Proposed Information Collection Activity; Social Services Block Grant (SSBG) Post-Expenditure Report, Pre-Expenditure Report, and Intended Use Plan, 79185-79186 [2020-27015]

Download as PDF 79185 jbell on DSKJLSW7X2PROD with NOTICES Federal Register / Vol. 85, No. 237 / Wednesday, December 9, 2020 / Notices written views, recommendations, and data. Please note that comments received, including attachments and other supporting materials are part of the public record and are subject to public disclosure. Do not include any information in your comment or supporting materials that you consider confidential or inappropriate for public disclosure. If you include your name, contact information, or other information that identifies you in the body of your comments, that information will be on public display. CDC will review all submissions and may choose to redact, or withhold, submissions containing private or proprietary information such as Social Security numbers, medical information, inappropriate language, or duplicate/ near duplicate examples of a mass-mail campaign. CDC will carefully consider all comments submitted into the docket. 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Kalwant Smagh, Director, Strategic Business Initiatives Unit, Office of the Chief Operating Officer, Centers for Disease Control and Prevention. [FR Doc. 2020–27133 Filed 12–7–20; 4:15 pm] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families [OMB No. 0970–0234] Proposed Information Collection Activity; Social Services Block Grant (SSBG) Post-Expenditure Report, PreExpenditure Report, and Intended Use Plan 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 revision to the Social Services Block Grant (SSBG) PostExpenditure Report, Pre-Expenditure Report, and Intended Use Plan (OMB #0970–0234), previously titled, ‘‘Social Services Block Grant (SSBG) PostExpenditure Report’’). ACF is proposing to expand the information collection to include the collection of states’ Intended Use Plans and retitle the information collection to clarify the role of the Pre-Expenditure Report. DATES: Comments due within 60 days of publication. In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, ACF is soliciting public comment on the specific aspects of the information collection described above. ADDRESSES: Copies of the proposed collection of information can be obtained and comments may be forwarded by emailing infocollection@ acf.hhs.gov. Alternatively, copies can also be obtained by writing to the SUMMARY: Administration for Children and Families, Office of Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington, DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or written, should be identified by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: On an annual basis, states and territories are required to submit the following reports: (1) An Intended Use Plan that provides data and narrative descriptions related to the state’s SSBG program. The Intended Use Plan includes details about the delivery of SSBG services and the state agency administering the SSBG Program. ACF is proposing to expand the currently approved information collection to include collection of states’ Intended Use Plans. Grantees are required to submit their Intended Use Plans no less than 30 days prior to the start of the budget period covered by the report. (2) A Pre-Expenditure Report that demonstrates the state’s anticipated allocation of SSBG funding among the 29 pre-defined SSBG service categories. Historically, states have submitted this report using the Post-Expenditure Report Form, and the associated burden is included in the currently approved information collection. Grantees are required to submit their PreExpenditure Report no less than 30 days prior to the start of the budget period covered by the report. (3) A PostExpenditure Report that details the state’s actual use of SSBG funding among 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. 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 This request is specific to the Intended Use Plan. Currently approved materials and associated burden can be found at: https://www.reginfo.gov/ public/do/PRAViewICR?ref_nbr= 202011-0970-006. Instrument Annual number of respondents Annual number of responses per respondent Average burden hours per response Total/annual burden hours Intended Use Plan ................................................................................... 56 1 40 2,240 VerDate Sep<11>2014 16:16 Dec 08, 2020 Jkt 253001 PO 00000 Frm 00024 Fmt 4703 Sfmt 4703 E:\FR\FM\09DEN1.SGM 09DEN1 79186 Federal Register / Vol. 85, No. 237 / Wednesday, December 9, 2020 / Notices Estimated Total Annual Burden Hours: 2,240. Comments: The Department specifically requests comments 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 collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Authority: 42 U.S.C. 1397 through 1397e. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2020–27015 Filed 12–8–20; 8:45 am] BILLING CODE 4184–24–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2014–N–1076] Agency Information Collection Activities; Proposed Collection; Comment Request; Formal Dispute Resolution: Scientific and Technical Issues Related to Pharmaceutical Current Good Manufacturing Practice AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA, Agency, or we) is announcing an opportunity for public comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on the information collection pertaining to Formal Dispute Resolution: Scientific and Technical Issues Related to Pharmaceutical Current Good Manufacturing Practice. DATES: Submit either electronic or written comments on the collection of information by February 8, 2021. jbell on DSKJLSW7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 16:16 Dec 08, 2020 Jkt 253001 You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before February 8, 2021. The https://www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of February 8, 2021. 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. ADDRESSES: 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– 2014–N–1076 for ‘‘Agency Information Collection Activities; Proposed Collection; Comment Request; Guidance for Industry on Formal Dispute PO 00000 Frm 00025 Fmt 4703 Sfmt 4703 Resolution: Scientific and Technical Issues Related to Pharmaceutical Current Good Manufacturing Practice.’’ 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, 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 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. FOR FURTHER INFORMATION CONTACT: Domini Bean, Office of Operations, Food and Drug Administration, Three White Flint North, 10A–12M, 11601 Landsdown St., North Bethesda, MD 20852, 301–796–5733, PRAStaff@ fda.hhs.gov. SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501–3521), Federal E:\FR\FM\09DEN1.SGM 09DEN1

Agencies

[Federal Register Volume 85, Number 237 (Wednesday, December 9, 2020)]
[Notices]
[Pages 79185-79186]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-27015]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families

[OMB No. 0970-0234]


Proposed Information Collection Activity; Social Services Block 
Grant (SSBG) Post-Expenditure Report, Pre-Expenditure Report, and 
Intended Use Plan

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 revision to the Social Services Block Grant (SSBG) Post-
Expenditure Report, Pre-Expenditure Report, and Intended Use Plan (OMB 
#0970-0234), previously titled, ``Social Services Block Grant (SSBG) 
Post-Expenditure Report''). ACF is proposing to expand the information 
collection to include the collection of states' Intended Use Plans and 
retitle the information collection to clarify the role of the Pre-
Expenditure Report.

DATES: Comments due within 60 days of publication. In compliance with 
the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction 
Act of 1995, ACF is soliciting public comment on the specific aspects 
of the information collection described above.

ADDRESSES: Copies of the proposed collection of information can be 
obtained and comments may be forwarded by emailing 
[email protected]. Alternatively, copies can also be obtained 
by writing to the Administration for Children and Families, Office of 
Planning, Research, and Evaluation (OPRE), 330 C Street SW, Washington, 
DC 20201, Attn: ACF Reports Clearance Officer. All requests, emailed or 
written, should be identified by the title of the information 
collection.

SUPPLEMENTARY INFORMATION: 
    Description: On an annual basis, states and territories are 
required to submit the following reports: (1) An Intended Use Plan that 
provides data and narrative descriptions related to the state's SSBG 
program. The Intended Use Plan includes details about the delivery of 
SSBG services and the state agency administering the SSBG Program. ACF 
is proposing to expand the currently approved information collection to 
include collection of states' Intended Use Plans. Grantees are required 
to submit their Intended Use Plans no less than 30 days prior to the 
start of the budget period covered by the report. (2) A Pre-Expenditure 
Report that demonstrates the state's anticipated allocation of SSBG 
funding among the 29 pre-defined SSBG service categories. Historically, 
states have submitted this report using the Post-Expenditure Report 
Form, and the associated burden is included in the currently approved 
information collection. Grantees are required to submit their Pre-
Expenditure Report no less than 30 days prior to the start of the 
budget period covered by the report. (3) A Post-Expenditure Report that 
details the state's actual use of SSBG funding among 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.
    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

    This request is specific to the Intended Use Plan. Currently 
approved materials and associated burden can be found at: https://www.reginfo.gov/public/do/PRAViewICR?ref_nbr=202011-0970-006.

----------------------------------------------------------------------------------------------------------------
                                                            Annual number of   Average burden
               Instrument                 Annual number of    responses per       hours per       Total/annual
                                             respondents       respondent         response        burden hours
----------------------------------------------------------------------------------------------------------------
Intended Use Plan.......................               56                 1                40             2,240
----------------------------------------------------------------------------------------------------------------


[[Page 79186]]

    Estimated Total Annual Burden Hours: 2,240.
    Comments: The Department specifically requests comments 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 collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

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

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2020-27015 Filed 12-8-20; 8:45 am]
BILLING CODE 4184-24-P