Proposed Information Collection Activity; Comment Request, 41801-41802 [2013-16643]
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Federal Register / Vol. 78, No. 133 / Thursday, July 11, 2013 / Notices
official rules posted on the challenge
site, vetoviolence.challenge.gov. Prior to
entering a submission to the challenge,
contestants must follow the challenge
rules before the end of the submission
period.
Amount of the Prize: One prize
winner for each category, including
General Public View, Student View, and
Violence Prevention Professional View,
will receive an award in the amount of
$500 after the notification of the
winners. A total of $1,500 will be
distributed as awards by the contractor.
Payment of the Prize: Prizes under
this competition will be paid by
electronic funds transfer by Westat
Health Communications as part of their
VetoViolence Facebook contract with
the HHS/CDC Injury Center’s Division
of Violence Prevention.
Basis Upon Which Winners Will be
Selected: Submissions to the challenge
will be assessed by a panel of judges
composed of HHS/CDC Injury Center
teen dating violence subject matter
experts and communications staff and
external injury and violence
professionals in compliance with the
requirements of the America
COMPETES Act. Judges will be named
after the commencement of the
challenge on July 15, 2013. The judging
panel will make decisions based on the
following criteria:
(1) Creativity: Each entry will be
judged on creativity demonstrated in the
delivery of teen dating violence
prevention messages.
(2) Communication of teen dating
violence prevention messages: Each
entry will be judged on the expression
of positive prevention of teen dating
violence messages. The submissions
should not contain real or simulated
acts of violence, profane language,
inappropriate content, or personal or
professional attacks.
(3) Length of Video: Each entry
should be 60 seconds or less.
(4) Video and Audio Quality: Each
entry should be visually focused and
have audible sound quality.
Submissions should not be difficult to
watch because of an unclear image or to
hear because of a poor audio recording.
(5) Fulfilling contest purpose: Each
entry will be judged on its overall
success in meeting the contest goal:
Development of video public service
announcements (PSA) that increase the
understanding (1) that teen dating
violence is a public health problem and
(2) that prevention efforts can stop it
before it starts.
One prize winner for each category—
General Public View, Student View, and
Violence Prevention Professional
View—will receive an award in the
amount of $500 after the notification of
the winners. A total of $1,500 will be
distributed among the three winners.
Additional Information: Finalists and
the contest winners must comply with
all terms and conditions of the official
rules posted on the challenge site,
vetoviolence.challenge.gov, and winning
is contingent upon fulfilling all
requirements herein. The finalists will
be notified by email, telephone, or mail
after the date of the judging.
Contestant information provided
during registration will be used to
respond to contestants in matters
regarding their submission,
announcements of entrants, finalists,
and winners of the contest. Information
is not collected for commercial
marketing. Winners are permitted to cite
that they won this contest.
HHS/CDC reserves the right to cancel,
suspend, and/or modify the contest, or
any part of it, for any reason, at HHS/
CDC’s sole discretion.
More information on teen dating
violence may be found at https://
www.cdc.gov/violenceprevention/
intimatepartnerviolence/
teen_dating_violence.html. More
information on VetoViolence may be
found at https://vetoviolence.cdc.gov/
and https://www.facebook.com/
vetoviolence.
Dated: July 5, 2013.
Tanja Popovic,
Deputy Associate Director for Science,
Centers for Disease Control and Prevention.
[FR Doc. 2013–16619 Filed 7–10–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Evaluation of the Transitional
Living Program (TLP)
OMB No.: 0970–0383
Description: The Runaway and
Homeless Youth Act (RHYA), as
amended by Public Law 106–71 (42
U.S.C. 5701 et seq.), provides for the
Transitional Living Program (TLP), a
residential program lasting up to 18
months designed to prepare older
homeless youth ages 16–21 for a healthy
and self-sufficient adulthood. Section
119 of RHYA requires a study on the
long-term housing outcomes of youth
after exiting the program. In addition to
collecting information on housing
outcomes, the study will also consider
the living, employment, education, and
family situation of the youth before and
after their time in the TLP. This
information will be used to better
understand the most effective practices
in improving long-term outcomes of
youth in an effort to guide program
improvements.
Respondents: (1) Youth ages 16–21
participating in Transitional Living
Programs and (2) the Executive Director
and Program Manager representing TLP
grantees.
ANNUAL BURDEN ESTIMATES
Number of
respondents
emcdonald on DSK67QTVN1PROD with NOTICES
Instrument
Grantee Survey ............................................................................
Youth Baseline Survey ................................................................
Youth 6-Month Follow Up ............................................................
Youth 12-Month Follow Up ..........................................................
Youth 18-Month Follow Up ..........................................................
Estimated Total Annual Burden
Hours: 2,715.
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
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Number of
responses per
respondent
15
1250
1250
1250
1250
1
1
1
1
1
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
PO 00000
Frm 00021
Fmt 4703
Sfmt 4703
Average
burden hours
per response
1
0.75
0.33
0.33
0.75
Total
burden hours
15
937.50
412.50
412.50
937.50
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
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Federal Register / Vol. 78, No. 133 / Thursday, July 11, 2013 / Notices
Families, Office of Planning, Research
and Evaluation, 370 L’Enfant
Promenade SW., Washington, DC 20447,
Attn: ACF Reports Clearance Officer.
Email address: infocollection@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. 2013–16643 Filed 7–10–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2013–N–0115]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Manufactured
Food Regulatory Program Standards
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
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.
DATES: Fax written comments on the
collection of information by August 12,
2013.
ADDRESSES: 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 0910–0601. Also
include the FDA docket number found
in brackets in the heading of this
document.
SUMMARY:
Ila
S. Mizrachi, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
7726, Ila.Mizrachi@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
FOR FURTHER INFORMATION CONTACT:
Manufactured Food Regulatory
Program Standards—(OMB Control
Number 0910–0601)—Extension
In the Federal Register of July 20,
2006 (71 FR 41221), FDA announced the
availability of a draft document entitled
‘‘Manufactured Food Regulatory
Program Standards (MFRPS).’’ These
draft program standards are the
framework that States should use to
design and manage its manufactured
food program. The implementation of
the standards will be negotiated as an
option for payment under the State food
contract. States that are awarded this
option will receive up to $25,000 over
a period of 5 years to fully implement
the program standards. Additionally, 26
States may receive up to $300,000 each
year for a period of 5 years to be in
compliance with the 10 standards.
In the first year of implementing the
program standards, the State program
conducts a baseline self-assessment to
determine if they meet the elements of
each standard. The State program
should use the worksheets and forms
contained herein; however, it can use
alternate forms that are equivalent. The
State program maintains the documents
and verifying records required for each
standard. The information contained in
the documents must be current and fitfor-use. If the State program fails to meet
all program elements and
documentation requirements of a
standard, it develops a strategic plan
which includes the following: (1) The
individual element of documentation
requirement of the standard that was not
met; (2) improvements needed to meet
the program element or documentation
requirement of the standard; and (3)
projected completion dates for each
task.
In the Federal Register of February
19, 2013 (78 FR 11651), FDA published
a 60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Respondent
Number of
respondents
Number of
responses per
respondent
Total annual
responses
Average
burden per
response
Total hours
State Departments of Agriculture or Health ........................
44
1
44
303
13,332
emcdonald on DSK67QTVN1PROD with NOTICES
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
The burden has been calculated to
303 hours per respondent. This burden
was determined by capturing the
average amount of time for each
respondent to assess the current state of
the program and work toward
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implementation of each of the 10
standards contained in MFRPS. The
hours per respondent will remain the
same as implementation to account for
continuing improvement and selfsufficiency in the program.
PO 00000
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Fmt 4703
Sfmt 4703
Dated: July 5, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–16620 Filed 7–10–13; 8:45 am]
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[Federal Register Volume 78, Number 133 (Thursday, July 11, 2013)]
[Notices]
[Pages 41801-41802]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-16643]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Evaluation of the Transitional Living Program (TLP)
OMB No.: 0970-0383
Description: The Runaway and Homeless Youth Act (RHYA), as amended
by Public Law 106-71 (42 U.S.C. 5701 et seq.), provides for the
Transitional Living Program (TLP), a residential program lasting up to
18 months designed to prepare older homeless youth ages 16-21 for a
healthy and self-sufficient adulthood. Section 119 of RHYA requires a
study on the long-term housing outcomes of youth after exiting the
program. In addition to collecting information on housing outcomes, the
study will also consider the living, employment, education, and family
situation of the youth before and after their time in the TLP. This
information will be used to better understand the most effective
practices in improving long-term outcomes of youth in an effort to
guide program improvements.
Respondents: (1) Youth ages 16-21 participating in Transitional
Living Programs and (2) the Executive Director and Program Manager
representing TLP grantees.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Grantee Survey........................ 15 1 1 15
Youth Baseline Survey................. 1250 1 0.75 937.50
Youth 6-Month Follow Up............... 1250 1 0.33 412.50
Youth 12-Month Follow Up.............. 1250 1 0.33 412.50
Youth 18-Month Follow Up.............. 1250 1 0.75 937.50
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 2,715.
In compliance with the requirements of Section 506(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
[[Page 41802]]
Families, Office of Planning, Research and Evaluation, 370 L'Enfant
Promenade SW., Washington, DC 20447, Attn: ACF Reports Clearance
Officer. Email address: infocollection@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. 2013-16643 Filed 7-10-13; 8:45 am]
BILLING CODE 4184-01-P
