Proposed Collection; Comment Request, 37240-37241 [2015-16014]
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37240
Federal Register / Vol. 80, No. 125 / Tuesday, June 30, 2015 / Notices
argument that establish that the grant of
the license would not be consistent with
the requirements of 35 U.S.C. 209 and
37 CFR 404.7. Competing applications
completed and received by the U.S.
Army Research Laboratory within
fifteen (15) days from the date of this
published notice will also be treated as
objections to the grant of the
contemplated exclusive license.
Objections submitted in response to
this notice will not be made available to
the public for inspection and, to the
extent permitted by law, will not be
released under the Freedom of
Information Act, 5 U.S.C. 552.
ADDRESSES: Send written objections to
U.S. Army Research Laboratory
Technology Transfer Office, RDRL–DPP/
Thomas Mulkern, Building 321 Room
110, Aberdeen Proving Ground, MD
21005–5425.
FOR FURTHER INFORMATION CONTACT:
Thomas Mulkern, (410) 278–0889,
Email: ORTA@arl.army.mil.
SUPPLEMENTARY INFORMATION: None.
Brenda S. Bowen,
Army Federal Register Liaison Officer.
[FR Doc. 2015–15957 Filed 6–29–15; 8:45 am]
BILLING CODE 3710–08–P
DEPARTMENT OF DEFENSE
Office of the Secretary
[Docket ID: DoD–2015–OS–0065]
Proposed Collection; Comment
Request
Office of the Under Secretary of
Defense for Personnel and Readiness,
DoD.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995, the
Office of the Under Secretary of Defense
for Personnel and Readiness announces
a proposed public information
collection and seeks public comment on
the provisions thereof. Comments are
invited on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed information collection; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
asabaliauskas on DSK5VPTVN1PROD with NOTICES
SUMMARY:
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17:34 Jun 29, 2015
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Consideration will be given to all
comments received by August 31, 2015.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Department of Defense, Office
of the Deputy Chief Management
Officer, Directorate of Oversight and
Compliance, Regulatory and Audit
Matters Office, 9010 Defense Pentagon,
Washington, DC 20301–9010.
Instructions: All submissions received
must include the agency name, docket
number and title for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information. Any associated form(s) for
this collection may be located within
this same electronic docket and
downloaded for review/testing. Follow
the instructions at https://
www.regulations.gov for submitting
comments. Please submit comments on
any given form identified by docket
number, form number, and title.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection or to
obtain a copy of the proposal and
associated collection instruments,
please write to the Office of Family
Readiness Policy, ATTN: Program
Manager, Spouse Education & Career
Opportunities Program, 4800 Mark
Center Drive Suite 03G15, Alexandria,
VA 22350–2300.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB
Number: Spouse Education and Career
Opportunities Program (SECO); OMB
Control Number 0704–XXXX.
Needs and Uses: This information
collection requirement is necessary to
allow eligible military spouses to access
education and employment resources.
Affected Public: Individuals or
households.
Annual Burden Hours: 19,500.
Number of Respondents: 26,000.
Responses per Respondent: 1.
Annual Responses: 26,000.
Average Burden per Response: 45
minutes.
Frequency: On occasion.
The DoD Spouse Education and
Career Opportunities (SECO) Program is
the primary source of education, career
and employment counseling for all
military spouses who are seeking postDATES:
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secondary education, training, licenses
and credentials needed for portable
career employment. The SECO system
delivers the resources and tools
necessary to assist spouses of service
members with career exploration/
discovery, career education and
training, employment readiness, and
career connections at any point within
the spouse career lifecycle.
Dated: June 25, 2015.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2015–16004 Filed 6–29–15; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF DEFENSE
Office of the Secretary
[Docket ID: DoD–2015–HA–0066]
Proposed Collection; Comment
Request
Office of the Assistant
Secretary of Defense for Health Affairs,
DoD.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995, the
Office of the Assistant Secretary of
Defense for Health Affairs announces a
proposed public information collection
and seeks public comment on the
provisions thereof. Comments are
invited on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed information collection; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
DATES: Consideration will be given to all
comments received by August 31, 2015.
ADDRESSES: You may submit comments,
identified by docket number and title,
by any of the following methods:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Department of Defense, Office
of the Deputy Chief Management
Officer, Directorate of Oversight and
Compliance, Regulatory and Audit
Matters Office, 9010 Defense Pentagon,
Washington, DC 20301–9010.
Instructions: All submissions received
must include the agency name, docket
SUMMARY:
E:\FR\FM\30JNN1.SGM
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Federal Register / Vol. 80, No. 125 / Tuesday, June 30, 2015 / Notices
asabaliauskas on DSK5VPTVN1PROD with NOTICES
number and title for this Federal
Register document. The general policy
for comments and other submissions
from members of the public is to make
these submissions available for public
viewing on the Internet at https://
www.regulations.gov as they are
received without change, including any
personal identifiers or contact
information. Any associated form(s) for
this collection may be located within
this same electronic docket and
downloaded for review/testing. Follow
the instructions at https://
www.regulations.gov for submitting
comments. Please submit comments on
any given form identified by docket
number, form number, and title.
FOR FURTHER INFORMATION CONTACT: To
request more information on this
proposed information collection or to
obtain a copy of the proposal and
associated collection instruments,
please write to the Naval Health
Research Center, Deployment Health
Research Department, ATTN: LCDR
Rachel Lee, 140 Sylvester Rd., San
Diego, CA 92106–3521 or call (619)
553–8983.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB
Number: ACAM2000® Myopericarditis
Registry; OMB Control Number 0720–
0054.
Needs and Uses: The information
collection requirement is necessary to
address Food and Drug Administration
requirements to establish several Phase
IV post-licensure studies to evaluate the
long-term safety of ACAM2000®
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smallpox vaccine. Among the required
post-licensure studies is the
establishment of a myopericarditis
registry. The ACAM2000®
Myopericarditis Registry is designed to
study the natural history of
myopericarditis following receipt of the
ACAM2000® vaccine, including
evaluating factors that may influence
disease prognosis, thus addressing the
FDA post-licensure requirement and
ensuring the continued licensing of this
vaccine.
Affected Public: Individuals or
households; federal government.
Annual Burden Hours: 10.
Number of Respondents: 10.
Responses per Respondent: 2.
Average Burden per Response: 30
minutes.
Frequency: Semi-annually.
Eligible respondents are civilians who
are former Active Duty or active Guard/
Reserve in the U.S. Military that
received the ACACM2000® smallpox
vaccine while in the military and
subsequently developed signs or
symptoms of myopericarditis. The
information collected will illuminate
the natural history of post-vaccine
myopericarditis and evaluate factors
that may influence disease prognosis.
Inclusion of civilians who were
formerly in the military in addition to
current military members is imperative
in order to obtain information on those
who may have separated from the
military due to their medical condition.
Conducting this Registry will ensure the
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37241
continued licensure of this military
relevant vaccine.
Dated: June 25, 2015.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
[FR Doc. 2015–16014 Filed 6–29–15; 8:45 am]
BILLING CODE 5001–06–P
DEPARTMENT OF DEFENSE
Office of the Secretary
[Transmittal No. 15–41]
36(b)(1) Arms Sales Notification
Defense Security Cooperation
Agency, Department of Defense.
ACTION: Notice.
AGENCY:
The Department of Defense is
publishing the unclassified text of a
section 36(b)(1) arms sales notification.
This is published to fulfill the
requirements of section 155 of Public
Law 104–164 dated July 21, 1996.
FOR FURTHER INFORMATION CONTACT: Ms.
B. English, DSCA/DBO/CFM, (703) 601–
3740.
The following is a copy of a letter to
the Speaker of the House of
Representatives, Transmittal 15–41 with
attached Policy Justification and
Sensitivity of Technology.
SUMMARY:
Dated: June 24, 2015.
Aaron Siegel,
Alternate OSD Federal Register Liaison
Officer, Department of Defense.
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]]>Agencies
[Federal Register Volume 80, Number 125 (Tuesday, June 30, 2015)]
[Notices]
[Pages 37240-37241]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-16014]
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DEPARTMENT OF DEFENSE
Office of the Secretary
[Docket ID: DoD-2015-HA-0066]
Proposed Collection; Comment Request
AGENCY: Office of the Assistant Secretary of Defense for Health
Affairs, DoD.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act of 1995, the
Office of the Assistant Secretary of Defense for Health Affairs
announces a proposed public information collection and seeks public
comment on the provisions thereof. Comments are invited on: (a) Whether
the proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed information collection;
(c) ways to enhance the quality, utility, and clarity of the
information to be collected; and (d) ways to minimize the burden of the
information collection on respondents, including through the use of
automated collection techniques or other forms of information
technology.
DATES: Consideration will be given to all comments received by August
31, 2015.
ADDRESSES: You may submit comments, identified by docket number and
title, by any of the following methods:
Federal eRulemaking Portal: https://www.regulations.gov.
Follow the instructions for submitting comments.
Mail: Department of Defense, Office of the Deputy Chief
Management Officer, Directorate of Oversight and Compliance, Regulatory
and Audit Matters Office, 9010 Defense Pentagon, Washington, DC 20301-
9010.
Instructions: All submissions received must include the agency
name, docket
[[Page 37241]]
number and title for this Federal Register document. The general policy
for comments and other submissions from members of the public is to
make these submissions available for public viewing on the Internet at
https://www.regulations.gov as they are received without change,
including any personal identifiers or contact information. Any
associated form(s) for this collection may be located within this same
electronic docket and downloaded for review/testing. Follow the
instructions at https://www.regulations.gov for submitting comments.
Please submit comments on any given form identified by docket number,
form number, and title.
FOR FURTHER INFORMATION CONTACT: To request more information on this
proposed information collection or to obtain a copy of the proposal and
associated collection instruments, please write to the Naval Health
Research Center, Deployment Health Research Department, ATTN: LCDR
Rachel Lee, 140 Sylvester Rd., San Diego, CA 92106-3521 or call (619)
553-8983.
SUPPLEMENTARY INFORMATION:
Title; Associated Form; and OMB Number: ACAM2000[supreg]
Myopericarditis Registry; OMB Control Number 0720-0054.
Needs and Uses: The information collection requirement is necessary
to address Food and Drug Administration requirements to establish
several Phase IV post-licensure studies to evaluate the long-term
safety of ACAM2000[supreg] smallpox vaccine. Among the required post-
licensure studies is the establishment of a myopericarditis registry.
The ACAM2000[supreg] Myopericarditis Registry is designed to study the
natural history of myopericarditis following receipt of the
ACAM2000[supreg] vaccine, including evaluating factors that may
influence disease prognosis, thus addressing the FDA post-licensure
requirement and ensuring the continued licensing of this vaccine.
Affected Public: Individuals or households; federal government.
Annual Burden Hours: 10.
Number of Respondents: 10.
Responses per Respondent: 2.
Average Burden per Response: 30 minutes.
Frequency: Semi-annually.
Eligible respondents are civilians who are former Active Duty or
active Guard/Reserve in the U.S. Military that received the
ACACM2000[supreg] smallpox vaccine while in the military and
subsequently developed signs or symptoms of myopericarditis. The
information collected will illuminate the natural history of post-
vaccine myopericarditis and evaluate factors that may influence disease
prognosis. Inclusion of civilians who were formerly in the military in
addition to current military members is imperative in order to obtain
information on those who may have separated from the military due to
their medical condition. Conducting this Registry will ensure the
continued licensure of this military relevant vaccine.
Dated: June 25, 2015.
Aaron Siegel,
Alternate OSD Federal Register Liaison Officer, Department of Defense.
[FR Doc. 2015-16014 Filed 6-29-15; 8:45 am]
BILLING CODE 5001-06-P
