Agency Information Collection Activities: Announcement of Board Approval Under Delegated Authority and Submission to OMB, 17849-17850 [2024-05139]

Download as PDF Federal Register / Vol. 89, No. 49 / Tuesday, March 12, 2024 / Notices khammond on DSKJM1Z7X2PROD with NOTICES under the Shipping Act of 1984. Interested parties may submit comments, relevant information, or documents regarding the agreements to the Secretary by email at Secretary@ fmc.gov, or by mail, Federal Maritime Commission, 800 North Capitol Street, Washington, DC 20573. Comments will be most helpful to the Commission if received within 12 days of the date this notice appears in the Federal Register, and the Commission requests that comments be submitted within 7 days on agreements that request expedited review. Copies of agreements are available through the Commission’s website (www.fmc.gov) or by contacting the Office of Agreements at (202) 523– 5793 or tradeanalysis@fmc.gov. Agreement No.: 201421. Agreement Name: Agency Agreement. Parties: Arkas Container Transport SA; Turkon Container Transportation & Shipping, Inc. Filing Party: Wayne Rohde; Cozen O’Connor. Synopsis: The Agreement authorizes Turkon America Inc. to acts as the U.S. agent of Arkas Container Transport S.A. (‘‘Arkas’’) with respect to Arkas’ services in the trades between the U.S. Atlantic Coast on the one hand and countries bordering the Black and Mediterranean Seas, Western Europe, Northern Europe, and West and North Africa. The parties have requested expedited review. Proposed Effective Date: 04/15/2024. Location: https://www2.fmc.gov/ FMC.Agreements.Web/Public/ AgreementHistory/86551. Agreement No.: 012426–007. Agreement Name: The OCEAN Alliance Agreement. Parties: American President Lines, LLC; APL CO. PTE. LTD; CMA CGM S.A.; COSCO Shipping Lines Co., Ltd; Evergreen Line Joint Service Agreement; OOCL (Europe) Limited; Orient Overseas Container Line Limited. Filing Party: Robert Magovern; Cozen O’Connor. Synopsis: This Amendment revises Article 7 to extend the term of the Agreement through March 31, 2032. Proposed Effective Date: 04/15/2024. Location: https://www2.fmc.gov/ FMC.Agreements.Web/Public/ AgreementHistory/1214. Dated: March 6, 2024. Alanna Beck, Federal Register Alternate Liaison Officer. [FR Doc. 2024–05144 Filed 3–11–24; 8:45 am] FEDERAL RESERVE SYSTEM FEDERAL RESERVE SYSTEM Formations of, Acquisitions by, and Mergers of Bank Holding Companies Agency Information Collection Activities: Announcement of Board Approval Under Delegated Authority and Submission to OMB 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 public portions of 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(s) indicated below and at the offices of the Board of Governors. This information may also be obtained on an expedited basis, upon request, by contacting the appropriate Federal Reserve Bank and from the Board’s Freedom of Information Office at https://www.federalreserve.gov/foia/ request.htm. 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 Street and Constitution Avenue NW, Washington, DC 20551–0001, not later than April 11, 2024. A. Federal Reserve Bank of Atlanta (Erien O. Terry, Assistant Vice President) 1000 Peachtree Street NE, Atlanta, Georgia 30309. Comments can also be sent electronically to Applications.Comments@atl.frb.org: 1. FB Bancorp, Inc., New Orleans, Louisiana; to become a bank holding company by acquiring Fidelity Bank, New Orleans, Louisiana, a statechartered mutual savings bank (Bank), in connection with Bank’s conversion from mutual to stock form. Board of Governors of the Federal Reserve System. Michele Taylor Fennell, Deputy Associate Secretary of the Board. [FR Doc. 2024–05236 Filed 3–11–24; 8:45 am] BILLING CODE P BILLING CODE 6730–02–P VerDate Sep<11>2014 19:36 Mar 11, 2024 Jkt 262001 17849 PO 00000 Frm 00041 Fmt 4703 Sfmt 4703 Board of Governors of the Federal Reserve System. SUMMARY: The Board of Governors of the Federal Reserve System (Board) is adopting a proposal to implement the Whistleblower Intake Guide (FR 30; OMB No. 7100–NEW). FOR FURTHER INFORMATION CONTACT: Federal Reserve Board Clearance Officer—Nuha Elmaghrabi—Office of the Chief Data Officer, Board of Governors of the Federal Reserve System, nuha.elmaghrabi@frb.gov, (202) 452–3884. Office of Management and Budget (OMB) Desk Officer for the Federal Reserve Board, Office of Information and Regulatory Affairs, Office of Management and Budget, New Executive Office Building, Room 10235, 725 17th Street NW, Washington, DC 20503, or by fax to (202) 395–6974. SUPPLEMENTARY INFORMATION: On June 15, 1984, OMB delegated to the Board authority under the Paperwork Reduction Act (PRA) to approve and assign OMB control numbers to collections of information conducted or sponsored by the Board. Boardapproved collections of information are incorporated into the official OMB inventory of currently approved collections of information. The OMB inventory, as well as copies of the PRA Submission, supporting statements (which contain more detailed information about the information collections and burden estimates than this notice), and approved collection of information instrument(s) are available at https://www.reginfo.gov/public/do/ PRAMain. These documents are also available on the Federal Reserve Board’s public website at https:// www.federalreserve.gov/apps/ reportingforms/home/review or may be requested from the agency clearance officer, whose name appears above. AGENCY: Final Approval Under OMB Delegated Authority of the Implementation of the Following Information Collection Collection title: Whistleblower Intake Guide. Collection identifier: FR 30. OMB control number: 7100–NEW. Dates: This information collection will be effective April 11, 2024. General description of collection: The Whistleblower Intake Guide collects information regarding alleged misconduct or retaliation by a Board- E:\FR\FM\12MRN1.SGM 12MRN1 17850 Federal Register / Vol. 89, No. 49 / Tuesday, March 12, 2024 / Notices supervised institution or an affiliated party of such institution. The information collected through the FR 30 assists in the Board’s supervision of financial institutions. Frequency: Event-generated. Respondents: Employees of Boardsupervised entities and members of the public. Total estimated number of respondents: 5. Estimated average hours per response: 0.5. Total estimated annual burden hours: 3.1 Current actions: On September 8, 2023, the Board published a notice in the Federal Register (88 FR 62084) requesting public comment for 60 days on the implementation of the FR 30. The comment period for this notice expired on November 7, 2023. The Board did not receive any comments. The FR 30 will be implemented as originally proposed. Board of Governors of the Federal Reserve System, March 6, 2024. Michele Taylor Fennell, Deputy Associate Secretary of the Board. [FR Doc. 2024–05139 Filed 3–11–24; 8:45 am] BILLING CODE 6210–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2013–D–0077] Early Alzheimer’s Disease: Developing Drugs for Treatment; Draft 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 revised draft guidance for industry entitled ‘‘Early Alzheimer’s Disease: Developing Drugs for Treatment.’’ This draft guidance is intended to assist sponsors in the clinical development of drugs for the treatment of the stages of sporadic Alzheimer’s disease (AD) that occur before the onset of overt dementia. This draft guidance revises the previous draft guidance for industry of the same name issued on February 16, 2018. khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: 1 More detailed information regarding this collection, including more detailed burden estimates, can be found in the OMB Supporting Statement posted at https://www.federalreserve.gov/ apps/reportingforms/home/review. On the page displayed at the link, you can find the OMB Supporting Statement by referencing the collection identifier, FR 30. VerDate Sep<11>2014 19:36 Mar 11, 2024 Jkt 262001 Submit either electronic or written comments on the draft guidance by May 13, 2024 to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance. ADDRESSES: You may submit comments on any guidance at any time as follows: DATES: Electronic Submissions 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. • 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– 2013–D–0077 for ‘‘Early Alzheimer’s Disease: Developing Drugs for Treatment.’’ 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, 240–402–7500. PO 00000 Frm 00042 Fmt 4703 Sfmt 4703 • 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 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.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.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, 240–402–7500. 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 draft guidance to the Division of Drug Information, Center for Drug Evaluation and Research, Food and Drug Administration, 10001 New Hampshire Ave., Hillandale Building, 4th Floor, Silver Spring, MD 20993– 0002; or the Office of Communication, Outreach, and Development, Center for Biologics Evaluation and Research, 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 that office in processing your requests. See the SUPPLEMENTARY INFORMATION section for electronic access to the draft guidance document. E:\FR\FM\12MRN1.SGM 12MRN1

Agencies

[Federal Register Volume 89, Number 49 (Tuesday, March 12, 2024)]
[Notices]
[Pages 17849-17850]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-05139]


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FEDERAL RESERVE SYSTEM


Agency Information Collection Activities: Announcement of Board 
Approval Under Delegated Authority and Submission to OMB

AGENCY: Board of Governors of the Federal Reserve System.

SUMMARY: The Board of Governors of the Federal Reserve System (Board) 
is adopting a proposal to implement the Whistleblower Intake Guide (FR 
30; OMB No. 7100-NEW).

FOR FURTHER INFORMATION CONTACT: Federal Reserve Board Clearance 
Officer--Nuha Elmaghrabi--Office of the Chief Data Officer, Board of 
Governors of the Federal Reserve System, [email protected], (202) 
452-3884.
    Office of Management and Budget (OMB) Desk Officer for the Federal 
Reserve Board, Office of Information and Regulatory Affairs, Office of 
Management and Budget, New Executive Office Building, Room 10235, 725 
17th Street NW, Washington, DC 20503, or by fax to (202) 395-6974.

SUPPLEMENTARY INFORMATION: On June 15, 1984, OMB delegated to the Board 
authority under the Paperwork Reduction Act (PRA) to approve and assign 
OMB control numbers to collections of information conducted or 
sponsored by the Board. Board-approved collections of information are 
incorporated into the official OMB inventory of currently approved 
collections of information. The OMB inventory, as well as copies of the 
PRA Submission, supporting statements (which contain more detailed 
information about the information collections and burden estimates than 
this notice), and approved collection of information instrument(s) are 
available at https://www.reginfo.gov/public/do/PRAMain. These documents 
are also available on the Federal Reserve Board's public website at 
https://www.federalreserve.gov/apps/reportingforms/home/review or may 
be requested from the agency clearance officer, whose name appears 
above.

Final Approval Under OMB Delegated Authority of the Implementation of 
the Following Information Collection

    Collection title: Whistleblower Intake Guide.
    Collection identifier: FR 30.
    OMB control number: 7100-NEW.
    Dates: This information collection will be effective April 11, 
2024.
    General description of collection: The Whistleblower Intake Guide 
collects information regarding alleged misconduct or retaliation by a 
Board-

[[Page 17850]]

supervised institution or an affiliated party of such institution. The 
information collected through the FR 30 assists in the Board's 
supervision of financial institutions.
    Frequency: Event-generated.
    Respondents: Employees of Board-supervised entities and members of 
the public.
    Total estimated number of respondents: 5.
    Estimated average hours per response: 0.5.
    Total estimated annual burden hours: 3.\1\
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    \1\ More detailed information regarding this collection, 
including more detailed burden estimates, can be found in the OMB 
Supporting Statement posted at https://www.federalreserve.gov/apps/reportingforms/home/review. On the page displayed at the link, you 
can find the OMB Supporting Statement by referencing the collection 
identifier, FR 30.
---------------------------------------------------------------------------

    Current actions: On September 8, 2023, the Board published a notice 
in the Federal Register (88 FR 62084) requesting public comment for 60 
days on the implementation of the FR 30. The comment period for this 
notice expired on November 7, 2023. The Board did not receive any 
comments. The FR 30 will be implemented as originally proposed.

    Board of Governors of the Federal Reserve System, March 6, 2024.
Michele Taylor Fennell,
Deputy Associate Secretary of the Board.
[FR Doc. 2024-05139 Filed 3-11-24; 8:45 am]
BILLING CODE 6210-01-P
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