -- -- -- 525
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 3327.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 370 L'Enfant Promenade
SW., Washington, DC 20447, Attn: OPRE Reports Clearance Officer. All
requests should be identified by the title of the information
collection. Email address: OPREinfocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Email: OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration, for
Children and Families.
Steven M. Hanmer,
OPRE Reports Clearance Officer.
[FR Doc. 2012-10848 Filed 5-7-12; 8:45 am]
BILLING CODE 4184-01-M