Agency Information Collection Activities; Proposed Collection; Public Comment Request; Annual Reporting Requirements for the Older Americans Act Title VI Grant Program, 9341-9342 [2019-04734]
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Federal Register / Vol. 84, No. 50 / Thursday, March 14, 2019 / Notices
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than April 10, 2019.
A. Federal Reserve Bank of Atlanta
(Kathryn Haney, Assistant Vice
President) 1000 Peachtree Street NE,
Atlanta, Georgia 30309. Comments can
also be sent electronically to
Applications.Comments@atl.frb.org:
1. Community Bancshares of
Mississippi, Inc. Employee Stock
Ownership Plan, Brandon, Mississippi,
to acquire additional voting shares, for
a total of 18.82 percent, of Community
Bancshares of Mississippi, Inc.,
Brandon, Mississippi, and thereby
indirectly acquire shares of Community
Bank of Mississippi, Forest, Mississippi.
Board of Governors of the Federal Reserve
System, March 8, 2019.
Yao-Chin Chao,
Assistant Secretary of the Board.
[FR Doc. 2019–04668 Filed 3–13–19; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
[OMB No. 0985–0007]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request; Annual Reporting
Requirements for the Older Americans
Act Title VI Grant Program
Administration for Community
Living, HHS.
ACTION: Notice
AGENCY:
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17:22 Mar 13, 2019
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The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
comment on the proposed collection of
information listed above. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal agencies are required to
publish a notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice.
This Extension without Change (ICR
Ext) solicits comments on the
information collection requirements
related to the Program Performance
Reports for Title VI grants under the
Older Americans Act.
DATES: Comments on the collection of
information must be submitted
electronically by 11:59 p.m. (EST) or
postmarked by May 13, 2019.
ADDRESSES: Submit electronic
comments on the collection of
information to: Cynthia LaCounte,
Cynthia.LaCounte@acl.hhs.gov. Submit
written comments on the collection of
information to Administration for
Community Living, Washington, DC
20201, Attention: Cynthia LaCounte.
FOR FURTHER INFORMATION CONTACT:
Cynthia LaCounte, Director, Office of
American Indian, Alaskan Native and
Native Hawaiian Programs,
Administration for Community Living,
Washington, DC 20416, 202–795–7380,
Cynthia.LaCounte@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA (44
U.S.C. 3506(c)(2)(A)) requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, ACL is publishing a notice
of the proposed collection of
information set forth in this document.
SUMMARY:
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9341
With respect to the following
collection of information, ACL invites
comments on our burden estimates or
any other aspect of this collection of
information, including:
(1) Whether the proposed collection
of information is necessary for the
proper performance of ACL’s functions,
including whether the information will
have practical utility;
(2) the accuracy of ACL’s estimate of
the burden of the proposed collection of
information, including the validity of
the methodology and assumptions used
to determine burden estimates;
(3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) ways to minimize the burden of
the collection of information on
respondents, including through the use
of automated collection techniques
when appropriate, and other forms of
information technology.
The purpose of the Program
Performance Report data collection
provides a data base for ACL to: (1)
Monitor program achievement of
performance objective; (2) establish
program policy and direction; and (3)
prepare responses to Congress, the
OMB, the General Accounting Office,
other Federal Departments, and public
and private agencies as required by the
OAA Title II sections 202(f)(1) and 207.
This data collection will also support
ACL in tracking performance outcomes
and efficiency measures with respect to
the annual and long-term performance
targets established in compliance with
the Government Performance Results
Modernization Act (GPRAMA). If ACL
did not collect the program data herein
requested, it would not be able to
monitor and manage total program
progress as expected, nor develop
program policy options directed toward
assuring the most effective use of
limited Title VI funds.
The proposed data collection tools
may be found on the ACL website for
review at https://www.acl.gov/aboutacl/public-input.
Estimated Program Burden
ACL estimates the burden associated
with this collection of information as
follows: 274 tribal grantees respond
annually and it will take 2.5 hours to
complete the Title VI report for each
grantee for a total of 685 hours for all
tribal grantees to complete the form.
E:\FR\FM\14MRN1.SGM
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9342
Federal Register / Vol. 84, No. 50 / Thursday, March 14, 2019 / Notices
Number of
respondents
Respondent/data collection activity
Responses
per
respondent
Hours per
response
Annual burden
hours
Title VI Part A, B and C ...................................................................................
274
1
2.5
685
Total ..........................................................................................................
274
1
2.5
685
Dated: March 5, 2019.
Mary Lazare,
Principal Deputy Administrator.
[FR Doc. 2019–04734 Filed 3–13–19; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–N–4002]
Electronic Submission of Adverse
Event Reports to the Food and Drug
Administration Adverse Event
Reporting System Using International
Council for Harmonisation E2B(R3)
Standards; Public Meetings; Request
for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public meetings;
request for comments.
ACTION:
The Food and Drug
Administration (FDA, the Agency, or
we) is re-announcing three public
meetings entitled ‘‘Electronic
Submission of Adverse Event Reports to
FDA Adverse Event Reporting System
(FAERS) Using International Council for
Harmonisation (ICH) E2B(R3)
Standards.’’ The purpose of these public
meetings is to provide the
pharmaceutical industry and other
interested parties with information on
the plans, progress, and technical
specifications to upgrade electronic
submission standards for drug,
biological, and drug/biologic-led
combination products for the premarket
and postmarket safety surveillance
programs managed by the Center for
Drug Evaluation and Research (CDER)
and the Center for Biologics Evaluation
and Research (CBER). These meetings
will focus on enhancements to
electronic submission of Individual
Case Safety Reports (ICSRs) in FAERS
using ICH E2B(R3) standards.
FDA is seeking input from
stakeholders as it fulfills its
commitment to implement ICH E2B(R3)
standards by holding three public
meetings. FDA will use the information
provided by the public to inform the
enhancements to FAERS required for
the implementation of ICH E2B(R3)
SUMMARY:
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standards and relevant regional
variations.
DATES: The first public meeting is being
rescheduled due to a previous lapse in
appropriations. The rescheduled first
public meeting will be held on March
25, 2019, from 9 a.m. to 4 p.m. The
second public meeting will be held on
July 17, 2019, from 9 a.m. to 4 p.m. The
third public meeting will be held on
February 19, 2020, from 9 a.m. to 4 p.m.
Submit either electronic or written
comments on these public meetings by
April 25, 2019, for the first public
meeting; by August 16, 2019, for the
second public meeting, and by March
20, 2020, for the third public meeting.
See the SUPPLEMENTARY INFORMATION
section for registration dates and
information.
The first public meeting
will be held at the Silver Spring Civic
Building at Veterans Plaza, The Buffalo
Soldiers Great Hall, 1 Veterans Pl.,
Silver Spring, MD 20910. The second
and third public meetings will be held
at the FDA White Oak Campus, 10903
New Hampshire Ave., Bldg. 31
Conference Center, the Great Room (Rm.
1503, Section A), Silver Spring, MD
20993–0002. Entrance for the public
meeting participants (non-FDA
employees) is through Building 1, where
routine security check procedures will
be performed. For parking and security
information, please refer to https://
www.fda.gov/AboutFDA/
WorkingatFDA/BuildingsandFacilities/
WhiteOakCampusInformation/
default.htm.
You may submit comments as
follows. Please note that late, untimely
filed comments will not be considered.
For timely consideration, we request
that electronic comments be submitted
before or within 30 days after each
public meeting (i.e., comments
submitted by or before April 25, 2019,
for the first public meeting; August 16,
2019, for the second public meeting;
and March 20, 2020, for the third public
meeting. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
April 25, 2019, August 16, 2019, and
March 20, 2020, after the first, second,
and the third meeting, respectively.
Comments received by mail/hand
ADDRESSES:
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delivery/courier (for written/paper
submissions) will be considered timely
if they are postmarked or the delivery
service acceptance receipt is on or
before that date.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2018–N–4002 for ‘‘Electronic
Submission of Adverse Event Reports to
FAERS Using ICH E2B(R3) Standards.’’
Received comments, those filed in a
timely manner (see ADDRESSES), will be
E:\FR\FM\14MRN1.SGM
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]]>Agencies
[Federal Register Volume 84, Number 50 (Thursday, March 14, 2019)]
[Notices]
[Pages 9341-9342]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-04734]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
[OMB No. 0985-0007]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request; Annual Reporting Requirements for the Older
Americans Act Title VI Grant Program
AGENCY: Administration for Community Living, HHS.
ACTION: Notice
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing an
opportunity for the public to comment on the proposed collection of
information listed above. Under the Paperwork Reduction Act of 1995
(the PRA), Federal agencies are required to publish a notice in the
Federal Register concerning each proposed collection of information,
including each proposed extension of an existing collection of
information, and to allow 60 days for public comment in response to the
notice.
This Extension without Change (ICR Ext) solicits comments on the
information collection requirements related to the Program Performance
Reports for Title VI grants under the Older Americans Act.
DATES: Comments on the collection of information must be submitted
electronically by 11:59 p.m. (EST) or postmarked by May 13, 2019.
ADDRESSES: Submit electronic comments on the collection of information
to: Cynthia LaCounte, Cynthia.LaCounte@acl.hhs.gov. Submit written
comments on the collection of information to Administration for
Community Living, Washington, DC 20201, Attention: Cynthia LaCounte.
FOR FURTHER INFORMATION CONTACT: Cynthia LaCounte, Director, Office of
American Indian, Alaskan Native and Native Hawaiian Programs,
Administration for Community Living, Washington, DC 20416, 202-795-
7380, Cynthia.LaCounte@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party.
Section 3506(c)(2)(A) of the PRA (44 U.S.C. 3506(c)(2)(A)) requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each
proposed extension of an existing collection of information, before
submitting the collection to OMB for approval. To comply with this
requirement, ACL is publishing a notice of the proposed collection of
information set forth in this document.
With respect to the following collection of information, ACL
invites comments on our burden estimates or any other aspect of this
collection of information, including:
(1) Whether the proposed collection of information is necessary for
the proper performance of ACL's functions, including whether the
information will have practical utility;
(2) the accuracy of ACL's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used to determine burden estimates;
(3) ways to enhance the quality, utility, and clarity of the
information to be collected; and
(4) ways to minimize the burden of the collection of information on
respondents, including through the use of automated collection
techniques when appropriate, and other forms of information technology.
The purpose of the Program Performance Report data collection
provides a data base for ACL to: (1) Monitor program achievement of
performance objective; (2) establish program policy and direction; and
(3) prepare responses to Congress, the OMB, the General Accounting
Office, other Federal Departments, and public and private agencies as
required by the OAA Title II sections 202(f)(1) and 207. This data
collection will also support ACL in tracking performance outcomes and
efficiency measures with respect to the annual and long-term
performance targets established in compliance with the Government
Performance Results Modernization Act (GPRAMA). If ACL did not collect
the program data herein requested, it would not be able to monitor and
manage total program progress as expected, nor develop program policy
options directed toward assuring the most effective use of limited
Title VI funds.
The proposed data collection tools may be found on the ACL website
for review at https://www.acl.gov/about-acl/public-input.
Estimated Program Burden
ACL estimates the burden associated with this collection of
information as follows: 274 tribal grantees respond annually and it
will take 2.5 hours to complete the Title VI report for each grantee
for a total of 685 hours for all tribal grantees to complete the form.
[[Page 9342]]
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Annual burden
Respondent/data collection activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Title VI Part A, B and C........................ 274 1 2.5 685
rrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrr
Total....................................... 274 1 2.5 685
----------------------------------------------------------------------------------------------------------------
Dated: March 5, 2019.
Mary Lazare,
Principal Deputy Administrator.
[FR Doc. 2019-04734 Filed 3-13-19; 8:45 am]
BILLING CODE 4154-01-P
