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