83 FR 57729 - Submission for OMB Review; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 83, Issue 222 (November 16, 2018)
Administration for Children and Families
Federal Register Volume 83, Issue 222 (November 16, 2018)
| Page Range | 57729-57730 | |
| FR Document | 2018-25053 |
[Federal Register Volume 83, Number 222 (Friday, November 16, 2018)] [Notices] [Pages 57729-57730] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-25053] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: National Youth in Transition Database (NYTD) and Youth Outcomes Survey. OMB No.: 0970-0340. Description: The Foster Care Independence Act of 1999 (42 U.S.C. 1305 et seq.) as amended by Public Law 106-169 requires State child welfare agencies to collect and report to the Administration on Children and Families (ACF) data on the characteristics of youth receiving independent living services and information regarding their outcomes. The regulation implementing the National Youth in Transition Database, listed in 45 CFR 1356.80, contains standard data collection and reporting requirements for States to meet the law's requirements. Additionally, the Family First Prevention Services Act of 2017 (H.R. 253) further outlines the expectation of the collection and reporting of data and outcomes regarding youth who are in receipt of independent living services. ACF will use the information collected under the regulation to track independent living services, assess the collective outcomes of youth, and potentially to evaluate State performance with regard to those outcomes consistent with the law's mandate. Respondents: State agencies that administer the John H. Chafee Foster Care Independence Program. The U.S. Virgin Islands have been included in this request as they are expected to begin participating in NYTD data collection efforts during this approval period. Annual Burden Estimates ---------------------------------------------------------------------------------------------------------------- Number of Average burden Instrument Number of responses per hours per Total burden respondents respondent response hours ---------------------------------------------------------------------------------------------------------------- Data file....................................... 53 2 1,430 151,580 Youth Outcomes Survey........................... 16,333 1 .50 8,167 ---------------------------------------------------------------------------------------------------------------- [[Page 57730]] Estimated Total Annual Burden Hours: 155,529. 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: [email protected]. 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: [email protected]. Attn: Desk Officer for the Administration for Children and Families. Robert Sargis, Reports Clearance Officer. [FR Doc. 2018-25053 Filed 11-15-18; 8:45 am] BILLING CODE 4184-01-P
![Federal Register / Vol. 83, No. 222 / Friday, November 16, 2018 / Notices 57729
(SRAE) Program—National Descriptive implementation. ACF seeks approval to effort is to conduct semi-structured
Study collect the following information: interviews, that follow-on the surveys,
OMB NO.: [NEW] with administrators/program directors
Description: The Administration for —Survey for Use with SRAE grantees.
The purpose of this collection effort is in each of the states/organizations that
Children and Families (ACF) proposes a received SRAE grants: The interviews
data collection effort related to the to conduct surveys with
administrators/program directors in will offer long-answer, qualitative
National Evaluation of the Sexual Risk responses to key questions, to better
Avoidance Education (SRAE) Program— each of the states/organizations that
received SRAE grants to better understand what key decisions states/
National Descriptive Study.
The National Descriptive Study (of understand what key decisions states/ organizations made regarding the
the National Evaluation of the SRAE organizations made regarding the design of their SRAE-funded programs
Program) has multiple components. design of their SRAE-funded and why they made those decisions.
This information collection request only programs and why they made those
Respondents: State level
pertains to the Early Implementation decisions.
administrators; Agency administrators;
Study, which will provide an early Interview Guide for Use with SRAE Organization heads; Project directors
catalogue of SRAE programs’ grantees. The purpose of this collection
ANNUAL BURDEN ESTIMATES
Average
Total Annual Number of Annual
burden
Instrument number of number of responses per burden
hours per
respondents respondents respondent hours
response
Survey for SRAE Grantees .................................................. 125 1 1 1 125
Interview Guide for SRAE Grantees .................................... 125 1 1 1 125
Estimated Total Annual Burden collection of information on Families (ACF) data on the
Hours: 250 hours. respondents, including through the use characteristics of youth receiving
In compliance with the requirements of automated collection techniques or independent living services and
of Section 3506(c)(2)(A) of the other forms of information technology. information regarding their outcomes.
Paperwork Reduction Act of 1995, the Consideration will be given to The regulation implementing the
Administration for Children and comments and suggestions submitted National Youth in Transition Database,
Families is soliciting public comment within 60 days of this publication. listed in 45 CFR 1356.80, contains
on the specific aspects of the standard data collection and reporting
information collection described above. Emily Jabbour,
ACF/OPRE Certifying Officer.
requirements for States to meet the law’s
Copies of the proposed collection of requirements. Additionally, the Family
information can be obtained and [FR Doc. 2018–24997 Filed 11–15–18; 8:45 am]
First Prevention Services Act of 2017
comments may be forwarded by writing BILLING CODE 4184–01–P
(H.R. 253) further outlines the
to the Administration for Children and expectation of the collection and
Families, Office of Planning, Research, reporting of data and outcomes
and Evaluation, 330 C Street SW, DEPARTMENT OF HEALTH AND
HUMAN SERVICES regarding youth who are in receipt of
Washington, DC 20201, Attn: OPRE
independent living services. ACF will
Reports Clearance Officer. Email
Administration for Children and use the information collected under the
address: OPREinfocollection@
Families regulation to track independent living
acf.hhs.gov. All requests should be
services, assess the collective outcomes
identified by the title of the information
Submission for OMB Review; of youth, and potentially to evaluate
collection. The Department specifically
Comment Request State performance with regard to those
requests comments on (a) whether the
proposed collection of information is outcomes consistent with the law’s
Title: National Youth in Transition
necessary for the proper performance of mandate.
Database (NYTD) and Youth Outcomes
the functions of the agency, including Survey. Respondents: State agencies that
whether the information shall have OMB No.: 0970–0340. administer the John H. Chafee Foster
practical utility; (b) the accuracy of the Description: The Foster Care Care Independence Program. The U.S.
agency’s estimate of the burden of the Independence Act of 1999 (42 U.S.C. Virgin Islands have been included in
proposed collection of information; (c) 1305 et seq.) as amended by Public Law this request as they are expected to
the quality, utility, and clarity of the 106–169 requires State child welfare begin participating in NYTD data
information to be collected; and (d) agencies to collect and report to the collection efforts during this approval
ways to minimize the burden of the Administration on Children and period.
ANNUAL BURDEN ESTIMATES
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Number of Average
Number of Total burden
Instrument responses per burden hours
respondents hours
respondent per response
Data file ............................................................................................................ 53 2 1,430 151,580
Youth Outcomes Survey .................................................................................. 16,333 1 .50 8,167
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![57730 Federal Register / Vol. 83, No. 222 / Friday, November 16, 2018 / Notices
Estimated Total Annual Burden SUMMARY: The Food and Drug 0738, FDA–2018–M–0792, FDA–2018–
Hours: 155,529. Administration (FDA) is publishing a M–1371, FDA–2018–M–1215, FDA–
Additional Information: Copies of the list of premarket approval applications 2018–M–1237, FDA–2018–M–1372,
proposed collection may be obtained by (PMAs) and humanitarian device FDA–2018–M–1446, FDA–2018–M–
writing to the Administration for exemption applications (HDEs), that 1447, FDA–2018–M–1580, FDA–2018–
Children and Families, Office of have been approved. This list is M–1581, FDA–2018–M–1634, FDA–
Planning, Research and Evaluation, 330 intended to inform the public of the 2018–M–1727, FDA–2018–M–1791,
C Street SW, Washington, DC 20201. availability of safety and effectiveness FDA–2018–M–1753, FDA–2018–M–
Attention Reports Clearance Officer. All summaries of approved PMAs through 1970, FDA–2018–M–2118, FDA–2018–
requests should be identified by the title the internet and the Agency’s Dockets M–2119, FDA–2018–M–2237, FDA–
of the information collection. Email Management Staff. 2018–M–2269, FDA–2018–M–2335,
address: infocollection@acf.hhs.gov. ADDRESSES: You may submit comments FDA–2018–M–2460, FDA–2018–M–
OMB Comment: OMB is required to as follows: 2461, FDA–2018–M–2462, FDA–2018–
make a decision concerning the M–2463, FDA–2018–M–2571, FDA–
collection of information between 30 Electronic Submissions
2018–M–2883, FDA–2018–M–2884,
and 60 days after publication of this Submit electronic comments in the FDA–2018–M–2885, FDA–2018–M–
document in the Federal Register. following way: 2886, FDA–2018–M–2887, FDA–2018–
Therefore, a comment is best assured of • Federal eRulemaking Portal: M–2983, FDA–2018–M–3131, FDA–
having its full effect if OMB receives it https://www.regulations.gov. Follow the 2018–M–3153, FDA–2018–M–3212,
within 30 days of publication. Written instructions for submitting comments. FDA–2018–M–3503, FDA–2018–M–
comments and recommendations for the Comments submitted electronically, 3505, and FDA–2018–M–3548 for
proposed information collection should including attachments, to https:// ‘‘Medical Devices; Availability of Safety
be sent directly to the following: Office www.regulations.gov will be posted to and Effectiveness Summaries for
of Management and Budget Paperwork the docket unchanged. Because your Premarket Approval Applications.’’
Reduction Project Email: OIRA_ comment will be made public, you are Received comments will be placed in
SUBMISSION@OMB.EOP.GOV. Attn: solely responsible for ensuring that your the docket and, except for those
Desk Officer for the Administration for comment does not include any submitted as ‘‘Confidential
Children and Families. confidential information that you or a Submissions,’’ publicly viewable at
third party may not wish to be posted, https://www.regulations.gov or at the
Robert Sargis, such as medical information, your or
Reports Clearance Officer.
Dockets Management Staff between 9
anyone else’s Social Security number, or a.m. and 4 p.m., Monday through
[FR Doc. 2018–25053 Filed 11–15–18; 8:45 am] confidential business information, such Friday.
BILLING CODE 4184–01–P as a manufacturing process. Please note
• Confidential Submissions—To
that if you include your name, contact
submit a comment with confidential
information, or other information that
DEPARTMENT OF HEALTH AND information that you do not wish to be
identifies you in the body of your
HUMAN SERVICES made publicly available, submit your
comments, that information will be
comments only as a written/paper
posted on https://www.regulations.gov.
Food and Drug Administration • If you want to submit a comment submission. You should submit two
with confidential information that you copies total. One copy will include the
[Docket Nos. FDA–2017–M–6970, FDA–
2017–M–6971, FDA–2017–M–6983, FDA– do not wish to be made available to the information you claim to be confidential
2017–M–6984, FDA–2017–M–7004, FDA– public, submit the comment as a with a heading or cover note that states
2018–M–0411, FDA–2018–M–0528, FDA– written/paper submission and in the ‘‘THIS DOCUMENT CONTAINS
2018–M–0620, FDA–2018–M–0736, FDA–
manner detailed (see ‘‘Written/Paper CONFIDENTIAL INFORMATION.’’ The
2018–M–0737, FDA–2018–M–00–0738, FDA–
Submissions’’ and ‘‘Instructions’’). Agency will review this copy, including
2018–M–0792, FDA–2018–M–1371, FDA– the claimed confidential information, in
2018–M–1215, FDA–2018–M–1237, FDA– Written/Paper Submissions its consideration of comments. The
2018–M–1372, FDA–2018–M–1446, FDA–
Submit written/paper submissions as second copy, which will have the
2018–M–1447, FDA–2018–M–1580, FDA–
2018–M–1581, FDA–2018–M–1634, FDA– follows: claimed confidential information
2018–M–1727, FDA–2018–M–1791, FDA– • Mail/Hand Delivery/Courier (for redacted/blacked out, will be available
2018–M–1753, FDA–2018–M–1970, FDA– written/paper submissions): Dockets for public viewing and posted on
2018–M–2118, FDA–2018–M–2119, FDA– Management Staff (HFA–305), Food and https://www.regulations.gov. Submit
2018–M–2237, FDA–2018–M–2269, FDA– Drug Administration, 5630 Fishers both copies to the Dockets Management
2018–M–2335, FDA–2018–M–2460, FDA– Lane, Rm. 1061, Rockville, MD 20852. Staff. If you do not wish your name and
2018–M–2461, FDA–2018–M–2462, FDA– • For written/paper comments contact information to be made publicly
2018–M–2463, FDA–2018–M–2571, FDA– available, you can provide this
2018–M–2883, FDA–2018–M–2884, FDA–
submitted to the Dockets Management
2018–M–2885, FDA–2018–M–2886, FDA– Staff, FDA will post your comment, as information on the cover sheet and not
2018–M–2887, FDA–2018–M–2983, FDA– well as any attachments, except for in the body of your comments and you
2018–M–3131, FDA–2018–M–3153, FDA– information submitted, marked and must identify this information as
2018–M–3212, FDA–2018–M–3503, FDA– identified, as confidential, if submitted ‘‘confidential.’’ Any information marked
2018–M–3505, and FDA–2018–M–3548] as detailed in ‘‘Instructions.’’ as ‘‘confidential’’ will not be disclosed
Instructions: All submissions received except in accordance with 21 CFR 10.20
amozie on DSK3GDR082PROD with NOTICES
Medical Devices; Availability of Safety must include the Docket Nos. FDA– and other applicable disclosure law. For
and Effectiveness Summaries for 2017–M–6970, FDA–2017–M–6971, more information about FDA’s posting
Premarket Approval Applications FDA–2017–M–6983, FDA–2017–M– of comments to public dockets, see 80
AGENCY: Food and Drug Administration, 6984, FDA–2017–M–7004, FDA–2018– FR 56469, September 18, 2015, or access
HHS. M–0411, FDA–2018–M–0528, FDA– the information at: https://www.gpo.gov/
2018–M–0620, FDA–2018–M–0736, fdsys/pkg/FR-2015-09-18/pdf/2015-
ACTION: Notice.
FDA–2018–M–0737, FDA–2018–M–00– 23389.pdf .
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Document Created: 2018-11-16 07:22:22
Document Modified: 2018-11-16 07:22:22
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| FR Citation | 83 FR 57729 |
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