Agency Information Collection Activities: Proposed Collection: Public Comment Request, 36537-36539 [2014-15051]
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Federal Register / Vol. 79, No. 124 / Friday, June 27, 2014 / Notices
it against unauthorized use or
disclosure. The Privacy Act requires
that personal information be secured
against potential misuse by
unauthorized persons (5 U.S.C.
552a(e)(10)). The Federal Information
Security Management Act of 2002
(FISMA), enacted as Title III of the EGovernment Act of 2002 (44 U.S.C. 3541
et seq.), requires that agencies protect
data and information systems from
unauthorized use, disclosure,
disruption, modification and
destruction, in order to preserve data
integrity, confidentiality, and
availability.
2. ‘‘Disclosure may be made to the
National Archives and Records
Administration and/or the General
Services Administration for the purpose
of records management inspections
conducted under authority of 44 U.S.C.
2904 and 2906.’’
This routine use is necessary to
enable the National Archives and
Records Administration (NARA) and/or
the General Services Administration
(GSA) to carry out records management
functions.
3. ‘‘Disclosure may be made to
contractors and other persons who
perform services for the agency related
to this system of records and who need
access to the records to perform those
services. Recipients shall be required to
comply with the requirements of the
Privacy Act of 1974, as amended, 5
U.S.C. 552a.’’
Where FDA engages a contractor to
carry out a function related to a system
of records, this routine use permits
disclosure to those individuals who
require access to the records in order to
perform the contracted work. The
routine use is necessary to enable FDA
to function in an effective and
coordinated fashion. Additionally, OMB
directs agencies to include such a
routine use for disclosure to contractor
personnel (Appendix I to OMB Circular
A–130—Federal Agency
Responsibilities for Maintaining
Records About Individuals, available at
https://www.whitehouse.gov/omb/
circulars_a130_a130trans4). FDA will
require that individuals to whom
records are disclosed comply with the
information handling obligations
imposed on Federal Agencies by the
Privacy Act.
4. ‘‘When a record on its face, or in
conjunction with other records,
indicates a violation or potential
violation of law, whether civil, criminal,
or regulatory in nature, disclosure may
be made to the appropriate public
authority, whether federal, foreign,
state, local, or tribal, or otherwise,
responsible for enforcing, investigating
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15:30 Jun 26, 2014
Jkt 232001
or prosecuting such violation, if the
information disclosed is relevant to the
responsibilities of the agency or public
authority.’’
When a record in an agency system of
records by itself or in combination with
other records indicates a violation of
law, this routine use allows FDA to
provide the record to the appropriate
law enforcement entity in order to
maintain the integrity of the program
and ensure trust in the system.
5. ‘‘In the event HHS/FDA deems it
desirable or necessary, in determining
whether particular records are required
to be disclosed under the Freedom of
Information Act, disclosure may be
made to the Department of Justice for
the purpose of obtaining its advice.’’
DOJ is the lead Agency on Federal
implementation of the Freedom of
Information Act (FOIA). This routine
use enables FDA to share Privacy Act
records with DOJ to effectively consult
with DOJ regarding the potential
disclosure of the records under the
FOIA as permitted under the relevant
provision of the Privacy Act, 5 U.S.C.
552a(b)(2).
B. FDA Systems of Records Notices to
Which New Routine Uses Will Be Added
FDA will add the specified routine
uses to the remaining FDA SORNs that
do not already contain the same or
similar provisions. A list of these
SORNs is as follows:
09–10–0002 Regulated Industry
Employee Enforcement Records.
09–10–0003 FDA Credential Holder
File.
09–10–0004 Communications (Oral
and Written) With the Public.
09–10–0005 State Food and Drug
Official File.
09–10–0009 Special Studies and
Surveys on FDA-Regulated
Products. Only the first, second,
fourth, and fifth routine uses
described in this document will be
added to this SORN. It already
contains a routine use covering
disclosure to contractors who
perform services for FDA.
09–10–0010 Bioresearch Monitoring
Information System. Only the
second, fourth, and fifth routine
uses described in this document
will be added to this SORN. It
already contains the routine uses
regarding limited disclosure to
contractors and other Agencies.
09–10–0013 Employee Conduct
Investigative Records.
09–10–0018 Employee Identification
Card Information Records.
09–10–0019 Mammography Quality
Standards Act (MQSA) Training
Records.
PO 00000
Frm 00082
Fmt 4703
Sfmt 4703
36537
09–10–0020 FDA Records Related to
Research Misconduct Proceedings.
Only the fifth routine use listed in
this document will be added to this
SORN. It already contains routine
uses that are the same as or similar
to the other four.
09–10–0021 User Fee System. Only
the fourth routine use listed in this
document will be added to this
SORN. It already contains routine
uses that are the same as or similar
to the other four.
III. Comments
Interested persons may submit either
electronic comments regarding this
document to https://www.regulations.gov
or written comments to the Division of
Dockets Management (see ADDRESSES). It
is only necessary to send one set of
comments. Identify comments with the
docket number found in brackets in the
heading of this document. Received
comments may be seen in the Division
of Dockets Management between 9 a.m.
and 4 p.m., Monday through Friday, and
will be posted to the docket at https://
www.regulations.gov.
Dated: June 23, 2014.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2014–15022 Filed 6–26–14; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects (Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995), the
Health Resources and Services
Administration (HRSA) announces
plans to submit an Information
Collection Request (ICR), described
below, to the Office of Management and
Budget (OMB). Prior to submitting the
ICR to OMB, HRSA seeks comments
from the public regarding the burden
estimate, below, or any other aspect of
the ICR.
DATES: Comments on this Information
Collection Request must be received no
later than August 26, 2014.
SUMMARY:
E:\FR\FM\27JNN1.SGM
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36538
Federal Register / Vol. 79, No. 124 / Friday, June 27, 2014 / Notices
Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, Room 10–29, Parklawn
Building, 5600 Fishers Lane, Rockville,
MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call the HRSA Information Collection
Clearance Officer at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
Title V Maternal and Child Health
Services Block Grant to States Program:
Guidance and Forms for the Title V
Application/Annual Report OMB No.
0915–0172—Revision.
Abstract: HRSA is revising the Title V
Maternal and Child Health Services
Block Grant to States Program:
Guidance and Forms for the Title V
Application/Annual Report. The
Guidance is used annually by the 50
states and nine jurisdictions in applying
for Block Grants under Title V of the
Social Security Act and in preparing the
required Annual Report. In partnership
with the leadership in State Title V
Maternal and Child Health (MCH)
programs as well as with other national
MCH leaders and stakeholders, HRSA’s
Maternal and Child Health Bureau
(MCHB) has been working over the past
year to develop and refine a vision for
transforming the MCH Block Grant to
States Program to better meet current
and future challenges facing our
nation’s mothers and children,
including children with special health
care needs (CSHCN) and their families.
The proposed revisions to the
Application and Annual Reporting
requirements and to the data forms that
are contained in the revised Guidance
reflect this vision.
The aims of the MCH Block Grant to
States Program transformation are
threefold: (1) Reduce burden to states,
(2) maintain state flexibility, and (3)
improve accountability. Revisions to
this edition are intended to enable the
state to tell a more cohesive and
comprehensive Title V story and to
better reflect on the program’s
wreier-aviles on DSK5TPTVN1PROD with NOTICES
ADDRESSES:
leadership role and its contributions to
the state’s public health system in
building improved and expanded
systems of care for the MCH population.
It is recognized that the full extent of the
anticipated burden reduction will be
realized over time as states become
more familiar with the new instructions
and reporting requirements. The burden
estimates presented in the table below
are based on previous burden estimates
and consultations with a few states on
the proposed changes. HRSA plans to
solicit additional information from no
more than nine states to derive more
accurate estimates.
Specific changes to this edition of the
Title V Maternal and Child Health
Services Block Grant to States Program:
Guidance and Forms for the Title V
Application/Annual Report include the
following:
(1) Narrative reporting will be
organized by six population health
domains (i.e., maternal and women’s
health, perinatal health, child health,
CSHCN, adolescent health, and life
course); (2) Revised National
Performance Measure (NPM) framework
will be implemented with states
selecting 8 of 15 NPMs for their
programmatic focus; (3) State-level data
for the selected NPMs will be provided
by MCHB from national data sources
thus reducing burden; (4) For each
selected NPM, the state will establish
and report only on a Structural/Process
Measure (S&PM); (5) Revised
instructions for the State Application/
Annual Report process reflect the need
for state priority needs and national
MCH priority areas to drive the state’s
reporting on the 5-year (and ongoing)
Needs Assessment findings, the
selection of NPMs which target the
state-identified priority needs, the
development of evidence-based
strategies and S&PMs for addressing the
selected NPMs, and the establishment of
State Performance Measures which
respond to the state’s identified unique
needs; (6) State Application/Annual
Report will include a 5-year Action Plan
for addressing the identified MCH
priority areas; (7) An Executive
Summary will be included with each
submitted Application/Annual Report;
(8) A 5-year Needs Assessment
Summary will be integrated into the
State’s Application/Annual Report and
will replace the more comprehensive,
Number of
respondents
Form name
Application and Annual Report without 5-Year Needs Assessment ..........................................................................
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15:30 Jun 26, 2014
Jkt 232001
PO 00000
Frm 00083
Number of
responses per
respondent
59
Fmt 4703
Sfmt 4703
standalone 5-year Needs Assessment
document that the state previously
submitted; (9) Health System Capacity
Indicators will be eliminated; (10) Data
for Health Status Indicators will be
provided by the MCHB, as available,
rather than collected and reported by
the state; and (11) Federal and State
Title V Program budget and
expenditures will be reported separately
by the state.
Need and Proposed Use of the
Information: Each year, all states and
jurisdictions are required to submit an
Application/Annual Report for federal
funds for their Title V MCH Services
Block Grant to States Program to
HRSA’s MCHB (Section 505(a) of Title
V of the Social Security Act). In
addition, the state/jurisdictional MCH
Block Grant programs are required to
conduct a statewide, comprehensive
Needs Assessment every 5 years. The
information and instructions for the
preparation and submission of this
Application/Annual Report are
contained in the Title V Maternal and
Child Health Services Block Grant to
States Program: Guidance and Forms for
the Title V Application/Annual Report.
Likely Respondents: By legislation
(Section 505(a) of Title V of the Social
Security Act), the MCH Block Grant
Application/Annual Report must be
developed by, or in consultation with,
the State MCH Health agency.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install and utilize
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this Information
Collection Request are summarized in
the table below.
Total Estimated Annualized burden
hours:
Total
responses
1
E:\FR\FM\27JNN1.SGM
59
27JNN1
Burden per
response
(in hours)
123.0
Total burden
hours
7,257
Federal Register / Vol. 79, No. 124 / Friday, June 27, 2014 / Notices
Number of
respondents
Form name
Application and Annual Report with 5-Year Needs Assessment ..................................................................................
Average Total Annual Burden .............................................
59
59
Number of
responses per
respondent
Total
responses
1
........................
59
59
Burden per
response
(in hours)
189.3
........................
36539
Total burden
hours
11,169
* 8,561
* (Reflects the average of one Application/Annual Report with Needs Assessment and two Application/Annual Reports without Needs
Assessment.)
In fiscal year (FY) 2016, states and
jurisdictions will be submitting an
application and annual report with a 5year needs assessment for a total
estimated burden of 11,169 hours. In FY
2017 and FY 2018, states and
jurisdictions will be submitting an
application and annual report without a
5-year needs assessment for a total
estimated burden of 14,514.
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Dated: June 20, 2014.
Jackie Painter,
Acting Director, Division of Policy and
Information Coordination.
[FR Doc. 2014–15051 Filed 6–26–14; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
National Vaccine Injury Compensation
Program; List of Petitions Received
Health Resources and Services
Administration, HHS.
ACTION: Notice.
AGENCY:
The Health Resources and
Services Administration (HRSA) is
publishing this notice of petitions
received under the National Vaccine
Injury Compensation Program (the
Program), as required by Section
2112(b)(2) of the Public Health Service
(PHS) Act, as amended. While the
Secretary of Health and Human Services
is named as the respondent in all
proceedings brought by the filing of
petitions for compensation under the
Program, the United States Court of
Federal Claims is charged by statute
with responsibility for considering and
acting upon the petitions.
wreier-aviles on DSK5TPTVN1PROD with NOTICES
SUMMARY:
VerDate Mar<15>2010
15:30 Jun 26, 2014
Jkt 232001
For
information about requirements for
filing petitions, and the Program in
general, contact the Clerk, United States
Court of Federal Claims, 717 Madison
Place NW., Washington, DC 20005,
(202) 357–6400. For information on
HRSA’s role in the Program, contact the
Director, National Vaccine Injury
Compensation Program, 5600 Fishers
Lane, Room 11C–26, Rockville, MD
20857; (301) 443–6593.
SUPPLEMENTARY INFORMATION: The
Program provides a system of no-fault
compensation for certain individuals
who have been injured by specified
childhood vaccines. Subtitle 2 of Title
XXI of the PHS Act, 42 U.S.C. 300aa–
10 et seq., provides that those seeking
compensation are to file a petition with
the U.S. Court of Federal Claims and to
serve a copy of the petition on the
Secretary of Health and Human
Services, who is named as the
respondent in each proceeding. The
Secretary has delegated this
responsibility under the Program to
HRSA. The Court is directed by statute
to appoint special masters who take
evidence, conduct hearings as
appropriate, and make initial decisions
as to eligibility for, and amount of,
compensation.
A petition may be filed with respect
to injuries, disabilities, illnesses,
conditions, and deaths resulting from
vaccines described in the Vaccine Injury
Table (the Table) set forth at Section
2114 of the PHS Act or as set forth at
42 CFR 100.3, as applicable. This Table
lists for each covered childhood vaccine
the conditions which may lead to
compensation and, for each condition,
the time period for occurrence of the
first symptom or manifestation of onset
or of significant aggravation after
vaccine administration. Compensation
may also be awarded for conditions not
listed in the Table and for conditions
that are manifested outside the time
periods specified in the Table, but only
if the petitioner shows that the
condition was caused by one of the
listed vaccines.
Section 2112(b)(2) of the PHS Act, 42
U.S.C. 300aa–12(b)(2), requires that
‘‘[w]ithin 30 days after the Secretary
receives service of any petition filed
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00084
Fmt 4703
Sfmt 4703
under section 2111 the Secretary shall
publish notice of such petition in the
Federal Register.’’ Set forth below is a
list of petitions received by HRSA on
May 1, 2014, through May 31, 2014.
This list provides the name of
petitioner, city and state of vaccination
(if unknown then city and state of
person or attorney filing claim), and
case number. In cases where the Court
has redacted the name of a petitioner
and/or the case number, the list reflects
such redaction.
Section 2112(b)(2) also provides that
the special master ‘‘shall afford all
interested persons an opportunity to
submit relevant, written information’’
relating to the following:
1. The existence of evidence ‘‘that
there is not a preponderance of the
evidence that the illness, disability,
injury, condition, or death described in
the petition is due to factors unrelated
to the administration of the vaccine
described in the petition,’’ and
2. Any allegation in a petition that the
petitioner either:
(a) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition not set forth in the
Vaccine Injury Table but which was
caused by’’ one of the vaccines referred
to in the Table, or
(b) ‘‘Sustained, or had significantly
aggravated, any illness, disability,
injury, or condition set forth in the
Vaccine Injury Table the first symptom
or manifestation of the onset or
significant aggravation of which did not
occur within the time period set forth in
the Table but which was caused by a
vaccine’’ referred to in the Table.
In accordance with Section
2112(b)(2), all interested persons may
submit written information relevant to
the issues described above in the case of
the petitions listed below. Any person
choosing to do so should file an original
and three (3) copies of the information
with the Clerk of the U.S. Court of
Federal Claims at the address listed
above (under the heading FOR FURTHER
INFORMATION CONTACT), with a copy to
HRSA addressed to Director, Division of
Vaccine Injury Compensation Program,
Healthcare Systems Bureau, 5600
Fishers Lane, Room 11C–26, Rockville,
MD 20857. The Court’s caption
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]]>Agencies
[Federal Register Volume 79, Number 124 (Friday, June 27, 2014)]
[Notices]
[Pages 36537-36539]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-15051]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request
AGENCY: Health Resources and Services Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects (Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995), the Health Resources and Services
Administration (HRSA) announces plans to submit an Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). Prior to submitting the ICR to OMB, HRSA seeks
comments from the public regarding the burden estimate, below, or any
other aspect of the ICR.
DATES: Comments on this Information Collection Request must be received
no later than August 26, 2014.
[[Page 36538]]
ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance Officer, Room 10-29, Parklawn
Building, 5600 Fishers Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email paperwork@hrsa.gov or call the HRSA
Information Collection Clearance Officer at (301) 443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information request collection title
for reference.
Information Collection Request Title: Title V Maternal and Child
Health Services Block Grant to States Program: Guidance and Forms for
the Title V Application/Annual Report OMB No. 0915-0172--Revision.
Abstract: HRSA is revising the Title V Maternal and Child Health
Services Block Grant to States Program: Guidance and Forms for the
Title V Application/Annual Report. The Guidance is used annually by the
50 states and nine jurisdictions in applying for Block Grants under
Title V of the Social Security Act and in preparing the required Annual
Report. In partnership with the leadership in State Title V Maternal
and Child Health (MCH) programs as well as with other national MCH
leaders and stakeholders, HRSA's Maternal and Child Health Bureau
(MCHB) has been working over the past year to develop and refine a
vision for transforming the MCH Block Grant to States Program to better
meet current and future challenges facing our nation's mothers and
children, including children with special health care needs (CSHCN) and
their families. The proposed revisions to the Application and Annual
Reporting requirements and to the data forms that are contained in the
revised Guidance reflect this vision.
The aims of the MCH Block Grant to States Program transformation
are threefold: (1) Reduce burden to states, (2) maintain state
flexibility, and (3) improve accountability. Revisions to this edition
are intended to enable the state to tell a more cohesive and
comprehensive Title V story and to better reflect on the program's
leadership role and its contributions to the state's public health
system in building improved and expanded systems of care for the MCH
population. It is recognized that the full extent of the anticipated
burden reduction will be realized over time as states become more
familiar with the new instructions and reporting requirements. The
burden estimates presented in the table below are based on previous
burden estimates and consultations with a few states on the proposed
changes. HRSA plans to solicit additional information from no more than
nine states to derive more accurate estimates.
Specific changes to this edition of the Title V Maternal and Child
Health Services Block Grant to States Program: Guidance and Forms for
the Title V Application/Annual Report include the following:
(1) Narrative reporting will be organized by six population health
domains (i.e., maternal and women's health, perinatal health, child
health, CSHCN, adolescent health, and life course); (2) Revised
National Performance Measure (NPM) framework will be implemented with
states selecting 8 of 15 NPMs for their programmatic focus; (3) State-
level data for the selected NPMs will be provided by MCHB from national
data sources thus reducing burden; (4) For each selected NPM, the state
will establish and report only on a Structural/Process Measure (S&PM);
(5) Revised instructions for the State Application/Annual Report
process reflect the need for state priority needs and national MCH
priority areas to drive the state's reporting on the 5-year (and
ongoing) Needs Assessment findings, the selection of NPMs which target
the state-identified priority needs, the development of evidence-based
strategies and S&PMs for addressing the selected NPMs, and the
establishment of State Performance Measures which respond to the
state's identified unique needs; (6) State Application/Annual Report
will include a 5-year Action Plan for addressing the identified MCH
priority areas; (7) An Executive Summary will be included with each
submitted Application/Annual Report; (8) A 5-year Needs Assessment
Summary will be integrated into the State's Application/Annual Report
and will replace the more comprehensive, standalone 5-year Needs
Assessment document that the state previously submitted; (9) Health
System Capacity Indicators will be eliminated; (10) Data for Health
Status Indicators will be provided by the MCHB, as available, rather
than collected and reported by the state; and (11) Federal and State
Title V Program budget and expenditures will be reported separately by
the state.
Need and Proposed Use of the Information: Each year, all states and
jurisdictions are required to submit an Application/Annual Report for
federal funds for their Title V MCH Services Block Grant to States
Program to HRSA's MCHB (Section 505(a) of Title V of the Social
Security Act). In addition, the state/jurisdictional MCH Block Grant
programs are required to conduct a statewide, comprehensive Needs
Assessment every 5 years. The information and instructions for the
preparation and submission of this Application/Annual Report are
contained in the Title V Maternal and Child Health Services Block Grant
to States Program: Guidance and Forms for the Title V Application/
Annual Report.
Likely Respondents: By legislation (Section 505(a) of Title V of
the Social Security Act), the MCH Block Grant Application/Annual Report
must be developed by, or in consultation with, the State MCH Health
agency.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose or provide the
information requested. This includes the time needed to review
instructions; to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information; to train personnel and to be able to respond to
a collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this Information Collection Request are summarized in the table below.
Total Estimated Annualized burden hours:
----------------------------------------------------------------------------------------------------------------
Number of Burden per
Form name Number of responses per Total response (in Total burden
respondents respondent responses hours) hours
----------------------------------------------------------------------------------------------------------------
Application and Annual Report 59 1 59 123.0 7,257
without 5-Year Needs Assessment
[[Page 36539]]
Application and Annual Report 59 1 59 189.3 11,169
with 5-Year Needs Assessment...
Average Total Annual Burden..... 59 .............. 59 .............. * 8,561
----------------------------------------------------------------------------------------------------------------
* (Reflects the average of one Application/Annual Report with Needs Assessment and two Application/Annual
Reports without Needs Assessment.)
In fiscal year (FY) 2016, states and jurisdictions will be
submitting an application and annual report with a 5-year needs
assessment for a total estimated burden of 11,169 hours. In FY 2017 and
FY 2018, states and jurisdictions will be submitting an application and
annual report without a 5-year needs assessment for a total estimated
burden of 14,514.
HRSA specifically requests comments on (1) the necessity and
utility of the proposed information collection for the proper
performance of the agency's functions, (2) the accuracy of the
estimated burden, (3) ways to enhance the quality, utility, and clarity
of the information to be collected, and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
Dated: June 20, 2014.
Jackie Painter,
Acting Director, Division of Policy and Information Coordination.
[FR Doc. 2014-15051 Filed 6-26-14; 8:45 am]
BILLING CODE 4165-15-P
