Submission for OMB Review; Comment Request, 56030-56031 [2017-25444]

Download as PDF 56030 Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices During the data collection period, researchers will follow a subset of 900 infants until 2-years of age. A parent of each of these infants will answer a questionnaire at 6, 9, 12, 18, and 24 months, as well as have other clinical their partners, and their infants; and to help agencies prepare to provide services to affected children and families. Participation in this study is voluntary and there are no costs to participants other than their time. The total burden hours are 14,210. assessments performed to examine developmental delays. CDC will use study results to guide recommendations made by both INS and CDC to prevent ZIKV infection; to improve counseling of patients about risks to themselves, their pregnancies, ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Type of respondents Form name Pregnant Women ............................................ Pregnant Women Eligibility Questionnaire .... Pregnant Women Enrollment Questionnaire Adult Symptoms Questionnaire ..................... Pregnant Women Follow-up Questionnaire ... Infant Symptoms Questionnaire ..................... Parent-Child Eligibility Questionnaire ............. Parent-Child Enrollment Questionnaire ......... Parent-Child Follow-up Questionnaire ........... Ages and Stages Questionnaire: 2 and 6 Month Visits. Ages and Stages Questionnaire: 12 and 24 Month Visits. Bayley Scales of Infant and Toddler Development. Strengths and Difficulties Questionnaire ........ Peabody Developmental Motor Scales .......... Parenting Stress Index IV .............................. Center for Epidemiologic Studies Depression Scale. Test of Nonverbal Intelligence ....................... Male Partner Eligibility Questionnaire ............ Male Enrollment Questionnaire ...................... Adult Symptoms Questionnaire ..................... Male partners .................................................. 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. 2017–25495 Filed 11–24–17; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for OMB Review; Comment Request asabaliauskas on DSKBBXCHB2PROD with NOTICES Title: Personal Responsibility Education Program (PREP) MultiComponent 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) MultiComponent 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 Number of responses per respondent Average burden per response (in hours) 600 500 500 500 2,250 1,000 900 900 2,250 1 1 15 8 14 1 1 4 2 5/60 35/60 10/60 15/60 10/60 5/60 20/60 15/60 15/60 900 2 15/60 900 3 30/60 900 900 900 900 1 1 5 5 5/60 30/60 10/60 5/60 900 150 125 125 1 1 1 7 20/60 5/60 25/60 10/60 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 Instrument Total/annual number of respondents Number of responses per respondents Average burden hours per response Total/annual burden hours Second follow-up survey ................................................................................. 325 1 .75 244 VerDate Sep<11>2014 16:59 Nov 24, 2017 Jkt 244001 PO 00000 Frm 00046 Fmt 4703 Sfmt 4703 E:\FR\FM\27NON1.SGM 27NON1 56031 Federal Register / Vol. 82, No. 226 / Monday, November 27, 2017 / Notices 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: OPREinfocollection@ 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. Mary Jones, ACF/OPRE Certifying Officer. [FR Doc. 2017–25444 Filed 11–24–17; 8:45 am] BILLING CODE 4184–37–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket Nos. FDA–2010–N–0601, FDA– 2010–N–0598, FDA–2010–N–0600, FDA– 2007–N–0037, FDA–2010–N–0597, FDA– 2011–N–0017, and FDA–2016–N–2496] Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA) is publishing a list of information collections that have SUMMARY: been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995. FOR FURTHER INFORMATION CONTACT: Ila S. Mizrachi, Office of Operations, Food and Drug Administration, Three White Flint North, 10A–12M, 11601 Landsdown St., North Bethesda, MD 20852, 301–796–7726, PRAStaff@ fda.hhs.gov. The following is a list of FDA information collections recently approved by OMB under section 3507 of the Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control number and expiration date of OMB approval for each information collection are shown in Table 1. Copies of the supporting statements for the information collections are available on the internet at https://www.reginfo.gov/public/do/ PRAMain. An Agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB control number. SUPPLEMENTARY INFORMATION: TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB OMB control No. Title of collection Current Good Manufacturing Practice for Medicated Feeds ...................................................................... Current Good Manufacturing Practice for Type A Medicated Articles ........................................................ Animal Drug User Fee Cover Sheet, Form FDA 3546 ............................................................................... Animal Drug User Fee Waivers and Reductions ........................................................................................ Index of Legally Marketed Unappropriated New Animal Drugs for Minor Species .................................... Voluntary National Retail Food Regulatory Program Standards ................................................................ Impact Trade Auxiliary Communication System ......................................................................................... Dated: November 20, 2017. Leslie Kux, Associate Commissioner for Policy. [FR Doc. 2017–25452 Filed 11–24–17; 8:45 am] BILLING CODE 4164–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration asabaliauskas on DSKBBXCHB2PROD with NOTICES [Docket No. FDA–2010–N–0161] Agency Information Collection Activities; Proposed Collection; Comment Request; Export of Food and Drug Administration-Regulated Products: Export Certificates AGENCY: Food and Drug Administration, HHS. ACTION: Notice. The Food and Drug Administration (FDA or Agency) is announcing an opportunity for public SUMMARY: VerDate Sep<11>2014 16:59 Nov 24, 2017 Jkt 244001 comment on the proposed collection of certain information by the Agency. Under the Paperwork Reduction Act of 1995 (PRA), Federal Agencies are required to publish notice in the Federal Register concerning each proposed collection of information, including each proposed extension of an existing collection of information, and to allow 60 days for public comment in response to the notice. This notice solicits comments on export certificates for the export of FDA-regulated products. Submit either electronic or written comments on the collection of information by January 26, 2018. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. Electronic comments must be submitted on or before January 26, 2018. The https://www.regulations.gov electronic filing system will accept comments until midnight Eastern Time DATES: PO 00000 Frm 00047 Fmt 4703 Sfmt 4703 0910–0152 0910–0154 0910–0539 0910–0540 0910–0620 0910–0621 0910–0842 Date approval expires 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 8/31/2020 at the end of January 26, 2018. 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. 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:// 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 E:\FR\FM\27NON1.SGM 27NON1

Agencies

[Federal Register Volume 82, Number 226 (Monday, November 27, 2017)]
[Notices]
[Pages 56030-56031]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-25444]


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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: OPREinfocollection@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.

Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2017-25444 Filed 11-24-17; 8:45 am]
 BILLING CODE 4184-37-P