Proposed Collection; Comment Request, 37240-37241 [2015-16014]

Download as PDF 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: VerDate Sep<11>2014 17:34 Jun 29, 2015 Jkt 235001 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: PO 00000 Frm 00022 Fmt 4703 Sfmt 4703 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 30JNN1 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® VerDate Sep<11>2014 17:34 Jun 29, 2015 Jkt 235001 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 PO 00000 Frm 00023 Fmt 4703 Sfmt 4703 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. E:\FR\FM\30JNN1.SGM 30JNN1

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
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