82 FR 56030 - Submission for OMB Review; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 82, Issue 226 (November 27, 2017)
Administration for Children and Families
Federal Register Volume 82, Issue 226 (November 27, 2017)
| Page Range | 56030-56031 | |
| FR Document | 2017-25444 |
[Federal Register Volume 82, Number 226 (Monday, November 27, 2017)] [Notices] [Pages 56030-56031] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2017-25444] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request Title: Personal Responsibility Education Program (PREP) Multi- Component Evaluation Extension. OMB No.: 0970-0398. Description: The Family and Youth Services Bureau (FYSB) and the Office of Planning, Research, Evaluation (OPRE) in the Administration for Children and Families (ACF) are requesting an extension without change of a currently approved information collection (OMB No. 0970- 0398). The purpose of the extension is to complete the ongoing follow- up data collection for the Personal Responsibility Education Program (PREP) Multi-Component Evaluation, which was designed to document how PREP programs are designed and implemented in the field, collect performance measure data for PREP programs, and assess the effectiveness of selected PREP-funded programs. The PREP Multi-Component Evaluation contains three components: A Design and Implementation Study, a Performance Analysis Study, and an Impact and In-Depth Implementation Study. Data collection related to the Design and Implementation Study is complete; data collection related to the Performance Analysis Study will be complete in late summer 2017. This notice is specific to data collection activities for the Impact and In-Depth Implementation Study, which is being conducted in four sites. The proposed extension is necessary to complete ongoing follow-up data collection. The resulting data will be used in a rigorous program impact analysis to assess the effectiveness of each program in reducing teen sexual activity and associated risk behaviors. Respondents: Youth participants who agreed to participate in the study upon enrollment in the four impact study sites. Annual Burden Estimates ---------------------------------------------------------------------------------------------------------------- Total/annual Number of Average burden Instrument number of responses per hours per Total/annual respondents respondents response burden hours ---------------------------------------------------------------------------------------------------------------- Second follow-up survey..................... 325 1 .75 244 ---------------------------------------------------------------------------------------------------------------- [[Page 56031]] Estimated Total/Annual Burden Hours: 244. 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, Attn: OPRE 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. Mary Jones, ACF/OPRE Certifying Officer. [FR Doc. 2017-25444 Filed 11-24-17; 8:45 am] BILLING CODE 4184-37-P
![56030 Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices
During the data collection period, assessments performed to examine their partners, and their infants; and to
researchers will follow a subset of 900 developmental delays. help agencies prepare to provide
infants until 2-years of age. A parent of CDC will use study results to guide services to affected children and
each of these infants will answer a recommendations made by both INS families. Participation in this study is
questionnaire at 6, 9, 12, 18, and 24 and CDC to prevent ZIKV infection; to voluntary and there are no costs to
months, as well as have other clinical improve counseling of patients about participants other than their time.
risks to themselves, their pregnancies, The total burden hours are 14,210.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of
Number of burden per
Type of respondents Form name responses per
respondents response
respondent (in hours)
Pregnant Women ............................................ Pregnant Women Eligibility Questionnaire .... 600 1 5/60
Pregnant Women Enrollment Questionnaire 500 1 35/60
Adult Symptoms Questionnaire ..................... 500 15 10/60
Pregnant Women Follow-up Questionnaire ... 500 8 15/60
Infant Symptoms Questionnaire ..................... 2,250 14 10/60
Parent-Child Eligibility Questionnaire ............. 1,000 1 5/60
Parent-Child Enrollment Questionnaire ......... 900 1 20/60
Parent-Child Follow-up Questionnaire ........... 900 4 15/60
Ages and Stages Questionnaire: 2 and 6 2,250 2 15/60
Month Visits.
Ages and Stages Questionnaire: 12 and 24 900 2 15/60
Month Visits.
Bayley Scales of Infant and Toddler Devel- 900 3 30/60
opment.
Strengths and Difficulties Questionnaire ........ 900 1 5/60
Peabody Developmental Motor Scales .......... 900 1 30/60
Parenting Stress Index IV .............................. 900 5 10/60
Center for Epidemiologic Studies Depression 900 5 5/60
Scale.
Test of Nonverbal Intelligence ....................... 900 1 20/60
Male partners .................................................. Male Partner Eligibility Questionnaire ............ 150 1 5/60
Male Enrollment Questionnaire ...................... 125 1 25/60
Adult Symptoms Questionnaire ..................... 125 7 10/60
Leroy A. Richardson, Description: The Family and Youth Performance Analysis Study, and an
Chief, Information Collection Review Office, Services Bureau (FYSB) and the Office Impact and In-Depth Implementation
Office of Scientific Integrity, Office of the of Planning, Research, Evaluation Study. Data collection related to the
Associate Director for Science, Office of the (OPRE) in the Administration for Design and Implementation Study is
Director, Centers for Disease Control and Children and Families (ACF) are complete; data collection related to the
Prevention. requesting an extension without change Performance Analysis Study will be
[FR Doc. 2017–25495 Filed 11–24–17; 8:45 am] of a currently approved information complete in late summer 2017. This
BILLING CODE 4163–18–P collection (OMB No. 0970–0398). The notice is specific to data collection
purpose of the extension is to complete activities for the Impact and In-Depth
the ongoing follow-up data collection Implementation Study, which is being
DEPARTMENT OF HEALTH AND for the Personal Responsibility conducted in four sites. The proposed
HUMAN SERVICES Education Program (PREP) Multi- extension is necessary to complete
Administration for Children and Component Evaluation, which was ongoing follow-up data collection. The
Families designed to document how PREP resulting data will be used in a rigorous
programs are designed and program impact analysis to assess the
Submission for OMB Review; implemented in the field, collect effectiveness of each program in
Comment Request performance measure data for PREP reducing teen sexual activity and
programs, and assess the effectiveness of associated risk behaviors.
Title: Personal Responsibility selected PREP-funded programs. Respondents: Youth participants who
Education Program (PREP) Multi- The PREP Multi-Component agreed to participate in the study upon
Component Evaluation Extension. Evaluation contains three components: enrollment in the four impact study
OMB No.: 0970–0398. A Design and Implementation Study, a sites.
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ANNUAL BURDEN ESTIMATES
Total/annual Number of Average Total/annual
Instrument number of responses per burden hours burden hours
respondents respondents per response
Second follow-up survey ................................................................................. 325 1 .75 244
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![Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices 56031
Estimated Total/Annual Burden Desk Officer for the Administration for been approved by the Office of
Hours: 244. Children and Families. Management and Budget (OMB) under
Additional Information: Copies of the the Paperwork Reduction Act of 1995.
Mary Jones,
proposed collection may be obtained by ACF/OPRE Certifying Officer. FOR FURTHER INFORMATION CONTACT: Ila
writing to the Administration for S. Mizrachi, Office of Operations, Food
[FR Doc. 2017–25444 Filed 11–24–17; 8:45 am]
Children and Families, Office of and Drug Administration, Three White
BILLING CODE 4184–37–P
Planning, Research and Evaluation, 330 Flint North, 10A–12M, 11601
C Street SW., Washington, DC 20201, Landsdown St., North Bethesda, MD
Attn: OPRE Reports Clearance Officer. DEPARTMENT OF HEALTH AND 20852, 301–796–7726, PRAStaff@
All requests should be identified by the HUMAN SERVICES fda.hhs.gov.
title of the information collection. Email SUPPLEMENTARY INFORMATION: The
address: OPREinfocollection@ Food and Drug Administration following is a list of FDA information
acf.hhs.gov. collections recently approved by OMB
[Docket Nos. FDA–2010–N–0601, FDA–
OMB Comment: OMB is required to 2010–N–0598, FDA–2010–N–0600, FDA– under section 3507 of the Paperwork
make a decision concerning the 2007–N–0037, FDA–2010–N–0597, FDA– Reduction Act of 1995 (44 U.S.C. 3507).
collection of information between 30 2011–N–0017, and FDA–2016–N–2496] The OMB control number and
and 60 days after publication of this expiration date of OMB approval for
document in the Federal Register. Agency Information Collection each information collection are shown
Therefore, a comment is best assured of Activities; Announcement of Office of in Table 1. Copies of the supporting
having its full effect if OMB receives it Management and Budget Approvals statements for the information
within 30 days of publication. Written AGENCY: Food and Drug Administration, collections are available on the internet
comments and recommendations for the HHS. at https://www.reginfo.gov/public/do/
proposed information collection should ACTION: Notice. PRAMain. An Agency may not conduct
be sent directly to the following: Office or sponsor, and a person is not required
of Management and Budget, Paperwork SUMMARY: The Food and Drug to respond to, a collection of
Reduction Project, Email: OIRA_ Administration (FDA) is publishing a information unless it displays a
SUBMISSION@OMB.EOP.GOV, Attn: list of information collections that have currently valid OMB control number.
TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB
Date
OMB
Title of collection approval
control No. expires
Current Good Manufacturing Practice for Medicated Feeds ...................................................................... 0910–0152 8/31/2020
Current Good Manufacturing Practice for Type A Medicated Articles ........................................................ 0910–0154 8/31/2020
Animal Drug User Fee Cover Sheet, Form FDA 3546 ............................................................................... 0910–0539 8/31/2020
Animal Drug User Fee Waivers and Reductions ........................................................................................ 0910–0540 8/31/2020
Index of Legally Marketed Unappropriated New Animal Drugs for Minor Species .................................... 0910–0620 8/31/2020
Voluntary National Retail Food Regulatory Program Standards ................................................................ 0910–0621 8/31/2020
Impact Trade Auxiliary Communication System ......................................................................................... 0910–0842 8/31/2020
Dated: November 20, 2017. comment on the proposed collection of at the end of January 26, 2018.
Leslie Kux, certain information by the Agency. Comments received by mail/hand
Associate Commissioner for Policy. Under the Paperwork Reduction Act of delivery/courier (for written/paper
[FR Doc. 2017–25452 Filed 11–24–17; 8:45 am] 1995 (PRA), Federal Agencies are submissions) will be considered timely
BILLING CODE 4164–01–P
required to publish notice in the if they are postmarked or the delivery
Federal Register concerning each service acceptance receipt is on or
proposed collection of information, before that date.
DEPARTMENT OF HEALTH AND including each proposed extension of an
Electronic Submissions
HUMAN SERVICES existing collection of information, and
to allow 60 days for public comment in Submit electronic comments in the
Food and Drug Administration response to the notice. This notice following way:
solicits comments on export certificates • Federal eRulemaking Portal:
[Docket No. FDA–2010–N–0161] https://www.regulations.gov. Follow the
for the export of FDA-regulated
products. instructions for submitting comments.
Agency Information Collection
Comments submitted electronically,
Activities; Proposed Collection; DATES: Submit either electronic or including attachments, to https://
Comment Request; Export of Food and written comments on the collection of www.regulations.gov will be posted to
Drug Administration-Regulated information by January 26, 2018.
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the docket unchanged. Because your
Products: Export Certificates
ADDRESSES: You may submit comments comment will be made public, you are
AGENCY: Food and Drug Administration, as follows. Please note that late, solely responsible for ensuring that your
HHS. untimely filed comments will not be comment does not include any
ACTION: Notice. considered. Electronic comments must confidential information that you or a
be submitted on or before January 26, third party may not wish to be posted,
SUMMARY: The Food and Drug 2018. The https://www.regulations.gov such as medical information, your or
Administration (FDA or Agency) is electronic filing system will accept anyone else’s Social Security number, or
announcing an opportunity for public comments until midnight Eastern Time confidential business information, such
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Document Created: 2017-11-25 01:08:51
Document Modified: 2017-11-25 01:08:51
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
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| Section | Notices | |
| FR Citation | 82 FR 56030 |
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