Submission for OMB Review; Comment Request, 57758-57759 [2017-26353]

Download as PDF 57758 Federal Register / Vol. 82, No. 234 / Thursday, December 7, 2017 / Notices ESTIMATED ANNUALIZED BURDEN HOURS—Continued Number of respondents Type of respondents Form name Treatment facility staff ..................................... Client Questionnaire Baseline ........................ Client Questionnaire 12-Month Follow-up ..... Client Questionnaire 24-Month Follow-up ..... Client Focus Groups ...................................... Staff Focus Groups ........................................ Leroy A. Richardson, Chief, Information Collection Review Office, Office of Scientific Integrity, Office of the Associate Director for Science, Office of the Director, Centers for Disease Control and Prevention. [FR Doc. 2017–26399 Filed 12–6–17; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket Number CDC–2017–0104, NIOSH– 304] Draft—National Occupational Research Agenda for Traumatic Injury Prevention National Institute for Occupational Safety and Health (NIOSH) of the Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Request for comment. AGENCY: The National Institute for Occupational Safety and Health of the Centers for Disease Control and Prevention announces the availability of a draft NORA Agenda entitled National Occupational Research Agenda for Traumatic Injury Prevention for public comment. To view the notice and related materials, visit https:// www.regulations.gov. and enter CDC– 2017–0104 in the search field and click ‘‘Search.’’ SUMMARY: sradovich on DSK3GMQ082PROD with NOTICES Table of Contents • • • • • Dates Addresses For Further Information Contact Supplementary Information Background Electronic or written comments must be received by February 5, 2018. ADDRESSES: You may submit comments, identified by CDC–2017–0104 and docket number NIOSH–304, by any of the following methods: DATES: VerDate Sep<11>2014 18:50 Dec 06, 2017 Jkt 244001 • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. • Mail: National Institute for Occupational Safety and Health, NIOSH Docket Office, 1090 Tusculum Avenue, MS C–34, Cincinnati, Ohio 45226–1998. Instructions: All submissions received in response to this notice must include the agency name and docket number [CDC–2017–0104; NIOSH–304]. All relevant comments received will be posted without change to https:// www.regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to https://www.regulations.gov. All information received in response to this notice will also be available for public examination and copying at the NIOSH Docket Office, 1150 Tusculum Avenue, Room 155, Cincinnati, OH 45226–1998. FOR FURTHER INFORMATION CONTACT: Emily Novicki (NORACoordinator@ cdc.gov), National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention, Mailstop E–20, 1600 Clifton Road NE., Atlanta, GA 30329, phone (404) 498– 2581 (not a toll free number). SUPPLEMENTARY INFORMATION: The National Occupational Research Agenda (NORA) is a partnership program created to stimulate innovative research and improved workplace practices. The national agenda is developed and implemented through the NORA sector and cross-sector councils. Each council develops and maintains an agenda for its sector or cross-sector. Background: The National Occupational Research Agenda for Traumatic Injury Prevention (the Agenda) is intended to identify the research, information, and actions most urgently needed to prevent occupational traumatic injuries. The National Occupational Research Agenda for Traumatic Injury Prevention provides a vehicle for industry stakeholders to describe the most relevant issues, gaps, and safety and health needs for the cross-sector. Each NORA research agenda is meant to guide or promote PO 00000 Frm 00056 Fmt 4703 Sfmt 4703 Number of responses per respondent 1,187 930 744 27 27 Average burden per response (in hours) 1 1 1 1 1 52/60 45/60 45/60 90/60 90/60 high priority research efforts on a national level, conducted by various entities, including government, higher education, and the private sector. This is the first Traumatic Injury Prevention Agenda, developed for the third decade of NORA (2016–2026). The Agenda was developed considering information about injuries, the state of the science, and the probability that new information and approaches will make a difference. As the steward of the NORA process, NIOSH invites comments on the draft National Occupational Research Agenda for Traumatic Injury Prevention. Comments expressing support or with specific recommendations to improve the Agenda are requested. A copy of the draft Agenda is available at https:// www.regulations.gov (search Docket Number CDC–2017–0104). Frank Hearl, Chief of Staff, National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. [FR Doc. 2017–26359 Filed 12–6–17; 8:45 am] BILLING CODE 4163–19–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Annual Statistical Report on Children in Foster Homes and Children in Families Receiving Payment in Excess of the Poverty Income Level from a State Program Funded under Part A of Title IV of the Social Security Act. OMB No.: 0970–0004. Description: The Department of Health and Human Services is required to collect these data under section 1124 of Title I of the Elementary and Secondary Education Act of 1965, as amended by Public Law 114–95. The data are used by the U.S. Department of Education for allocation of funds for programs to aid disadvantaged E:\FR\FM\07DEN1.SGM 07DEN1 57759 Federal Register / Vol. 82, No. 234 / Thursday, December 7, 2017 / Notices elementary and secondary students. Respondents include various components of State Human Service agencies. Respondents: The 52 respondents include the 50 States, the District of Columbia, and Puerto Rico. ANNUAL BURDEN ESTIMATES Number of respondents Instrument Annual Statistical Report on Children in Foster Homes and Children Receiving Payments in Excess of the Poverty Level From a State Program Funded Under Part A of Title IV of the Social Security Act ........................ Estimated Total Annual Burden Hours: 13,746.20. 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 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. Food and Drug Administration [Docket No. FDA–2017–N–6476] sradovich on DSK3GMQ082PROD with NOTICES Pediatric Rare Diseases—A Collaborative Approach for Drug Development Using Gaucher Disease as a Model; Draft Guidance for Industry; Availability Food and Drug Administration, HHS. Notice of availability. The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance for industry entitled ‘‘Pediatric SUMMARY: VerDate Sep<11>2014 18:50 Dec 06, 2017 Submit either electronic or written comments on the draft guidance by February 5, 2018 to ensure that the Agency considers your comment on this draft guidance before it begins work on the final version of the guidance. DATES: Electronic Submissions DEPARTMENT OF HEALTH AND HUMAN SERVICES ACTION: Rare Diseases—A Collaborative Approach for Drug Development Using Gaucher Disease as a Model.’’ This draft guidance focuses on drug development for pediatric patients with Gaucher disease. In particular, it proposes for consideration a novel approach to improve the efficiency of drug development in pediatric rare diseases using Gaucher disease as an example. The emergence of concomitant trials for multiple investigational drug products for the treatment of rare diseases can pose significant challenges to effective drug development, because there are limited numbers of patients for any given rare condition worldwide. This approach discusses the feasibility of the development of multiple drug products in a time-efficient manner while minimizing the number of patients necessary to be treated with placebo. You may submit comments on any guidance at any time as follows: BILLING CODE 4184–01–P AGENCY: 52 ADDRESSES: [FR Doc. 2017–26353 Filed 12–6–17; 8:45 am] Jkt 244001 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 PO 00000 Frm 00057 Fmt 4703 Sfmt 4703 Number of responses per respondent 1 Average burden hours per response 264.35 Total burden hours 13,746.20 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– 2017–N–6476 for ‘‘Pediatric Rare Diseases—A Collaborative Approach for Drug Development Using Gaucher Disease as a Model; Draft Guidance for Industry; Availability’’. 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 office 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 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 E:\FR\FM\07DEN1.SGM 07DEN1

Agencies

[Federal Register Volume 82, Number 234 (Thursday, December 7, 2017)]
[Notices]
[Pages 57758-57759]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-26353]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for OMB Review; Comment Request

    Title: Annual Statistical Report on Children in Foster Homes and 
Children in Families Receiving Payment in Excess of the Poverty Income 
Level from a State Program Funded under Part A of Title IV of the 
Social Security Act.
    OMB No.: 0970-0004.
    Description: The Department of Health and Human Services is 
required to collect these data under section 1124 of Title I of the 
Elementary and Secondary Education Act of 1965, as amended by Public 
Law 114-95. The data are used by the U.S. Department of Education for 
allocation of funds for programs to aid disadvantaged

[[Page 57759]]

elementary and secondary students. Respondents include various 
components of State Human Service agencies.
    Respondents: The 52 respondents include the 50 States, the District 
of Columbia, and Puerto Rico.

                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                                     Number of    Average burden
                   Instrument                        Number of     responses per     hours per     Total burden
                                                    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Annual Statistical Report on Children in Foster               52               1          264.35       13,746.20
 Homes and Children Receiving Payments in Excess
 of the Poverty Level From a State Program
 Funded Under Part A of Title IV of the Social
 Security Act...................................
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 13,746.20.
    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 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. 2017-26353 Filed 12-6-17; 8:45 am]
 BILLING CODE 4184-01-P