Foreign-Trade Zone (FTZ) 93-Raleigh/Durham, North Carolina; Authorization of Production Activity; GlaxoSmithKline, PLC (Pharmaceutical Products), Zebulon, North Carolina, 28459 [2019-12990]
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28459
Notices
Federal Register
Vol. 84, No. 118
Wednesday, June 19, 2019
This section of the FEDERAL REGISTER
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DEPARTMENT OF AGRICULTURE
Submission for OMB Review;
Comment Request
jbell on DSK3GLQ082PROD with NOTICES
June 13, 2019.
The Department of Agriculture has
submitted the following information
collection requirement(s) to OMB for
review and clearance under the
Paperwork Reduction Act of 1995,
Public Law 104–13. Comments are
requested regarding: Whether the
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility; the accuracy of the
agency’s estimate of burden including
the validity of the methodology and
assumptions used; ways to enhance the
quality, utility and clarity of the
information to be collected; and ways to
minimize the burden of the collection of
information on those who are to
respond, including through the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Comments regarding this information
collection received by July 18, 2019 will
be considered. Written comments
should be addressed to: Desk Officer for
Agriculture, Office of Information and
Regulatory Affairs, Office of
Management and Budget (OMB), New
Executive Office Building, 725 17th
Street NW, Washington, DC 20502.
Commenters are encouraged to submit
their comments to OMB via email to:
OIRA_Submission@OMB.EOP.GOV or
fax (202) 395–5806 and to Departmental
Clearance Office, USDA, OCIO, Mail
Stop 7602, Washington, DC 20250–
7602. Copies of the submission(s) may
be obtained by calling (202) 720–8958.
An agency may not conduct or
sponsor a collection of information
unless the collection of information
displays a currently valid OMB control
number and the agency informs
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potential persons who are to respond to
the collection of information that such
persons are not required to respond to
the collection of information unless it
displays a currently valid OMB control
number.
National Institute of Food and
Agriculture
Title: Reporting Requirements for
State Plans of Work for Agricultural
Research and Extension Formula Funds.
OMB Control Number: 0524–0036.
Summary of Collection: Section 202
and 225 of the Agricultural Research,
Extension, and Education Reform Act of
1998 (AREERA) which requires that a
plan of work must be submitted by each
institution and approved by the
National Institute of Food and
Agriculture (NIFA) before formula funds
may be provided to the 1862 and 1890
land-grant institutions. The plan of
work must address critical agricultural
issues in the State and describe the
programs and project targeted to address
these issues using the NIFA formula
funds. The plan of work also must
describe the institution’s multistate
activities as well as their integrated
research and extension activities. NIFA
is requesting to continue to collect an
update to the 5-Year Plan of Work
which began with the Fiscal Year 2007,
and as a result no longer needs to collect
the initial 5-Year Plan. Also, as required
by the Food Conservation and Energy
Act of 2008 (FCEA) (Pub. L. 110–246,
Sec. 7505), NIFA is working with the
university partners in extension and
research to review and identify
measures to streamline the submission,
reporting under, and implementation of
plan of work requirements.
Need and Use of the Information:
Institutions are required to annually
report to NIFA the following: (1) The
actions taken to seek stakeholder input
to encourage their participation; (2) a
brief statement of the process used by
the recipient institution to identify
individuals or groups who are
stakeholders and to collect input from
them; and (3) a statement of how
collected input was considered. NIFA
uses the information to provide
feedback to the institutions on their
Plans of Work and Annual Reports of
Accomplishments and Results in order
for institutions to improve the conduct
and the delivery of their programs.
Failure to comply with the
requirements may result in the
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withholding of a recipient institution’s
formula funds and redistribution of its
share of formula funds to other eligible
institutions.
Description of Respondents: Not-forprofit institutions; State, Local or Tribal
Government.
Number of Respondents: 152.
Frequency of Responses: Reporting:
Annually.
Total Burden Hours: 49,248.
Ruth Brown,
Departmental Information Collection
Clearance Officer.
[FR Doc. 2019–12904 Filed 6–18–19; 8:45 am]
BILLING CODE 3410–09–P
DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B–05–2019]
Foreign-Trade Zone (FTZ) 93—Raleigh/
Durham, North Carolina; Authorization
of Production Activity;
GlaxoSmithKline, PLC (Pharmaceutical
Products), Zebulon, North Carolina
On February 13, 2019,
GlaxoSmithKline, PLC, submitted a
notification of proposed production
activity to the FTZ Board for its facility
within FTZ 93, in Zebulon, North
Carolina.
The notification was processed in
accordance with the regulations of the
FTZ Board (15 CFR part 400), including
notice in the Federal Register inviting
public comment (84 FR 6128, February
26, 2019). On June 13, 2019, the
applicant was notified of the FTZ
Board’s decision that no further review
of the activity is warranted at this time.
The production activity described in the
notification was authorized, subject to
the FTZ Act and the FTZ Board’s
regulations, including Section 400.14.
Dated: June 13, 2019.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2019–12990 Filed 6–18–19; 8:45 am]
BILLING CODE 3510–DS–P
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[Federal Register Volume 84, Number 118 (Wednesday, June 19, 2019)]
[Notices]
[Page 28459]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-12990]
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DEPARTMENT OF COMMERCE
Foreign-Trade Zones Board
[B-05-2019]
Foreign-Trade Zone (FTZ) 93--Raleigh/Durham, North Carolina;
Authorization of Production Activity; GlaxoSmithKline, PLC
(Pharmaceutical Products), Zebulon, North Carolina
On February 13, 2019, GlaxoSmithKline, PLC, submitted a
notification of proposed production activity to the FTZ Board for its
facility within FTZ 93, in Zebulon, North Carolina.
The notification was processed in accordance with the regulations
of the FTZ Board (15 CFR part 400), including notice in the Federal
Register inviting public comment (84 FR 6128, February 26, 2019). On
June 13, 2019, the applicant was notified of the FTZ Board's decision
that no further review of the activity is warranted at this time. The
production activity described in the notification was authorized,
subject to the FTZ Act and the FTZ Board's regulations, including
Section 400.14.
Dated: June 13, 2019.
Andrew McGilvray,
Executive Secretary.
[FR Doc. 2019-12990 Filed 6-18-19; 8:45 am]
BILLING CODE 3510-DS-P
