Announcement of Intent To Award Three OPDIV-Initiated Supplements for Grantees Under the Direct Services for Survivors of Torture Program, 52884-52885 [2019-21518]

Download as PDF 52884 Federal Register / Vol. 84, No. 192 / Thursday, October 3, 2019 / Notices Farm Credit Administration, 1501 Farm Credit Drive, McLean, Virginia 22102–5090. Submit attendance requests via email to VisitorRequest@FCA.gov. See SUPPLEMENTARY INFORMATION for further information about attendance requests. FOR FURTHER INFORMATION CONTACT: Dale Aultman, Secretary to the Farm Credit Administration Board, (703) 883–4009, TTY (703) 883–4056. SUPPLEMENTARY INFORMATION: This meeting of the Board will be open to the public (limited space available), and parts will be closed to the public. Please send an email to VisitorRequest@ FCA.gov at least 24 hours before the meeting. In your email include: Name, postal address, entity you are representing (if applicable), and telephone number. You will receive an email confirmation from us. Please be prepared to show a photo identification when you arrive. If you need assistance for accessibility reasons, or if you have any questions, contact Dale Aultman, Secretary to the Farm Credit Administration Board, at (703) 883– 4009. The matters to be considered at the meeting are: ADDRESSES: Open Session A. Approval of Minutes • September 12, 2019 B. New Business • Delegation of Authority to approve De Minimus capital redemption requests C. Closed Session • Office of Secondary Market Oversight Periodic Report 1 Dated: September 30, 2019. Dale Aultman, Secretary, Farm Credit Administration Board. [FR Doc. 2019–21624 Filed 10–1–19; 11:15 am] BILLING CODE 6705–01–P FEDERAL RESERVE SYSTEM Formations of, Acquisitions by, and Mergers of Bank Holding Companies The companies listed in this notice have applied to the Board for approval, pursuant to the Bank Holding Company Act of 1956 (12 U.S.C. 1841 et seq.) (BHC Act), Regulation Y (12 CFR part 225), and all other applicable statutes and regulations to become a bank holding company and/or to acquire the assets or the ownership of, control of, or the power to vote shares of a bank or bank holding company and all of the banks and nonbanking companies owned by the bank holding company, including the companies listed below. The applications listed below, as well as other related filings required by the Board, if any, are available for immediate inspection at the Federal Reserve Bank indicated. The applications will also be available for inspection at the offices of the Board of Governors. Interested persons may express their views in writing on the standards enumerated in the BHC Act (12 U.S.C. 1842(c)). Comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors, Ann E. Misback, Secretary of the Board, 20th and Constitution Avenue NW, Washington, DC 20551–0001, not later than November 4, 2019. A. Federal Reserve Bank of Atlanta (Kathryn Haney, Assistant Vice President) 1000 Peachtree Street NE, Atlanta, Georgia 30309. Comments can also be sent electronically to Applications.Comments@atl.frb.org: 1. Professional Holding Corp., Coral Gables, Florida; to merge with Marquis Bancorp Inc., and thereby indirectly acquire Marquis Bank, both of Coral Gables, Florida. B. Federal Reserve Bank of Boston (Prabal Chakrabarti, Senior Vice President) 600 Atlantic Avenue, Boston, Massachusetts 02210–2204. Comments can also be sent electronically to BOS.SRC.Applications.Comments@ bos.frb.org: 1. GSB Mutual Holding Company and GSB Bancorp, Inc., both of Guilford, Connecticut; to become a mutual holding company and a mid-tier stock bank holding company, respectively, by acquiring The Guilford Savings Bank, Guilford, Connecticut, in connection with the conversion by The Guilford Savings Bank from mutual to stock form. Board of Governors of the Federal Reserve System, September 27, 2019. Yao-Chin Chao, Assistant Secretary of the Board. [FR Doc. 2019–21483 Filed 10–2–19; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [CFDA Number: 93.604] Announcement of Intent To Award Three OPDIV-Initiated Supplements for Grantees Under the Direct Services for Survivors of Torture Program Office of Refugee Resettlement (ORR), Administration for Children and Families (ACF), Department of Health and Human Services (HHS). ACTION: Notice of intent to issue three OPDIV-Initiated Supplements. AGENCY: The ACF, ORR, Division of Refugee Health announces the intent to award three OPDIV-Initiated Supplements in the amount of $67,724 to each of three current grantees providing direct services funded through the Services for Survivors of Torture (SOT) Program. DATES: The proposed period of support for the supplements begins on September 30, 2019, and ends on September 29, 2020. FOR FURTHER INFORMATION CONTACT: Curi Kim, Division Director, Division of Refugee Health, Office of Refugee Resettlement, 330 C Street SW, Washington, DC 20201. Telephone: 202–401–5585. Email: curi.kim@ acf.hhs.gov. SUMMARY: Three grantees that are located in states which have the greatest need for services will receive supplements to enhance their capacity to serve survivors of torture within the scope of their original proposed activities. The table below shows the grantees, location, and supplemental award amount. SUPPLEMENTARY INFORMATION: State Supplement amount Organization City Program for Torture Victims ............................................... Gulf Coast Jewish Family and Community Services, Florida Center for Survivors of Torture. Center for Survivors of Torture .......................................... Los Angeles ....................................................................... Clearwater and Miami ....................................................... CA FL $67,724 67,724 Dallas ................................................................................. TX 67,724 1 Session Closed-Exempt pursuant to 5 U.S.C. Section 552b(c)(8) and (9). VerDate Sep<11>2014 17:22 Oct 02, 2019 Jkt 250001 PO 00000 Frm 00017 Fmt 4703 Sfmt 4703 E:\FR\FM\03OCN1.SGM 03OCN1 Federal Register / Vol. 84, No. 192 / Thursday, October 3, 2019 / Notices Authority: Torture Victims Relief Act of 1998, Section 5(a), Pub. L. 105–320 (22 U.S.C. 2152 note). Elizabeth Leo, Senior Grants Policy Specialist, Division of Grants Policy, Office of Administration. [FR Doc. 2019–21518 Filed 9–30–19; 11:15 am] BILLING CODE 4184–45–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2018–D–3197] Further Testing of Donations That Are Reactive on a Licensed Donor Screening Test for Antibodies to Hepatitis C Virus; Guidance for Industry; Availability AGENCY: Food and Drug Administration, HHS. ACTION: Notice of availability. The Food and Drug Administration (FDA or Agency) is announcing the availability of a final guidance entitled ‘‘Further Testing of Donations that are Reactive on a Licensed Donor Screening Test for Antibodies to Hepatitis C Virus; Guidance for Industry.’’ The guidance document provides blood establishments that collect Whole Blood and blood components, including Source Plasma, with recommendations for further testing of donations that are reactive on a licensed donor screening test for antibodies to hepatitis C virus (anti-HCV). The guidance also provides guidance to blood establishments on how to report the implementation of these recommendations. The guidance updates the recommendations related to the use of an appropriate multiantigen supplemental test contained in ‘‘Guidance for Industry: ‘Lookback’ for Hepatitis C Virus (HCV): Product Quarantine, Consignee Notification, Further Testing, Product Disposition, and Notification of Transfusion Recipients Based on Donor Test Results Indicating Infection with HCV’’ dated December 2010. The guidance announced in this notice finalizes the draft guidance of the same title dated September 2018. DATES: The announcement of the guidance is published in the Federal Register on October 3, 2019. ADDRESSES: You may submit comments on any guidance at any time as follows: SUMMARY: Electronic Submissions Submit electronic comments in the following way: VerDate Sep<11>2014 17:22 Oct 02, 2019 Jkt 250001 • 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. • 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–D–3197 for ‘‘Further Testing of Donations that are Reactive on a Licensed Donor Screening Test for Antibodies to Hepatitis C Virus; Guidance for Industry.’’ Received comments 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.’’ The PO 00000 Frm 00018 Fmt 4703 Sfmt 4703 52885 Agency 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 to 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 this 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 more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https://www.gpo.gov/ fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. You may submit comments on any guidance at any time (see 21 CFR 10.115(g)(5)). Submit written requests for single copies of the guidance to the Office of Communication, Outreach and Development, Center for Biologics Evaluation and Research (CBER), Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 71, Rm. 3128, Silver Spring, MD 20993–0002. Send one self-addressed adhesive label to assist the office in processing your requests. The guidance may also be obtained by mail by calling CBER at 1– 800–835–4709 or 240–402–8010. See the SUPPLEMENTARY INFORMATION section for electronic access to the guidance document. FOR FURTHER INFORMATION CONTACT: Stephen Ripley, Center for Biologics Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 71, Rm. 7301, Silver Spring, MD 20993–0002, 240– 402–7911. SUPPLEMENTARY INFORMATION: I. Background FDA is announcing the availability of a document entitled ‘‘Further Testing of Donations that are Reactive on a E:\FR\FM\03OCN1.SGM 03OCN1

Agencies

[Federal Register Volume 84, Number 192 (Thursday, October 3, 2019)]
[Notices]
[Pages 52884-52885]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-21518]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

[CFDA Number: 93.604]


Announcement of Intent To Award Three OPDIV-Initiated Supplements 
for Grantees Under the Direct Services for Survivors of Torture Program

AGENCY: Office of Refugee Resettlement (ORR), Administration for 
Children and Families (ACF), Department of Health and Human Services 
(HHS).

ACTION: Notice of intent to issue three OPDIV-Initiated Supplements.

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

SUMMARY: The ACF, ORR, Division of Refugee Health announces the intent 
to award three OPDIV-Initiated Supplements in the amount of $67,724 to 
each of three current grantees providing direct services funded through 
the Services for Survivors of Torture (SOT) Program.

DATES: The proposed period of support for the supplements begins on 
September 30, 2019, and ends on September 29, 2020.

FOR FURTHER INFORMATION CONTACT: Curi Kim, Division Director, Division 
of Refugee Health, Office of Refugee Resettlement, 330 C Street SW, 
Washington, DC 20201. Telephone: 202-401-5585. Email: 
[email protected].

SUPPLEMENTARY INFORMATION: Three grantees that are located in states 
which have the greatest need for services will receive supplements to 
enhance their capacity to serve survivors of torture within the scope 
of their original proposed activities. The table below shows the 
grantees, location, and supplemental award amount.

----------------------------------------------------------------------------------------------------------------
                                                                                                    Supplement
               Organization                            City                       State               amount
----------------------------------------------------------------------------------------------------------------
Program for Torture Victims..............  Los Angeles.................  CA                              $67,724
Gulf Coast Jewish Family and Community     Clearwater and Miami........  FL                               67,724
 Services, Florida Center for Survivors
 of Torture.
Center for Survivors of Torture..........  Dallas......................  TX                               67,724
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[[Page 52885]]

    Authority: Torture Victims Relief Act of 1998, Section 5(a), 
Pub. L. 105-320 (22 U.S.C. 2152 note).

Elizabeth Leo,
Senior Grants Policy Specialist, Division of Grants Policy, Office of 
Administration.
[FR Doc. 2019-21518 Filed 9-30-19; 11:15 am]
BILLING CODE 4184-45-P
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