Meetings To Implement Pandemic Response Voluntary Agreement Under Section 708 of the Defense Production Act, 53974-53975 [2021-21192]
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53974
Federal Register / Vol. 86, No. 186 / Wednesday, September 29, 2021 / Notices
matters relating to national maritime
security.
Agenda
(1) Call to Order.
(2) Introduction.
(3) Designated Federal Official Remarks.
(4) Roll call of Committee members and
determination of quorum.
(5) Remarks from U.S. Coast Guard
Senior Leadership.
(6) Swearing in of Committee Members.
(7) Election by Committee members of
Chair and Vice-Chair.
(8) Presentation of tasks. The Coast
Guard will present the following
tasks and the Committee will
determine if they will accept the
tasks and form working groups:
a. Provide feedback on cyber
vulnerability assessments that are
being conducted within the
industry.
b. Provide input to support further
development of the Maritime Cyber
Risk Assessment Model.
(9) Public comment period.
(10) Closing Remarks/plans for next
meeting.
(11) Adjournment of meeting.
A copy of all meeting documentation
will be available at https://homeport.
uscg.mil/NMSAC by October 15, 2021.
Alternatively, you may contact Mr. Ryan
Owens as noted in the FOR FURTHER
INFORMATION section above. There will
be a public comment period at the end
of the meeting. Speakers are requested
to limit their comments to 3 minutes.
Please note that the public comment
period may end before the period
allotted, following the last call for
comments. Contact the individual listed
in the FOR FURTHER INFORMATION
CONTACT section above to register as a
speaker.
Dated: September 23, 2021.
Wayne R. Arguin, Jr.,
Captain, U.S. Coast Guard, Director of
Inspections and Compliance.
[FR Doc. 2021–21159 Filed 9–28–21; 8:45 am]
BILLING CODE 9110–04–P
The date of revocation is
September 29, 2021.
DATES:
Dr.
Eugene Bondoc, Laboratories and
Scientific Services Directorate, U.S.
Customs and Border Protection, 1300
Pennsylvania Avenue NW, Suite 1500N,
Washington, DC 20229, tel. 202–344–
1060.
FOR FURTHER INFORMATION CONTACT:
Notice is
hereby given that, regarding Trust
Control International (Trust Control),
2800 Post Oak Blvd., Suite 4100,
Williams Tower, Houston, TX 77056,
Trust Control’s approval has been
indefinitely revoked from gauging
petroleum and petroleum products for
customs purposes in accordance with
section 151.13 of the U.S. Customs and
Border Protection (CBP) regulations in
title 19 of the Code of Federal
Regulations (CFR), (19 CFR 151.13). The
basis for this revocation is pursuant to
19 CFR 151.13(d)(1)(vii), for the failure
to meet the obligation as a CBPapproved commercial gauger to
maintain a customs bond in accordance
with part 113 of the CBP regulations (19
CFR part 113).
Inquiries regarding the entity’s status
as an approved gauger may be directed
to CBP by calling (202) 344–1060 or by
sending an email to CBPGaugersLabs@
cbp.dhs.gov. Please reference the
website listed below for a complete
listing of CBP-approved commercial
gaugers and accredited laboratories.
https://www.cbp.gov/about/labsscientific/commercial-gaugers-andlaboratories
SUPPLEMENTARY INFORMATION:
Dated: September 23, 2021.
Larry D. Fluty,
Executive Director, Laboratories and
Scientific Services.
DEPARTMENT OF HOMELAND
SECURITY
U.S. Customs and Border Protection
[FR Doc. 2021–21088 Filed 9–28–21; 8:45 am]
BILLING CODE 9111–14–P
Revocation of Trust Control
International (Houston, TX), as an
Approved Commercial Gauger
lotter on DSK11XQN23PROD with NOTICES1
Notice is hereby given,
pursuant to the U.S. Customs and
Border Protection (CBP) regulations,
that CBP’s approval for Trust Control
International’s Houston, Texas, facility
has been revoked from gauging
petroleum and petroleum products for
customs purposes.
SUMMARY:
U.S. Customs and Border
Protection, Department of Homeland
Security.
ACTION: General notice of revocation of
Trust Control International as a
customs-approved gauger.
AGENCY:
VerDate Sep<11>2014
18:22 Sep 28, 2021
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DEPARTMENT OF HOMELAND
SECURITY
Federal Emergency Management
Agency
[Docket ID FEMA–2020–0016]
Meetings To Implement Pandemic
Response Voluntary Agreement Under
Section 708 of the Defense Production
Act
Federal Emergency
Management Agency, Department of
Homeland Security.
ACTION: Announcement of meetings.
AGENCY:
The Federal Emergency
Management Agency (FEMA) held two
meetings to implement the Voluntary
Agreement for the Manufacture and
Distribution of Critical Healthcare
Resources Necessary to Respond to a
Pandemic.
DATES: The first meeting took place on
Tuesday, September 21, 2021, from 10
a.m. to 12 p.m. Eastern Time (ET). The
second meeting took place on Thursday,
September 23, 2021, from 10 a.m. to 12
p.m. ET.
FOR FURTHER INFORMATION CONTACT:
Robert Glenn, Office of Business,
Industry, Infrastructure Integration, via
email at OB3I@fema.dhs.gov or via
phone at (202) 212–1666.
SUPPLEMENTARY INFORMATION: Notice of
these meetings is provided as required
by section 708(h)(8) of the Defense
Production Act (DPA), 50 U.S.C.
4558(h)(8), and consistent with 44 CFR
part 332.
The DPA authorizes the making of
‘‘voluntary agreements and plans of
action’’ with representatives of industry,
business, and other interests to help
provide for the national defense.1 The
President’s authority to facilitate
voluntary agreements with respect to
responding to the spread of COVID–19
within the United States was delegated
to the Secretary of Homeland Security
in Executive Order 13911.2 The
Secretary of Homeland Security further
delegated this authority to the FEMA
Administrator.3
On August 17, 2020, after the
appropriate consultations with the
Attorney General and the Chairman of
the Federal Trade Commission, FEMA
completed and published in the Federal
Register a ‘‘Voluntary Agreement,
Manufacture and Distribution of Critical
Healthcare Resources Necessary to
SUMMARY:
1 50
U.S.C. 4558(c)(1).
FR 18403 (Apr. 1, 2020).
3 DHS Delegation 09052, Rev. 00.1 (Apr. 1, 2020);
DHS Delegation Number 09052 Rev. 00 (Jan. 3,
2017).
2 85
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Federal Register / Vol. 86, No. 186 / Wednesday, September 29, 2021 / Notices
lotter on DSK11XQN23PROD with NOTICES1
Respond to a Pandemic’’ (Voluntary
Agreement).4 Unless terminated earlier,
the Voluntary Agreement is effective
until August 17, 2025, and may be
extended subject to additional approval
by the Attorney General after
consultation with the Chairman of the
Federal Trade Commission. The
Agreement may be used to prepare for
or respond to any pandemic, including
COVID–19, during that time.
On December 7, 2020, the first plan of
action under the Voluntary
Agreement—the Plan of Action to
Establish a National Strategy for the
Manufacture, Allocation, and
Distribution of Personal Protective
Equipment (PPE) to Respond to COVID–
19 (PPE Plan of Action)—was finalized.5
The PPE Plan of Action established
several sub-committees under the
Voluntary Agreement, focusing on
different aspects of the PPE Plan of
Action.
On May 24, 2021, four additional
plans of action under the Voluntary
Agreement—the Plan of Action to
Establish a National Strategy for the
Manufacture, Allocation, and
Distribution of Diagnostic Test Kits and
other Testing Components to respond to
COVID–19, the Plan of Action to
Establish a National Strategy for the
Manufacture, Allocation, and
Distribution of Drug Products, Drug
Substances, and Associated Medical
Devices to respond to COVID–19, the
Plan of Action to Establish a National
Strategy for the Manufacture,
Allocation, and Distribution of Medical
Devices to respond to COVID–19, and
the Plan of Action to Establish a
National Strategy for the Manufacture,
Allocation, and Distribution of Medical
Gases to respond to COVID–19—were
finalized.6 These plans of action
established several sub-committees
under the Voluntary Agreement,
focusing on different aspects of each
plan of action.
The meetings were chaired by the
FEMA Administrator or her delegate
and attended by the Attorney General
and the Chairman of the Federal Trade
Commission or their delegates. In
implementing the Voluntary Agreement,
FEMA adheres to all procedural
4 85 FR 50035 (Aug. 17, 2020). The Attorney
General, in consultation with the Chairman of the
Federal Trade Commission, made the required
finding that the purpose of the voluntary agreement
may not reasonably be achieved through an
agreement having less anticompetitive effects or
without any voluntary agreement and published the
finding in the Federal Register on the same day. 85
FR 50049 (Aug. 17, 2020).
5 See 85 FR 78869 (Dec. 7, 2020). See also 85 FR
79020 (Dec. 8, 2020).
6 See 86 FR 27894 (May 24, 2021). See also 86 FR
28851 (May 28, 2021).
VerDate Sep<11>2014
18:22 Sep 28, 2021
Jkt 253001
requirements of 50 U.S.C. 4558 and 44
CFR part 332.
Meeting Objectives: The objectives of
the meetings were as follows:
1. Gather committee Participants and
Attendees to ask targeted questions for
situational awareness related to the
active Plans of Action (PPE, Drug
Products and Drug Substances,
Diagnostic Test Kits, Medical Devices,
and Medical Gases).
2. Establish priorities for COVID–19
response under the Voluntary
Agreement.
3. Identify tasks that should be
completed under the appropriate SubCommittee.
4. Identify information gaps and areas
that merit sharing (both from FEMA to
the private sector and vice versa).
Meetings Closed to the Public: By
default, the DPA requires meetings held
to implement a voluntary agreement or
plan of action be open to the public.7
However, attendance may be limited if
the Sponsor 8 of the voluntary
agreement finds that the matter to be
discussed at a meeting falls within the
purview of matters described in 5 U.S.C.
552b(c), such as trade secrets and
commercial or financial information.
The Sponsor of the Voluntary
Agreement, the FEMA Administrator,
found that these meetings to implement
the Voluntary Agreement involved
matters which fall within the purview of
matters described in 5 U.S.C. 552b(c)
and the meetings were therefore closed
to the public.
Specifically, these meetings to
implement the Voluntary Agreement
may have required participants to
disclose trade secrets or commercial or
financial information that is privileged
or confidential. Disclosure of such
information allows for meetings to be
closed pursuant to 5 U.S.C. 552b(c)(4).
In addition, the success of the Voluntary
Agreement depends wholly on the
willing and enthusiastic participation of
private sector participants. Failure to
close these meetings could have had a
strong chilling effect on private sector
participation and caused a substantial
risk that sensitive information would be
prematurely released to the public,
leading to participants withdrawing
their support from the Voluntary
Agreement.
This would have significantly
frustrated the implementation of the
Voluntary Agreement. Frustration of an
agency’s objective due to premature
7 See
50 U.S.C. 4558(h)(7).
individual designated by the President in
subsection (c)(2) [of section 708 of the DPA] to
administer the voluntary agreement, or plan of
action.’’ 50 U.S.C. 4558(h)(7).
8 ‘‘[T]he
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53975
disclosure of information allows for the
closure of a meeting pursuant to 5
U.S.C. 552b(c)(9)(B).
Deanne Criswell,
Administrator, Federal Emergency
Management Agency.
[FR Doc. 2021–21192 Filed 9–28–21; 8:45 am]
BILLING CODE 9111–19–P
DEPARTMENT OF HOMELAND
SECURITY
Generic Clearance for the Collection of
Qualitative Feedback on Agency
Service Delivery, 1601–0014
Department of Homeland
Security, (DHS).
ACTION: 30-Day notice and request for
comments; extension without change of
a currently approved Collection, 1601–
0014.
AGENCY:
The Department of Homeland
Security, will submit the following
Information Collection Request (ICR) to
the Office of Management and Budget
(OMB) for review and clearance in
accordance with the Paperwork
Reduction Act of 1995. DHS previously
published this information collection
request (ICR) in the Federal Register on
Thursday, May 27, 2021 at for a 60-day
public comment period. There were no
comments received by DHS. The
purpose of this notice is to allow
additional 30-days for public comments.
DATES: Comments are encouraged and
will be accepted until October 29, 2021.
This process is conducted in accordance
with 5 CFR 1320.1.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by electing
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION: Executive
Order 12862 directs Federal agencies to
provide service to the public that
matches or exceeds the best service
available in the private sector. In order
to work continuously to ensure that our
programs are effective and meet our
customers’ needs, Department of
Homeland Security (hereafter ‘‘the
Agency’’) seeks to obtain OMB approval
of a generic clearance to collect
qualitative feedback on our service
delivery. By qualitative feedback we
mean information that provides useful
insights on perceptions and opinions
but are not statistical surveys that yield
SUMMARY:
E:\FR\FM\29SEN1.SGM
29SEN1
Agencies
[Federal Register Volume 86, Number 186 (Wednesday, September 29, 2021)]
[Notices]
[Pages 53974-53975]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-21192]
-----------------------------------------------------------------------
DEPARTMENT OF HOMELAND SECURITY
Federal Emergency Management Agency
[Docket ID FEMA-2020-0016]
Meetings To Implement Pandemic Response Voluntary Agreement Under
Section 708 of the Defense Production Act
AGENCY: Federal Emergency Management Agency, Department of Homeland
Security.
ACTION: Announcement of meetings.
-----------------------------------------------------------------------
SUMMARY: The Federal Emergency Management Agency (FEMA) held two
meetings to implement the Voluntary Agreement for the Manufacture and
Distribution of Critical Healthcare Resources Necessary to Respond to a
Pandemic.
DATES: The first meeting took place on Tuesday, September 21, 2021,
from 10 a.m. to 12 p.m. Eastern Time (ET). The second meeting took
place on Thursday, September 23, 2021, from 10 a.m. to 12 p.m. ET.
FOR FURTHER INFORMATION CONTACT: Robert Glenn, Office of Business,
Industry, Infrastructure Integration, via email at [email protected] or
via phone at (202) 212-1666.
SUPPLEMENTARY INFORMATION: Notice of these meetings is provided as
required by section 708(h)(8) of the Defense Production Act (DPA), 50
U.S.C. 4558(h)(8), and consistent with 44 CFR part 332.
The DPA authorizes the making of ``voluntary agreements and plans
of action'' with representatives of industry, business, and other
interests to help provide for the national defense.\1\ The President's
authority to facilitate voluntary agreements with respect to responding
to the spread of COVID-19 within the United States was delegated to the
Secretary of Homeland Security in Executive Order 13911.\2\ The
Secretary of Homeland Security further delegated this authority to the
FEMA Administrator.\3\
---------------------------------------------------------------------------
\1\ 50 U.S.C. 4558(c)(1).
\2\ 85 FR 18403 (Apr. 1, 2020).
\3\ DHS Delegation 09052, Rev. 00.1 (Apr. 1, 2020); DHS
Delegation Number 09052 Rev. 00 (Jan. 3, 2017).
---------------------------------------------------------------------------
On August 17, 2020, after the appropriate consultations with the
Attorney General and the Chairman of the Federal Trade Commission, FEMA
completed and published in the Federal Register a ``Voluntary
Agreement, Manufacture and Distribution of Critical Healthcare
Resources Necessary to
[[Page 53975]]
Respond to a Pandemic'' (Voluntary Agreement).\4\ Unless terminated
earlier, the Voluntary Agreement is effective until August 17, 2025,
and may be extended subject to additional approval by the Attorney
General after consultation with the Chairman of the Federal Trade
Commission. The Agreement may be used to prepare for or respond to any
pandemic, including COVID-19, during that time.
---------------------------------------------------------------------------
\4\ 85 FR 50035 (Aug. 17, 2020). The Attorney General, in
consultation with the Chairman of the Federal Trade Commission, made
the required finding that the purpose of the voluntary agreement may
not reasonably be achieved through an agreement having less
anticompetitive effects or without any voluntary agreement and
published the finding in the Federal Register on the same day. 85 FR
50049 (Aug. 17, 2020).
---------------------------------------------------------------------------
On December 7, 2020, the first plan of action under the Voluntary
Agreement--the Plan of Action to Establish a National Strategy for the
Manufacture, Allocation, and Distribution of Personal Protective
Equipment (PPE) to Respond to COVID-19 (PPE Plan of Action)--was
finalized.\5\ The PPE Plan of Action established several sub-committees
under the Voluntary Agreement, focusing on different aspects of the PPE
Plan of Action.
---------------------------------------------------------------------------
\5\ See 85 FR 78869 (Dec. 7, 2020). See also 85 FR 79020 (Dec.
8, 2020).
---------------------------------------------------------------------------
On May 24, 2021, four additional plans of action under the
Voluntary Agreement--the Plan of Action to Establish a National
Strategy for the Manufacture, Allocation, and Distribution of
Diagnostic Test Kits and other Testing Components to respond to COVID-
19, the Plan of Action to Establish a National Strategy for the
Manufacture, Allocation, and Distribution of Drug Products, Drug
Substances, and Associated Medical Devices to respond to COVID-19, the
Plan of Action to Establish a National Strategy for the Manufacture,
Allocation, and Distribution of Medical Devices to respond to COVID-19,
and the Plan of Action to Establish a National Strategy for the
Manufacture, Allocation, and Distribution of Medical Gases to respond
to COVID-19--were finalized.\6\ These plans of action established
several sub-committees under the Voluntary Agreement, focusing on
different aspects of each plan of action.
---------------------------------------------------------------------------
\6\ See 86 FR 27894 (May 24, 2021). See also 86 FR 28851 (May
28, 2021).
---------------------------------------------------------------------------
The meetings were chaired by the FEMA Administrator or her delegate
and attended by the Attorney General and the Chairman of the Federal
Trade Commission or their delegates. In implementing the Voluntary
Agreement, FEMA adheres to all procedural requirements of 50 U.S.C.
4558 and 44 CFR part 332.
Meeting Objectives: The objectives of the meetings were as follows:
1. Gather committee Participants and Attendees to ask targeted
questions for situational awareness related to the active Plans of
Action (PPE, Drug Products and Drug Substances, Diagnostic Test Kits,
Medical Devices, and Medical Gases).
2. Establish priorities for COVID-19 response under the Voluntary
Agreement.
3. Identify tasks that should be completed under the appropriate
Sub-Committee.
4. Identify information gaps and areas that merit sharing (both
from FEMA to the private sector and vice versa).
Meetings Closed to the Public: By default, the DPA requires
meetings held to implement a voluntary agreement or plan of action be
open to the public.\7\ However, attendance may be limited if the
Sponsor \8\ of the voluntary agreement finds that the matter to be
discussed at a meeting falls within the purview of matters described in
5 U.S.C. 552b(c), such as trade secrets and commercial or financial
information. The Sponsor of the Voluntary Agreement, the FEMA
Administrator, found that these meetings to implement the Voluntary
Agreement involved matters which fall within the purview of matters
described in 5 U.S.C. 552b(c) and the meetings were therefore closed to
the public.
---------------------------------------------------------------------------
\7\ See 50 U.S.C. 4558(h)(7).
\8\ ``[T]he individual designated by the President in subsection
(c)(2) [of section 708 of the DPA] to administer the voluntary
agreement, or plan of action.'' 50 U.S.C. 4558(h)(7).
---------------------------------------------------------------------------
Specifically, these meetings to implement the Voluntary Agreement
may have required participants to disclose trade secrets or commercial
or financial information that is privileged or confidential. Disclosure
of such information allows for meetings to be closed pursuant to 5
U.S.C. 552b(c)(4). In addition, the success of the Voluntary Agreement
depends wholly on the willing and enthusiastic participation of private
sector participants. Failure to close these meetings could have had a
strong chilling effect on private sector participation and caused a
substantial risk that sensitive information would be prematurely
released to the public, leading to participants withdrawing their
support from the Voluntary Agreement.
This would have significantly frustrated the implementation of the
Voluntary Agreement. Frustration of an agency's objective due to
premature disclosure of information allows for the closure of a meeting
pursuant to 5 U.S.C. 552b(c)(9)(B).
Deanne Criswell,
Administrator, Federal Emergency Management Agency.
[FR Doc. 2021-21192 Filed 9-28-21; 8:45 am]
BILLING CODE 9111-19-P