Proposed Information Collection Activity; Comment Request, 21353-21354 [2016-08201]

Download as PDF 21353 Federal Register / Vol. 81, No. 69 / Monday, April 11, 2016 / Notices ANNUAL BURDEN ESTIMATES Total number of respondents Annual number of respondents Number of responses per respondent Average burden hours per response Annual burden hours Instrument Respondent 1—Screening questions for parenting intervention. 2—Screening questions for employment intervention. 3—Consent Materials for Parents of Fathers under 18. Applicant .............. Staff ..................... Applicant .............. Staff ..................... Parent of Applicant. Staff ..................... Applicant .............. Staff ..................... Applicant .............. Staff ..................... Staff ..................... 4,000 36 900 12 500 36 1,333 12 300 4 167 12 1 111 1 75 1 14 0.083 0.083 0.250 0.250 0.167 0.167 111 111 75 75 28 28 6,400 72 2,700 72 72 2,133 24 900 24 24 1 89 1 38 363 0.017 0.017 0.153 0.151 0.008 36 36 138 138 70 Applicant .............. Staff ..................... Applicant .............. Applicant .............. Staff ..................... 450 12 2,842 2,430 240 150 4 947 810 80 1 1,969 1 1 2 0.250 0.0343 0.800 0.667 1.5 38 270 758 540 240 Staff ..................... Applicant .............. Co-parent of Applicant. Applicant .............. Staff ..................... 240 160 80 80 53 27 1 1 1 0.667 2.0 1.0 53 106 27 1,350 36 450 12 5 104 0.117 0.083 263 104 4—B3-specific eligibility data ............. 5—B3-specific enrollment data .......... 6—B3 tracking of attendance in services for program group members. 7—Additional nFORM burden for non-Grantee site. 8 & 9—Baseline surveys ................... 10 & 11—6 month follow-up surveys. 12 & 13—Staff and management semi-structured interviews. 14 & 15—Staff surveys ...................... 16—Participant focus groups ............ 17—Mother Focus Groups ................ 18 & 19—Mobile device surveys ....... 20—Post-session debrief for sites testing parenting intervention. mstockstill on DSK4VPTVN1PROD with NOTICES Estimated Total Annual Burden Hours: 3,245. 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: VerDate Sep<11>2014 18:37 Apr 08, 2016 Jkt 238001 Desk Officer for the Administration for Children and Families. Robert Sargis, ACF Reports Clearance Officer. [FR Doc. 2016–08202 Filed 4–8–16; 8:45 am] BILLING CODE 4184–73–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Title: Personal Responsibility Education Program (PREP) Performance Measures and Adult Preparation Subjects (PMAPS) Studies—Data Collection Related to the Performance Measures Study. OMB No.: New Collection. Description: The Office of Data Analysis, Research, and Evaluation (HHS/ACF/ACYF/ODARE) and the Family and Youth Services Bureau (HHS/ACF/ACYF/FYSB) in the Administration for Children and Families (ACF) propose a data collection activity as part of the PO 00000 Frm 00045 Fmt 4703 Sfmt 4703 Personal Responsibility Education Program (PREP) Performance Measures and Adult Preparation Subjects (PMAPS) Studies. The goals of the PMAPS studies are to collect, analyze, and report on performance measure data for PREP programs and to develop and test Adult Preparation Subjects (APS) conceptual models. The PMAPS studies consist of two components: The ‘‘Performance Measures Study,’’ and the ‘‘Adult Preparation Subjects Study.’’ This notice is specific to data collection activities for the Performance Measures Study only. The Performance Measures Study component includes collection and analysis of performance measure data from State PREP (SPREP), Tribal PREP (TPREP), Competitive PREP (CPREP), and Personal Responsibility Education Innovative Strategies (PREIS) grantees. Data will be used to determine if PREP and PREIS grantees are meeting performance benchmarks related to the program’s mission and priorities. Respondents: Performance measurement data collection instruments will be administered to individuals representing SPREP, TPREP, CPREP, and PREIS grantees, their subawardees, and program participants. E:\FR\FM\11APN1.SGM 11APN1 21354 Federal Register / Vol. 81, No. 69 / Monday, April 11, 2016 / Notices ANNUAL BURDEN ESTIMATES Total number of respondents Instrument Participant Entry Survey ...................................................... Participant Exit Survey ......................................................... Performance reporting system data form—grantees .......... Performance reporting system data form—subawardees ... Estimated Total Annual Burden Hours: 207,926 In compliance with the requirements of Section 3506(c)(2)(A) of the Paperwork Reduction Act of 1995, 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 the Administration for Children and Families, Office of Planning, Research and Evaluation, 330 C Street SW., Washington, DC 20201, Attn: OPRE Reports Clearance Officer. Email address: OPREinfocollection@ acf.hhs.gov. All requests should be identified by the title of the information collection. The Department specifically requests comments on (a) whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information shall have practical utility; (b) the accuracy of the agency’s estimate of the burden of the proposed collection of information; (c) the quality, utility, and clarity of the information to be collected; and (d) ways to minimize the burden of the collection of information on respondents, including through the use of automated collection techniques or other forms of information technology. Consideration will be given to comments and suggestions submitted within 60 days of this publication. Robert Sargis Reports Clearance Officer. 504,279 551,847 951 5,883 DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2012–N–0306] Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Administrative Detention and Banned Medical Devices AGENCY: Food and Drug Administration, HHS. ACTION: BILLING CODE 4184–37–P Notice. The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995. SUMMARY: Fax written comments on the collection of information by May 11, 2016. DATES: To ensure that comments on the information collection are received, OMB recommends that written comments be faxed to the Office of Information and Regulatory Affairs, OMB, Attn: FDA Desk Officer, FAX: 202–395–7285, or emailed to oira_ submission@omb.eop.gov. All comments should be identified with the OMB control number 0910–0114. Also include the FDA docket number found in brackets in the heading of this document. ADDRESSES: FDA PRA Staff, Office of Operations, Food and Drug Administration, 8455 Colesville Rd., COLE–14526, Silver Spring, MD 20993–0002, PRAStaff@ fda.hhs.gov. In compliance with 44 U.S.C. 3507, FDA has submitted the following proposed collection of information to OMB for review and clearance. SUPPLEMENTARY INFORMATION: VerDate Sep<11>2014 18:37 Apr 08, 2016 Jkt 238001 PO 00000 Frm 00046 Fmt 4703 Sfmt 4703 Number of responses per respondent 168,093 183,949 317 1,961 FOR FURTHER INFORMATION CONTACT: [FR Doc. 2016–08201 Filed 4–8–16; 8:45 am] mstockstill on DSK4VPTVN1PROD with NOTICES Annual number of respondents 1 1 2 2 Average burden hours per response .25 .50 30 14 Annual burden hours 42,023 91,975 19,020 54,908 Administrative Detention and Banned Medical Devices—21 CFR 800.55(g)(1) and (g)(2), 800.55(k), 895.21(d), and 895.22; OMB Control Number 0910– 0114—Extension FDA has the statutory authority under section 304(g) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 334(g)) to detain during established inspections devices that are believed to be adulterated or misbranded. Section 800.55 (21 CFR 800.55), on administrative detention, includes among other things, certain reporting requirements and recordkeeping requirements. Under § 800.55(g), an applicant of a detention order must show documentation of ownership if devices are detained at a place other than that of the appellant. Under § 800.55(k), the owner or other responsible person must supply records about how the devices may have become adulterated or misbranded, in addition to records of distribution of the detained devices. These recordkeeping requirements for administrative detentions permit FDA to trace devices for which the detention period expired before a seizure is accomplished or injunctive relief is obtained. FDA also has the statutory authority under section 516 of the FD&C Act (21 U.S.C. 360f) to ban devices that present substantial deception or an unreasonable and substantial risk of illness or injury. Section 895.21 (21 CFR 895.21), on banned devices, contains certain reporting requirements. Section 895.21(d) describes the procedures for banning a device when the Commissioner of Food and Drugs (the Commissioner) decides to initiate such a proceeding. Under 21 CFR 895.22, a manufacturer, distributor, or importer of a device may be required to submit to FDA all relevant and available data and information to enable the Commissioner to determine whether the device presents substantial deception, unreasonable and substantial risk of illness or injury, or unreasonable, direct, and substantial danger to the health of individuals. During the past several years, there has been an average of less than one new administrative detention action per E:\FR\FM\11APN1.SGM 11APN1

Agencies

[Federal Register Volume 81, Number 69 (Monday, April 11, 2016)]
[Notices]
[Pages 21353-21354]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-08201]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Proposed Information Collection Activity; Comment Request

    Title: Personal Responsibility Education Program (PREP) Performance 
Measures and Adult Preparation Subjects (PMAPS) Studies--Data 
Collection Related to the Performance Measures Study.
    OMB No.: New Collection.
    Description: The Office of Data Analysis, Research, and Evaluation 
(HHS/ACF/ACYF/ODARE) and the Family and Youth Services Bureau (HHS/ACF/
ACYF/FYSB) in the Administration for Children and Families (ACF) 
propose a data collection activity as part of the Personal 
Responsibility Education Program (PREP) Performance Measures and Adult 
Preparation Subjects (PMAPS) Studies. The goals of the PMAPS studies 
are to collect, analyze, and report on performance measure data for 
PREP programs and to develop and test Adult Preparation Subjects (APS) 
conceptual models.
    The PMAPS studies consist of two components: The ``Performance 
Measures Study,'' and the ``Adult Preparation Subjects Study.'' This 
notice is specific to data collection activities for the Performance 
Measures Study only. The Performance Measures Study component includes 
collection and analysis of performance measure data from State PREP 
(SPREP), Tribal PREP (TPREP), Competitive PREP (CPREP), and Personal 
Responsibility Education Innovative Strategies (PREIS) grantees. Data 
will be used to determine if PREP and PREIS grantees are meeting 
performance benchmarks related to the program's mission and priorities.
    Respondents: Performance measurement data collection instruments 
will be administered to individuals representing SPREP, TPREP, CPREP, 
and PREIS grantees, their subawardees, and program participants.

[[Page 21354]]



                                             Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
                                                   Annual number     Number of    Average burden
           Instrument              Total number         of         responses per     hours per     Annual burden
                                  of respondents    respondents     respondent       response          hours
----------------------------------------------------------------------------------------------------------------
Participant Entry Survey........         504,279         168,093               1             .25          42,023
Participant Exit Survey.........         551,847         183,949               1             .50          91,975
Performance reporting system                 951             317               2              30          19,020
 data form--grantees............
Performance reporting system               5,883           1,961               2              14          54,908
 data form--subawardees.........
----------------------------------------------------------------------------------------------------------------

    Estimated Total Annual Burden Hours: 207,926
    In compliance with the requirements of Section 3506(c)(2)(A) of the 
Paperwork Reduction Act of 1995, 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 the Administration for Children and Families, Office of 
Planning, Research and Evaluation, 330 C Street SW., Washington, DC 
20201, Attn: OPRE Reports Clearance Officer. Email address: 
OPREinfocollection@acf.hhs.gov. All requests should be identified by 
the title of the information collection.
    The Department specifically requests comments on (a) whether the 
proposed collection of information is necessary for the proper 
performance of the functions of the agency, including whether the 
information shall have practical utility; (b) the accuracy of the 
agency's estimate of the burden of the proposed collection of 
information; (c) the quality, utility, and clarity of the information 
to be collected; and (d) ways to minimize the burden of the collection 
of information on respondents, including through the use of automated 
collection techniques or other forms of information technology. 
Consideration will be given to comments and suggestions submitted 
within 60 days of this publication.

Robert Sargis
Reports Clearance Officer.
[FR Doc. 2016-08201 Filed 4-8-16; 8:45 am]
 BILLING CODE 4184-37-P

This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.