Submission for OMB Review; Social Services Block Grant (SSBG) Post-Expenditure Report (OMB #0970-0234), 74344-74345 [2020-25639]

Download as PDF 74344 Federal Register / Vol. 85, No. 225 / Friday, November 20, 2020 / Notices 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 December 21, 2020. A. Federal Reserve Bank of Cleveland (Mary S. Johnson, Vice President), 1455 East Sixth Street, Cleveland, Ohio 44101–2566. Comments can also be sent electronically to Comments.applications@clev.frb.org: 1. Dollar Mutual Bancorp, Pittsburgh, Pennsylvania; to acquire Standard AVB Financial Corp. and its subsidiary bank, Standard Bank, PaSB, both of Murrysville, Pennsylvania. Board of Governors of the Federal Reserve System, November 17, 2020. Michele Taylor Fennell, Deputy Associate Secretary of the Board. [FR Doc. 2020–25684 Filed 11–19–20; 8:45 am] BILLING CODE 6210–01–P 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 December 21, 2020. A. Federal Reserve Bank of San Francisco (Sebastian Astrada, Director, Applications), 101 Market Street, San Francisco, California 94105–1579: 1. DMG Bancshares, Inc., Irvine, California; to become a bank holding company by acquiring California First National Bank, also of Irvine, California. Board of Governors of the Federal Reserve System, November 17, 2020. Michele Taylor Fennell, Deputy Associate Secretary of the Board. 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 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 [FR Doc. 2020–25680 Filed 11–19–20; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Social Services Block Grant (SSBG) PostExpenditure Report (OMB #0970–0234) Office of Community Services, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families (ACF) is requesting a 3-year extension of the Social Services Block Grant (SSBG) SUMMARY: Post-Expenditure Report (OMB #0970– 0234, expiration 1/31/2021). Although ACF initially proposed changes (see 85 FR 57863), after reconsideration during the initial comment period, this request is for an extension with no changes. Comments due within 30 days of publication. OMB must make a decision about the collection of information between 30 and 60 days after publication of this document in the Federal Register. Therefore, a comment is best assured of having its full effect if OMB receives it within 30 days of publication. DATES: Written comments and recommendations for the proposed information collection should be sent within 30 days of publication of this notice to www.reginfo.gov/public/do/ PRAMain. Find this particular information collection by selecting ‘‘Currently under 30-day Review—Open for Public Comments’’ or by using the search function. ADDRESSES: SUPPLEMENTARY INFORMATION: Description: On an annual basis, states and territories are required to submit a Post-Expenditure Report that details their use of SSBG funds in each of the 29 service categories. Grantees are required to submit their PostExpenditure Report within 6 months of the end of the period covered by the report. OCS also allows states to use the PostExpenditure Reporting form to provide pre-expenditure data for their annual Intended Use Plans, which provides estimates of the expenditures and number of recipients by service category. Respondents: Agencies that administer the SSBG at the state or territory level, including the 50 States; District of Columbia; Puerto Rico; and the territories of American Samoa, Guam, the Virgin Islands, and the Commonwealth of Northern Mariana Islands. ANNUAL BURDEN ESTIMATES Annual number of respondents khammond on DSKJM1Z7X2PROD with NOTICES Instrument Post-Expenditure Reporting Form ................................................................... Post-Expenditure Reporting Form for Pre-Expenditure Data (funding estimates for the Intended Use Plan) ................................................................ VerDate Sep<11>2014 17:08 Nov 19, 2020 Jkt 253001 PO 00000 Frm 00035 Fmt 4703 Sfmt 4703 Annual number of responses per respondent Average burden hours per response Total/ annual burden hours 56 1 110 6,160 56 1 2 112 E:\FR\FM\20NON1.SGM 20NON1 Federal Register / Vol. 85, No. 225 / Friday, November 20, 2020 / Notices Estimated Total Annual Burden Hours: 6,272. Authority: 42 U.S.C. 1397 through 1397e. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–25639 Filed 11–19–20; 8:45 am] BILLING CODE 4184–24–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2011–D–0611] Biosimilarity and Interchangeability: Additional Draft Q&As on Biosimilar Development and the Biologics Price Competition and Innovation Act of 2009; 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 draft guidance for industry entitled ‘‘Biosimilarity and Interchangeability: Additional Draft Q&As on Biosimilar Development and the BPCI Act.’’ The question and answer (Q&A) format is intended to inform prospective applicants and facilitate the development of proposed biosimilars and proposed interchangeable biosimilars, as well as to describe FDA’s interpretation of certain statutory requirements added by the Biologics Price Competition and Innovation Act of 2009 (BPCI Act). This draft guidance document provides new Q&As. It does not replace the draft guidance document entitled ‘‘New and Revised Draft Q&As on Biosimilar Development and the BPCI Act (Revision 2),’’ issued December 12, 2018. DATES: Submit either electronic or written comments on the draft guidance by January 19, 2021 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: khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: 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 VerDate Sep<11>2014 17:08 Nov 19, 2020 Jkt 253001 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– 2011–D–0611 for ‘‘Biosimilarity and Interchangeability: Additional Draft Q&As on Biosimilar Development and the BPCI Act.’’ 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. • 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 PO 00000 Frm 00036 Fmt 4703 Sfmt 4703 74345 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 this 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. FOR FURTHER INFORMATION CONTACT: Sandra Benton, Center for Drug Evaluation and Research, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 22, Rm. 1132, Silver Spring, MD 20993, 301–796– 1042, sandra.benton@fda.hhs.gov, or 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, stephen.ripley@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background FDA is announcing the availability of a draft guidance for industry entitled ‘‘Biosimilarity and Interchangeability: E:\FR\FM\20NON1.SGM 20NON1

Agencies

[Federal Register Volume 85, Number 225 (Friday, November 20, 2020)]
[Notices]
[Pages 74344-74345]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-25639]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Social Services Block Grant (SSBG) 
Post-Expenditure Report (OMB #0970-0234)

AGENCY: Office of Community Services, Administration for Children and 
Families, HHS.

ACTION: Request for public comment.

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

SUMMARY: The Administration for Children and Families (ACF) is 
requesting a 3-year extension of the Social Services Block Grant (SSBG) 
Post-Expenditure Report (OMB #0970-0234, expiration 1/31/2021). 
Although ACF initially proposed changes (see 85 FR 57863), after 
reconsideration during the initial comment period, this request is for 
an extension with no changes.

DATES: Comments due within 30 days of publication. OMB must make a 
decision about the collection of information between 30 and 60 days 
after publication of this document in the Federal Register. Therefore, 
a comment is best assured of having its full effect if OMB receives it 
within 30 days of publication.

ADDRESSES: Written comments and recommendations for the proposed 
information collection should be sent within 30 days of publication of 
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular 
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.

SUPPLEMENTARY INFORMATION:
    Description: On an annual basis, states and territories are 
required to submit a Post-Expenditure Report that details their use of 
SSBG funds in each of the 29 service categories. Grantees are required 
to submit their Post-Expenditure Report within 6 months of the end of 
the period covered by the report.
    OCS also allows states to use the Post-Expenditure Reporting form 
to provide pre-expenditure data for their annual Intended Use Plans, 
which provides estimates of the expenditures and number of recipients 
by service category.
    Respondents: Agencies that administer the SSBG at the state or 
territory level, including the 50 States; District of Columbia; Puerto 
Rico; and the territories of American Samoa, Guam, the Virgin Islands, 
and the Commonwealth of Northern Mariana Islands.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                   Annual number  Average burden
                   Instrument                      Annual number   of responses      hours per     Total/ annual
                                                  of respondents  per respondent     response      burden hours
----------------------------------------------------------------------------------------------------------------
Post-Expenditure Reporting Form.................              56               1             110           6,160
Post-Expenditure Reporting Form for Pre-                      56               1               2             112
 Expenditure Data (funding estimates for the
 Intended Use Plan).............................
----------------------------------------------------------------------------------------------------------------


[[Page 74345]]

    Estimated Total Annual Burden Hours: 6,272.

    Authority: 42 U.S.C. 1397 through 1397e.

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-25639 Filed 11-19-20; 8:45 am]
BILLING CODE 4184-24-P