Submission for OMB Review; Comment Request; Child Care and Development Fund Financial Report (ACF-696) for States and Territories, 64161-64162 [2016-22449]

Download as PDF 64161 Federal Register / Vol. 81, No. 181 / Monday, September 19, 2016 / Notices RPG CROSS-SITE EVALUATION ANNUALIZED BURDEN ESTIMATES—Continued Total number of respondents Data collection activity Service log entries ............................................................... Staff survey .......................................................................... Partner survey ...................................................................... Number of responses per respondent 126 80 80 Average burden hours per response (in hours) 2,340 1 1 Estimated Total burden hours Total Annual burden hours 0.05 0.42 0.33 14,742 33.6 26.4 4,914 11.2 8.8 Data Entry for Outcomes Study Administrative Data: Obtain access to administrative data ........................... Report administrative data ............................................ Standardized instruments: Enter data into local database ...................................... Review records and submit .......................................... 21 21 2 6 18 144 378 18,144 126 6,048 21 21 6 6 112.5 100 14,175 12,600 4,725 4,200 Additional Data Entry for Impact Study Data entry for comparison study sites (7 grantees) ............ 5 1 .25 1,085 361.6 Estimated Total Burden Hours ............................................ ........................ ........................ ........................ ........................ 21,602.77 In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, the Children’s Bureau within the Administration for Children and Families is soliciting public comment on the specific aspects of the information collection described above. Copies of the proposed collection of information can be obtained and comments may be forwarded by writing to Administration for Children and Families, Office of Planning, Research, and Evaluation, 330 C Street SW., Washington, DC 20416, Attn: ACF Reports Clearance Officer. Email address: infocollection@acf.hhs.gov. All requests should be identified by the title of the information collection. OMB is required to make a decision concerning 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. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRASUBMISSION@OMB.EoP.GOV, Attn: Desk Officer for the Administration of Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2016–22458 Filed 9–16–16; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request; Child Care and Development Fund Financial Report (ACF–696) for States and Territories OMB No.: 0970–0163. Description: States and Territories use the Financial Report Form ACF–696 to report Child Care and Development Fund (CCDF) expenditures. Authority to collect and report this information is found in section 658G of the Child Care and Development Block Grant Act of 1990, as revised. In addition to the Program Reporting Requirements set forth in 45 CFR part 98, subpart H, the regulations at 45 CFR 98.65(g) and 98.67(c)(1) authorize the Secretary to require financial reports as necessary. The form provides specific data regarding claims and provides a mechanism for States to request Child Care grant awards and to certify the availability of State matching funds. Failure to collect this data would seriously compromise ACF’s ability to monitor Child Care and Development Fund expenditures. This information is also used to estimate outlays and may be used to prepare ACF budget submissions to Congress. The previous information collection requirements related to the American Recovery and Reinvestment Act (ARRA) of 2009, (Pub. L.111–5) have been deleted from this reporting form. Respondents: States and territories. ANNUAL BURDEN ESTIMATES Number of respondents Number of responses per respondent Average burden hours per response Total burden hours ACF–696 .......................................................................................................... mstockstill on DSK3G9T082PROD with NOTICES Instrument 56 4 5 1120 Estimated Total Annual Burden Hours: 1120. Additional Information: Copies of the proposed collection may be obtained by writing to the Administration for Children and Families, Office of VerDate Sep<11>2014 21:47 Sep 16, 2016 Jkt 238001 Planning, Research and Evaluation, 330 C Street SW., Washington, DC 20201. Attention Reports Clearance Officer. All requests should be identified by the title of the information collection. Email address: infocollection@acf.hhs.gov. PO 00000 Frm 00036 Fmt 4703 Sfmt 4703 OMB Comment: OMB is required to make a decision concerning 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 E:\FR\FM\19SEN1.SGM 19SEN1 64162 Federal Register / Vol. 81, No. 181 / Monday, September 19, 2016 / Notices having its full effect if OMB receives it within 30 days of publication. Written comments and recommendations for the proposed information collection should be sent directly to the following: Office of Management and Budget, Paperwork Reduction Project, Email: OIRA_ SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the Administration for Children and Families Robert Sargis, Reports Clearance Officer. [FR Doc. 2016–22449 Filed 9–16–16; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2016–N–2633] International Drug Scheduling; Convention on Psychotropic Substances; Single Convention on Narcotic Drugs; 4-Methylethcathinone and Eleven Other Substances; Request for Comments AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is requesting interested persons to submit comments concerning abuse potential, actual abuse, medical usefulness, trafficking, and impact of scheduling changes on availability for medical use of 12 drug substances. These comments will be considered in preparing a response from the United States to the World Health Organization (WHO) regarding the abuse liability and diversion of these drugs. WHO will use this information to consider whether to recommend that certain international restrictions be placed on these drugs. This notice requesting comments is required by the Controlled Substances Act (the CSA). DATES: Submit either electronic or written comments by October 4, 2016. ADDRESSES: You may submit comments as follows: SUMMARY: mstockstill on DSK3G9T082PROD with NOTICES Electronic Submissions Submit electronic comments in the following way: • Federal eRulemaking Portal: http:// www.regulations.gov. Follow the instructions for submitting comments. Comments submitted electronically, including attachments, to http:// 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 VerDate Sep<11>2014 21:47 Sep 16, 2016 Jkt 238001 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 http://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): Division of Dockets Management (HFA–305), Food and Drug Administration, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. • For written/paper comments submitted to the Division of Dockets Management, 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– 2016–N–2633 for ‘‘International Drug Scheduling; Convention on Psychotropic Substances; Single Convention on Narcotic Drugs; 3,4dichloro-N-[2(dimethylamino)cyclohexyl]-Nmethylbenzamide (U-47700); Butyrfentanyl (Butyrylfentanyl); 4Methylethcathinone (4-MEC); 3Methylmethcathinone (3-methyl-Nmethylcathinone; 3-MMC); Ethylone (3,4-methylenedioxy-N-ethylcathinone; bk-MDEA; MDEC); Pentedrone (aMethylaminovalerophenone); Ethylphenidate (EPH); Methiopropamine (MPA); MDMBCHMICA; 5F–APINACA (5F–AKB48); JWH–073; XLR–11 (5-Fluoro UR-144, 5F-UR-144); Request for Comments.’’ Received comments will be placed in the docket and, except for those submitted as ‘‘Confidential Submissions,’’ publicly viewable at http://www.regulations.gov or at the Division of Dockets Management 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 PO 00000 Frm 00037 Fmt 4703 Sfmt 4703 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 http:// www.regulations.gov. Submit both copies to the Division of Dockets Management. 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: http://www.fda.gov/ regulatoryinformation/dockets/ default.htm. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to http:// 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 Division of Dockets Management, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852. FOR FURTHER INFORMATION CONTACT: James R. Hunter, Center for Drug Evaluation and Research, Controlled Substance Staff, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, Rm. 5150, Silver Spring, MD 20993–0002, 301–796–3156, email: james.hunter@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background The United States is a party to the 1971 Convention on Psychotropic Substances (Psychotropic Convention). Article 2 of the Psychotropic Convention provides that if a party to the convention or WHO has information about a substance, which in its opinion may require international control or change in such control, it shall so notify the Secretary-General of the United Nations (the U.N. Secretary-General) and provide the U.N. Secretary-General E:\FR\FM\19SEN1.SGM 19SEN1

Agencies

[Federal Register Volume 81, Number 181 (Monday, September 19, 2016)]
[Notices]
[Pages 64161-64162]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-22449]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request; Child Care and 
Development Fund Financial Report (ACF-696) for States and Territories

    OMB No.: 0970-0163.
    Description: States and Territories use the Financial Report Form 
ACF-696 to report Child Care and Development Fund (CCDF) expenditures. 
Authority to collect and report this information is found in section 
658G of the Child Care and Development Block Grant Act of 1990, as 
revised. In addition to the Program Reporting Requirements set forth in 
45 CFR part 98, subpart H, the regulations at 45 CFR 98.65(g) and 
98.67(c)(1) authorize the Secretary to require financial reports as 
necessary.
    The form provides specific data regarding claims and provides a 
mechanism for States to request Child Care grant awards and to certify 
the availability of State matching funds. Failure to collect this data 
would seriously compromise ACF's ability to monitor Child Care and 
Development Fund expenditures. This information is also used to 
estimate outlays and may be used to prepare ACF budget submissions to 
Congress.
    The previous information collection requirements related to the 
American Recovery and Reinvestment Act (ARRA) of 2009, (Pub. L.111-5) 
have been deleted from this reporting form.
    Respondents: States and territories.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                  Number of      Average burden
                 Instrument                      Number of      responses per      hours per       Total burden
                                                respondents       respondent        response          hours
----------------------------------------------------------------------------------------------------------------
ACF-696.....................................              56                4                5             1120
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 1120.
    Additional Information: Copies of the proposed collection may be 
obtained by writing to the Administration for Children and Families, 
Office of Planning, Research and Evaluation, 330 C Street SW., 
Washington, DC 20201. Attention Reports Clearance Officer. All requests 
should be identified by the title of the information collection. Email 
address: infocollection@acf.hhs.gov.
    OMB Comment: OMB is required to make a decision concerning 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

[[Page 64162]]

having its full effect if OMB receives it within 30 days of 
publication. Written comments and recommendations for the proposed 
information collection should be sent directly to the following: Office 
of Management and Budget, Paperwork Reduction Project, Email: 
OIRA_SUBMISSION@OMB.EOP.GOV. Attn: Desk Officer for the Administration 
for Children and Families

Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016-22449 Filed 9-16-16; 8:45 am]
 BILLING CODE 4184-01-P