Announcement of Intent To Issue One OPDIV-Initiated Supplement to BCFS Health and Human Services Under the Standing Announcement for Residential (Shelter) Services for Unaccompanied Children, HHS-2017-ACF-ORR-ZU-1132, 7726-7727 [2018-03583]

Download as PDF 7726 Federal Register / Vol. 83, No. 36 / Thursday, February 22, 2018 / Notices daltland on DSKBBV9HB2PROD with NOTICES directed to take every reasonable step to solicit comment. In determining whether to approve a collection of information, the Board will consider all comments received from the public and other agencies. Request for Comment on Information Collection Proposal The Board invites public comment on the following information collection, which is being reviewed under authority delegated by the OMB under the PRA. Comments are invited on the following: a. Whether the proposed collection of information is necessary for the proper performance of the Federal Reserve’s functions; including whether the information has practical utility; b. The accuracy of the Federal Reserve’s estimate of the burden of the proposed information collection, including the validity of the methodology and assumptions used; c. Ways to enhance the quality, utility, and clarity of the information to be collected; d. Ways to minimize the burden of information collection on respondents, including through the use of automated collection techniques or other forms of information technology; and e. Estimates of capital or startup costs and costs of operation, maintenance, and purchase of services to provide information. At the end of the comment period, the comments and recommendations received will be analyzed to determine the extent to which the Federal Reserve should modify the proposal prior to giving final approval. Proposal to approve under OMB delegated authority the extension for three years, without revision, of the following report: Report title: Quarterly Report of Assets and Liabilities of Large Foreign Offices of U.S. Banks. Agency form number: FR 2502q. OMB control number: 7100–0079. Frequency: Quarterly. Respondents: U.S. commercial banks, bank holding companies, including financial holding companies, and banking Edge and agreement corporations (U.S. banks) for their large branches and banking subsidiaries that are located in the United Kingdom or the Caribbean. Estimated number of respondents: 27. Estimated average hours per response: 1. Estimated annual burden hours: 108. General description of report: The FR 2502q collects, for each reporting office, claims on and liabilities to residents of the United States and of all countries as VerDate Sep<11>2014 20:10 Feb 21, 2018 Jkt 244001 of each quarter-end. Additional details ` are collected about positions vis-a-vis ` U.S. residents. Positions vis-a-vis other non-U.S. offices of the parent bank and positions arising from derivatives contracts are also broken out. The data are used in constructing a piece of the Financial Accounts of the United States that are compiled by the Board and in preparing the U.S. International Transactions Accounts and the International Investment Position that are compiled by the Bureau for Economic Analysis (BEA), an agency of the Department of Commerce. Legal authorization and confidentiality: The Board is authorized to collect the information in the 2502q from (1) bank holding companies pursuant to section 5 of the Bank Holding Company Act (12 U.S.C. 1844(c)), which authorizes the Board to require a bank holding company and any subsidiary to submit reports, (2) Edge and agreement corporations pursuant to sections 25(7) and 25A(17) of the Federal Reserve Act (‘‘FRA’’) (12 U.S.C. 604a and 625), which authorize the Board to require Edge and agreement corporations to make reports to the Board, and (3) depository institutions pursuant to section 11(a)(2) of the FRA (12 U.S.C. 248(a)(2)), which authorizes the Board to require reports from each member bank as it may deem necessary and authorizes the Board to prescribe reports of liabilities and assets from insured depository institutions to enable the Board to discharge its responsibility to monitor and control monetary and credit aggregates. The FR 2502q report is mandatory. The information from this collection would not be accorded confidential treatment because release of the information is not likely to result in substantial harm to the competitive position of the respondents. If confidential treatment is requested by a respondent, the Board will review the request to determine if confidential treatment is appropriate. Board of Governors of the Federal Reserve System, February 15, 2018. Ann E. Misback, Secretary of the Board. [FR Doc. 2018–03549 Filed 2–21–18; 8:45 am] BILLING CODE 6210–01–P PO 00000 Frm 00073 Fmt 4703 Sfmt 4703 DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [CFDA Number 93.676] Announcement of Intent To Issue One OPDIV-Initiated Supplement to BCFS Health and Human Services Under the Standing Announcement for Residential (Shelter) Services for Unaccompanied Children, HHS–2017– ACF–ORR–ZU–1132 Unaccompanied Alien Children’s (UAC) Program, Office of Refugee Resettlement (ORR), Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS). ACTION: Notice of intent to issue one OPDIV-Initiated Supplement to BCFS Health and Human Services, San Antonio, TX under the UAC Program. AGENCY: ACF, ORR, announces the issuance of one OPDIV-Initiated Supplement to BCFS Health and Human Services, San Antonio, TX in the amount of $15,000,000. ORR has been identifying additional capacity to provide shelter for potential increases in apprehensions of Unaccompanied Children at the U.S. Southern Border. Planning for increased shelter capacity is a prudent step to ensure that ORR is able to meet its responsibility, by law, to provide shelter for Unaccompanied Alien Children referred to its care by the Department of Homeland Security (DHS). To ensure sufficient capacity to provide shelter to unaccompanied children referred to HHS, BCFS proposed to provide ORR with 450 beds in an expedited manner. DATES: Supplemental award funds will support activities for sixty days after activation. SUMMARY: FOR FURTHER INFORMATION CONTACT: Jallyn Sualog, Director, Division of Children’s Services, Office of Refugee Resettlement, 330 Street SW, Washington, DC 20447. Phone: 202– 401–4997. Email: DCSProgram@ acf.hhs.gov. ORR is continuously monitoring its capacity to shelter the unaccompanied children referred to HHS, as well as the information received from interagency partners, to inform any future decisions or actions. ORR has specific requirements for the provision of services. Award recipients must have the infrastructure, licensing, experience, and appropriate level of SUPPLEMENTARY INFORMATION: E:\FR\FM\22FEN1.SGM 22FEN1 Federal Register / Vol. 83, No. 36 / Thursday, February 22, 2018 / Notices trained staff to meet those requirements. The expansion of the existing program and its services through this supplemental award is a key strategy for ORR to be prepared to meet its responsibility to provide shelter for Unaccompanied Children referred to its care by DHS and so that the U.S. Border Patrol can continue its vital national security mission to prevent illegal migration, trafficking, and protect the borders of the United States. Statutory Authority: This program is authorized by— (A) Section 462 of the Homeland Security Act of 2002, which in March 2003, transferred responsibility for the care and custody of Unaccompanied Alien Children from the Commissioner of the former Immigration and Naturalization Service (INS) to the Director of ORR of the Department of Health and Human Services (HHS). (B) The Flores Settlement Agreement, Case No. CV85–4544RJK (C. D. Cal. 1996), as well as the William Wilberforce Trafficking Victims Protection Reauthorization Act of 2008 (Pub.L. 110–457), which authorizes post release services under certain conditions to eligible children. All programs must comply with the Flores Settlement Agreement, Case No. CV85– 4544–RJK (C.D. Cal. 1996), pertinent regulations and ORR policies and procedures. Elizabeth Leo, Grants Policy Specialist, Division of Grants Policy, Office of Administration. [FR Doc. 2018–03583 Filed 2–21–18; 8:45 am] BILLING CODE 4184–45–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Electronic Submissions Food and Drug Administration [Docket No. FDA–2018–N–0140] Peripheral and Central Nervous System Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments AGENCY: Food and Drug Administration, HHS. Notice, establishment of a public docket; request for comments. ACTION: The Food and Drug Administration (FDA) announces a forthcoming public advisory committee meeting of the Peripheral and Central Nervous System Drugs Advisory Committee. The general function of the committee is to provide advice and recommendations to FDA on regulatory issues. The meeting will be open to the daltland on DSKBBV9HB2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 20:10 Feb 21, 2018 Jkt 244001 public. FDA is establishing a docket for public comment on this document. DATES: The meeting will be held on April 19, 2018, from 8 a.m. to 12:30 p.m. ADDRESSES: FDA White Oak Campus, 10903 New Hampshire Ave., Bldg. 31 Conference Center, the Great Room (Rm. 1503), Silver Spring, MD 20993–0002. Answers to commonly asked questions including information regarding special accommodations due to a disability, visitor parking, and transportation may be accessed at: https://www.fda.gov/ AdvisoryCommittees/ AboutAdvisoryCommittees/ ucm408555.htm. FDA is establishing a docket for public comment on this meeting. The docket number is FDA–2018–N–0140. The docket will close on April 18, 2018. Submit either electronic or written comments on this public meeting by April 18, 2018. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before April 18, 2018. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time at the end of April 18, 2018. Comments received by mail/hand 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. Comments received on or before April 5, 2018, will be provided to the committee. Comments received after that date will be taken into consideration by FDA. You may submit comments as follows: 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. PO 00000 Frm 00074 Fmt 4703 Sfmt 4703 7727 • 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–0140 for ‘‘Peripheral and Central Nervous System Drugs Advisory Committee; Notice of Meeting; Establishment of a Public Docket; Request for Comments.’’ Received comments, those filed in a timely manner (see ADDRESSES), will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at https://www.regulations.gov or at the Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ FDA will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/ blacked out, will be available for public viewing and posted on https:// www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify the information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For E:\FR\FM\22FEN1.SGM 22FEN1

Agencies

[Federal Register Volume 83, Number 36 (Thursday, February 22, 2018)]
[Notices]
[Pages 7726-7727]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-03583]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

[CFDA Number 93.676]


Announcement of Intent To Issue One OPDIV-Initiated Supplement to 
BCFS Health and Human Services Under the Standing Announcement for 
Residential (Shelter) Services for Unaccompanied Children, HHS-2017-
ACF-ORR-ZU-1132

AGENCY: Unaccompanied Alien Children's (UAC) Program, Office of Refugee 
Resettlement (ORR), Administration for Children and Families (ACF), 
U.S. Department of Health and Human Services (HHS).

ACTION: Notice of intent to issue one OPDIV-Initiated Supplement to 
BCFS Health and Human Services, San Antonio, TX under the UAC Program.

-----------------------------------------------------------------------

SUMMARY: ACF, ORR, announces the issuance of one OPDIV-Initiated 
Supplement to BCFS Health and Human Services, San Antonio, TX in the 
amount of $15,000,000.
    ORR has been identifying additional capacity to provide shelter for 
potential increases in apprehensions of Unaccompanied Children at the 
U.S. Southern Border. Planning for increased shelter capacity is a 
prudent step to ensure that ORR is able to meet its responsibility, by 
law, to provide shelter for Unaccompanied Alien Children referred to 
its care by the Department of Homeland Security (DHS).
    To ensure sufficient capacity to provide shelter to unaccompanied 
children referred to HHS, BCFS proposed to provide ORR with 450 beds in 
an expedited manner.

DATES: Supplemental award funds will support activities for sixty days 
after activation.

FOR FURTHER INFORMATION CONTACT: Jallyn Sualog, Director, Division of 
Children's Services, Office of Refugee Resettlement, 330 Street SW, 
Washington, DC 20447. Phone: 202-401-4997. Email: 
[email protected].

SUPPLEMENTARY INFORMATION: ORR is continuously monitoring its capacity 
to shelter the unaccompanied children referred to HHS, as well as the 
information received from interagency partners, to inform any future 
decisions or actions.
    ORR has specific requirements for the provision of services. Award 
recipients must have the infrastructure, licensing, experience, and 
appropriate level of

[[Page 7727]]

trained staff to meet those requirements. The expansion of the existing 
program and its services through this supplemental award is a key 
strategy for ORR to be prepared to meet its responsibility to provide 
shelter for Unaccompanied Children referred to its care by DHS and so 
that the U.S. Border Patrol can continue its vital national security 
mission to prevent illegal migration, trafficking, and protect the 
borders of the United States.
    Statutory Authority: This program is authorized by--
    (A) Section 462 of the Homeland Security Act of 2002, which in 
March 2003, transferred responsibility for the care and custody of 
Unaccompanied Alien Children from the Commissioner of the former 
Immigration and Naturalization Service (INS) to the Director of ORR of 
the Department of Health and Human Services (HHS).
    (B) The Flores Settlement Agreement, Case No. CV85-4544RJK (C. D. 
Cal. 1996), as well as the William Wilberforce Trafficking Victims 
Protection Reauthorization Act of 2008 (Pub.L. 110-457), which 
authorizes post release services under certain conditions to eligible 
children. All programs must comply with the Flores Settlement 
Agreement, Case No. CV85-4544-RJK (C.D. Cal. 1996), pertinent 
regulations and ORR policies and procedures.

Elizabeth Leo,
Grants Policy Specialist, Division of Grants Policy, Office of 
Administration.
[FR Doc. 2018-03583 Filed 2-21-18; 8:45 am]
 BILLING CODE 4184-45-P