81 FR 21353 - Proposed Information Collection Activity; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 81, Issue 69 (April 11, 2016)
Administration for Children and Families
Federal Register Volume 81, Issue 69 (April 11, 2016)
| Page Range | 21353-21354 | |
| FR Document | 2016-08201 |
[Federal Register Volume 81, Number 69 (Monday, April 11, 2016)] [Notices] [Pages 21353-21354] From the Federal Register Online [www.thefederalregister.org] [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: [email protected]. 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
![Federal Register / Vol. 81, No. 69 / Monday, April 11, 2016 / Notices 21353
ANNUAL BURDEN ESTIMATES
Annual Number of Average
Total number Annual burden
Instrument Respondent number of responses per burden hours
of respondents hours
respondents respondent per response
1—Screening questions for parenting Applicant .............. 4,000 1,333 1 0.083 111
intervention. Staff ..................... 36 12 111 0.083 111
2—Screening questions for employ- Applicant .............. 900 300 1 0.250 75
ment intervention. Staff ..................... 12 4 75 0.250 75
3—Consent Materials for Parents of Parent of Appli- 500 167 1 0.167 28
Fathers under 18. cant. 36 12 14 0.167 28
Staff .....................
4—B3-specific eligibility data ............. Applicant .............. 6,400 2,133 1 0.017 36
Staff ..................... 72 24 89 0.017 36
5—B3-specific enrollment data .......... Applicant .............. 2,700 900 1 0.153 138
Staff ..................... 72 24 38 0.151 138
6—B3 tracking of attendance in serv- Staff ..................... 72 24 363 0.008 70
ices for program group members.
7—Additional nFORM burden for Applicant .............. 450 150 1 0.250 38
non-Grantee site. Staff ..................... 12 4 1,969 0.0343 270
8 & 9—Baseline surveys ................... Applicant .............. 2,842 947 1 0.800 758
10 & 11—6 month follow-up surveys. Applicant .............. 2,430 810 1 0.667 540
12 & 13—Staff and management Staff ..................... 240 80 2 1.5 240
semi-structured interviews.
14 & 15—Staff surveys ...................... Staff ..................... 240 80 1 0.667 53
16—Participant focus groups ............ Applicant .............. 160 53 1 2.0 106
17—Mother Focus Groups ................ Co-parent of Ap- 80 27 1 1.0 27
plicant.
18 & 19—Mobile device surveys ....... Applicant .............. 1,350 450 5 0.117 263
20—Post-session debrief for sites Staff ..................... 36 12 104 0.083 104
testing parenting intervention.
Estimated Total Annual Burden Desk Officer for the Administration for Personal Responsibility Education
Hours: 3,245. Children and Families. Program (PREP) Performance Measures
Additional Information: Copies of the and Adult Preparation Subjects
Robert Sargis,
proposed collection may be obtained by (PMAPS) Studies. The goals of the
ACF Reports Clearance Officer. PMAPS studies are to collect, analyze,
writing to the Administration for [FR Doc. 2016–08202 Filed 4–8–16; 8:45 am] and report on performance measure data
Children and Families, Office of BILLING CODE 4184–73–P for PREP programs and to develop and
Planning, Research and Evaluation, 330
test Adult Preparation Subjects (APS)
C Street SW., Washington, DC 20201, conceptual models.
Attn: OPRE Reports Clearance Officer. DEPARTMENT OF HEALTH AND The PMAPS studies consist of two
All requests should be identified by the HUMAN SERVICES components: The ‘‘Performance
title of the information collection. Email Measures Study,’’ and the ‘‘Adult
address: OPREinfocollection@ Administration for Children and
Families Preparation Subjects Study.’’ This
acf.hhs.gov. notice is specific to data collection
OMB Comment: OMB is required to Proposed Information Collection activities for the Performance Measures
make a decision concerning the Activity; Comment Request Study only. The Performance Measures
collection of information between 30 Study component includes collection
and 60 days after publication of this Title: Personal Responsibility and analysis of performance measure
document in the Federal Register. Education Program (PREP) Performance data from State PREP (SPREP), Tribal
Therefore, a comment is best assured of Measures and Adult Preparation PREP (TPREP), Competitive PREP
having its full effect if OMB receives it Subjects (PMAPS) Studies—Data (CPREP), and Personal Responsibility
Collection Related to the Performance Education Innovative Strategies (PREIS)
within 30 days of publication. Written
Measures Study. grantees. Data will be used to determine
comments and recommendations for the
OMB No.: New Collection. if PREP and PREIS grantees are meeting
proposed information collection should
Description: The Office of Data performance benchmarks related to the
be sent directly to the following: Office
Analysis, Research, and Evaluation program’s mission and priorities.
of Management and Budget, Paperwork
(HHS/ACF/ACYF/ODARE) and the Respondents: Performance
Reduction Project, Email: OIRA_ Family and Youth Services Bureau measurement data collection
SUBMISSION@OMB.EOP.GOV, Attn: (HHS/ACF/ACYF/FYSB) in the instruments will be administered to
Administration for Children and individuals representing SPREP, TPREP,
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Families (ACF) propose a data CPREP, and PREIS grantees, their
collection activity as part of the subawardees, and program participants.
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![21354 Federal Register / Vol. 81, No. 69 / Monday, April 11, 2016 / Notices
ANNUAL BURDEN ESTIMATES
Annual Number of Average
Total number Annual burden
Instrument number of responses per burden hours
of respondents hours
respondents respondent per response
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 data form—grantees .......... 951 317 2 30 19,020
Performance reporting system data form—subawardees ... 5,883 1,961 2 14 54,908
Estimated Total Annual Burden DEPARTMENT OF HEALTH AND Administrative Detention and Banned
Hours: 207,926 HUMAN SERVICES Medical Devices—21 CFR 800.55(g)(1)
In compliance with the requirements and (g)(2), 800.55(k), 895.21(d), and
of Section 3506(c)(2)(A) of the Food and Drug Administration 895.22; OMB Control Number 0910–
0114—Extension
Paperwork Reduction Act of 1995, the
Administration for Children and [Docket No. FDA–2012–N–0306] FDA has the statutory authority under
Families is soliciting public comment section 304(g) of the Federal Food, Drug,
on the specific aspects of the Agency Information Collection and Cosmetic Act (the FD&C Act) (21
information collection described above. Activities; Submission for Office of U.S.C. 334(g)) to detain during
Copies of the proposed collection of Management and Budget Review; established inspections devices that are
information can be obtained and Comment Request; Administrative believed to be adulterated or
Detention and Banned Medical Devices misbranded. Section 800.55 (21 CFR
comments may be forwarded by writing
800.55), on administrative detention,
to the Administration for Children and includes among other things, certain
AGENCY: Food and Drug Administration,
Families, Office of Planning, Research reporting requirements and
HHS.
and Evaluation, 330 C Street SW., recordkeeping requirements. Under
Washington, DC 20201, Attn: OPRE ACTION: Notice. § 800.55(g), an applicant of a detention
Reports Clearance Officer. Email order must show documentation of
address: OPREinfocollection@ SUMMARY: The Food and Drug ownership if devices are detained at a
acf.hhs.gov. All requests should be Administration (FDA) is announcing place other than that of the appellant.
identified by the title of the information that a proposed collection of Under § 800.55(k), the owner or other
collection. information has been submitted to the responsible person must supply records
The Department specifically requests Office of Management and Budget about how the devices may have
comments on (a) whether the proposed (OMB) for review and clearance under become adulterated or misbranded, in
collection of information is necessary the Paperwork Reduction Act of 1995. addition to records of distribution of the
for the proper performance of the detained devices. These recordkeeping
DATES: Fax written comments on the requirements for administrative
functions of the agency, including collection of information by May 11, detentions permit FDA to trace devices
whether the information shall have 2016. for which the detention period expired
practical utility; (b) the accuracy of the before a seizure is accomplished or
agency’s estimate of the burden of the ADDRESSES: To ensure that comments on
injunctive relief is obtained.
proposed collection of information; (c) the information collection are received,
FDA also has the statutory authority
the quality, utility, and clarity of the OMB recommends that written under section 516 of the FD&C Act (21
information to be collected; and (d) comments be faxed to the Office of U.S.C. 360f) to ban devices that present
ways to minimize the burden of the Information and Regulatory Affairs, substantial deception or an
collection of information on OMB, Attn: FDA Desk Officer, FAX: unreasonable and substantial risk of
respondents, including through the use 202–395–7285, or emailed to oira_ illness or injury. Section 895.21 (21 CFR
of automated collection techniques or submission@omb.eop.gov. All 895.21), on banned devices, contains
other forms of information technology. comments should be identified with the certain reporting requirements. Section
Consideration will be given to OMB control number 0910–0114. Also 895.21(d) describes the procedures for
comments and suggestions submitted include the FDA docket number found banning a device when the
within 60 days of this publication. in brackets in the heading of this Commissioner of Food and Drugs (the
document. Commissioner) decides to initiate such
Robert Sargis a proceeding. Under 21 CFR 895.22, a
Reports Clearance Officer. FOR FURTHER INFORMATION CONTACT: FDA manufacturer, distributor, or importer of
[FR Doc. 2016–08201 Filed 4–8–16; 8:45 am] PRA Staff, Office of Operations, Food a device may be required to submit to
BILLING CODE 4184–37–P
and Drug Administration, 8455 FDA all relevant and available data and
Colesville Rd., COLE–14526, Silver information to enable the Commissioner
Spring, MD 20993–0002, PRAStaff@ to determine whether the device
mstockstill on DSK4VPTVN1PROD with NOTICES
fda.hhs.gov. presents substantial deception,
unreasonable and substantial risk of
SUPPLEMENTARY INFORMATION: In illness or injury, or unreasonable, direct,
compliance with 44 U.S.C. 3507, FDA and substantial danger to the health of
has submitted the following proposed individuals.
collection of information to OMB for During the past several years, there
review and clearance. has been an average of less than one
new administrative detention action per
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Document Created: 2016-04-09 00:11:04
Document Modified: 2016-04-09 00:11:04
| 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 | 81 FR 21353 |
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