Proposed Information Collection Activity; Administration for Native Americans Annual Data Report (ADR) (OMB #0970-0475), 70845-70846 [2021-26912]

Download as PDF 70845 Federal Register / Vol. 86, No. 236 / Monday, December 13, 2021 / Notices ANNUAL BURDEN ESTIMATES Total number of respondents Data collection activity Number of responses per respondent (each year) Average burden hours per response (in hours) Total annual burden hours Site Visit and Key Informant Data Collection Program director individual interview ............................................................... Program manager/supervisor individual interviews ......................................... Frontline staff interviews .................................................................................. Partner representative interviews .................................................................... Partner survey ................................................................................................. Sustainability survey ........................................................................................ 8 8 16 24 40 126 0.33 0.33 0.33 0.33 0.33 0.42 2 1 1 1 0.42 0.33 5 3 5 8 6 18 18 54 54 18 108 2 33 33 10 1,560 16.5 0.25 0.0167 0.01672 0.033 594 446 30 3 5,560 18 18 1 2 41 144 738 5,184 18 18 16 100 2 100 .625 25 .625 1,125 900 1,000 ........................ ........................ ........................ 15,625 Enrollment, client and service data Semi-annual progress reports ......................................................................... Case enrollment data ...................................................................................... Case closure .................................................................................................... Case closure—prenatal ................................................................................... Service log entries ........................................................................................... Outcome and impact data Administrative Data: Obtain access to administrative data ....................................................... Report administrative data ....................................................................... Standardized instruments: Enter data into local database ................................................................. Review records and submit ...................................................................... Data entry for comparison study sites (16 grantees) ............................... khammond on DSKJM1Z7X2PROD with NOTICES Estimated Total Burden Hours .......................................................... Estimated Total Annual Burden Hours: 15,625. 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: The Child and Family Services Improvement Act of 2006 (Pub. L. 109–288) created the competitive RPG program. The September 30, 2011, passage of the Child and Family Services Improvement and Innovation Act (Pub. L. 112–34) extended funding for the RPG program from federal fiscal year (FFY) 2012 to FFY 2016. In 2018, the president signed the Bipartisan Budget Act of 2018 (Pub. L. 115–123) into law reauthorizing the RPG program VerDate Sep<11>2014 16:50 Dec 10, 2021 Jkt 256001 through FFY 2021 and added a focus on opioid abuse. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2021–26913 Filed 12–10–21; 8:45 am] BILLING CODE 4184–29–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Administration for Native Americans Annual Data Report (ADR) (OMB #0970–0475) Administration for Native Americans, Administration for Children and Families, HHS. ACTION: Request for public comment. AGENCY: The Administration for Children and Families’ (ACF) Administration for Native Americans (ANA) is requesting a 2-year extension to the following information collection: Annual Data Report (ADR) (OMB #0970–0475; expiration date: 2/28/ 2022). There are no changes requested to the form. DATES: Comments due within 60 days of publication. In compliance with the SUMMARY: PO 00000 Frm 00032 Fmt 4703 Sfmt 4703 requirements of the Paperwork Reduction Act of 1995, ACF is soliciting public comment on the specific aspects of the information collection described above. ADDRESSES: You can obtain copies of the proposed collection of information and submit comments by emailing infocollection@acf.hhs.gov. Identify all requests by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: ANA collects the information in the ADR on an annual basis to monitor the performance of grantees and better gauge grantee progress. The majority of grantees submit this information through the Ongoing Progress Report (OMB #0970– 0452), but there is a subset of about 80 grantees who still use the ADR and will continue to use the ADR through the end of their grants. The ADR information collection is conducted in accordance with sec. 811 [42 U.S.C. 2992] of the Native American Programs Act and will allow ANA to report quantifiable results across all program areas. It also provides grantees with parameters for reporting their progress and helps ANA better monitor and determine the effectiveness of their projects. Respondents: Tribal Government, Native non-profit organizations, and E:\FR\FM\13DEN1.SGM 13DEN1 70846 Federal Register / Vol. 86, No. 236 / Monday, December 13, 2021 / Notices Tribal Colleges and Universities receiving ANA funding. ANNUAL BURDEN ESTIMATES Instrument Total number of respondents Annual number of responses per respondent Average burden hours per response Annual burden hours ANA ADR ......................................................................................................... 80 1 1 80 Estimated Total Annual Burden Hours: 80. 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. 2992. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2021–26912 Filed 12–10–21; 8:45 am] BILLING CODE 4184–34–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2021–N–1285] Oncologic 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 Oncologic 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 public. FDA is establishing a docket for public comment on this document. khammond on DSKJM1Z7X2PROD with NOTICES SUMMARY: VerDate Sep<11>2014 17:25 Dec 10, 2021 Jkt 256001 The meeting will be held virtually on February 10, 2022, from 10 a.m. to 3 p.m. Eastern Time. ADDRESSES: Please note that due to the impact of this COVID–19 pandemic, all meeting participants will be joining this advisory committee meeting via an online teleconferencing platform. Answers to commonly asked questions about FDA advisory committee meetings 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–2021–N–1285. The docket will close on February 9, 2022. Submit either electronic or written comments on this public meeting by February 9, 2022. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before February 9, 2022. The https:// www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of February 9, 2022. 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 January 27, 2022, will be provided to the committee. Comments received after that date will be taken into consideration by FDA. In the event that the meeting is cancelled, FDA will continue to evaluate any relevant applications or information, and consider any comments submitted to the docket, as appropriate. You may submit comments 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:// PO 00000 Frm 00033 Fmt 4703 Sfmt 4703 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– 2021–N–1285 for ‘‘Oncologic 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, 240–402–7500. • Confidential Submissions—To submit a comment with confidential E:\FR\FM\13DEN1.SGM 13DEN1

Agencies

[Federal Register Volume 86, Number 236 (Monday, December 13, 2021)]
[Notices]
[Pages 70845-70846]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-26912]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Administration for 
Native Americans Annual Data Report (ADR) (OMB #0970-0475)

AGENCY: Administration for Native Americans, Administration for 
Children and Families, HHS.

ACTION: Request for public comment.

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

SUMMARY: The Administration for Children and Families' (ACF) 
Administration for Native Americans (ANA) is requesting a 2-year 
extension to the following information collection: Annual Data Report 
(ADR) (OMB #0970-0475; expiration date: 2/28/2022). There are no 
changes requested to the form.

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

ADDRESSES: You can obtain copies of the proposed collection of 
information and submit comments by emailing [email protected]. 
Identify all requests by the title of the information collection.

SUPPLEMENTARY INFORMATION: 
    Description: ANA collects the information in the ADR on an annual 
basis to monitor the performance of grantees and better gauge grantee 
progress. The majority of grantees submit this information through the 
On-going Progress Report (OMB #0970-0452), but there is a subset of 
about 80 grantees who still use the ADR and will continue to use the 
ADR through the end of their grants.
    The ADR information collection is conducted in accordance with sec. 
811 [42 U.S.C. 2992] of the Native American Programs Act and will allow 
ANA to report quantifiable results across all program areas. It also 
provides grantees with parameters for reporting their progress and 
helps ANA better monitor and determine the effectiveness of their 
projects.
    Respondents: Tribal Government, Native non-profit organizations, 
and

[[Page 70846]]

Tribal Colleges and Universities receiving ANA funding.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                Annual  number   Average burden
                 Instrument                   Total number of    of responses      hours per      Annual burden
                                                 respondents   per  respondent      response          hours
----------------------------------------------------------------------------------------------------------------
ANA ADR.....................................              80                1                1               80
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 80.
    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. 2992.

Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021-26912 Filed 12-10-21; 8:45 am]
BILLING CODE 4184-34-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.