Att. B_60dy FRN

Federal Register / Vol. 80, No. 216 / Monday, November 9, 2015 / Notices
122 and 403, is being published in the
Federal Register:

Written comments should be
submitted on or before December 9,
2015. If you anticipate that you will be
submitting comments, but find it
difficult to do so within the period of
time allowed by this notice, you should
advise the contacts below as soon as
possible.

DATES:

Part 123—EPA Administered Permit
Programs: The National Pollutant Discharge
Elimination System; and
Part 403—General Pretreatment
Regulations For Existing And New Sources
Of Pollution.

ME DEP was notified of EPA’s
determination to approve its application
with respect to the authorized programs
listed above.
Matthew Leopard,
Director, Office of Information Collection.
[FR Doc. 2015–28366 Filed 11–6–15; 8:45 am]
BILLING CODE 6560–50–P

Direct all PRA comments to
Nicholas A. Fraser, OMB, via email
[email protected]; and
to Nicole Ongele, FCC, via email PRA@
fcc.gov and to [email protected].
Include in the comments the OMB
control number as shown in the
‘‘Supplementary Information’’ section
below.

ADDRESSES:

For
additional information or copies of the
information collection, contact Nicole
Ongele at (202) 418–2991.
To view a copy of this information
collection request (ICR) submitted to
OMB: (1) Go to the Web page ,
(2) look for the section of the Web page
called ‘‘Currently Under Review,’’ (3)
click on the downward-pointing arrow
in the ‘‘Select Agency’’ box below the
‘‘Currently Under Review’’ heading, (4)
select ‘‘Federal Communications
Commission’’ from the list of agencies
presented in the ‘‘Select Agency’’ box,
(5) click the ‘‘Submit’’ button to the
right of the ‘‘Select Agency’’ box, (6)
when the list of FCC ICRs currently
under review appears, look for the OMB
control number of this ICR and then
click on the ICR Reference Number. A
copy of the FCC submission to OMB
will be displayed.
SUPPLEMENTARY INFORMATION:
OMB Control Number: 3060-xxxx.
Title: Direct Access to Numbers Order
FCC 15–70 Conditions.
Form Number: N/A.
Type of Review: New Collection.
Respondents: Business or other forprofit.
Number of Respondents and
Responses: 13 respondents; 13
responses.
Estimated Time per Response: 120
hours.
Frequency of Response: One-time
application, on-going and bi-annual
reporting requirements.
Obligation To Respond: Voluntary.
Statutory Authority for this information
collection is contained in 47 U.S.C.
251(e)(1).
Total Annual Burden: 1,560 hours.
Total Annual Costs: No Cost.
Privacy Act Impact Assessment: No
impact(s).
Nature and Extent of Confidentiality:
If respondents submit information
which respondents believe is
FOR FURTHER INFORMATION CONTACT:

FEDERAL COMMUNICATIONS
COMMISSION
[3060-xxxx]

Information Collection Being
Submitted for Review and Approval to
the Office of Management and Budget
Federal Communications
Commission.
ACTION: Notice and request for
comments.
AGENCY:

As part of its continuing effort
to reduce paperwork burdens, and as
required by the Paperwork Reduction
Act (PRA) of 1995 (44 U.S.C. 3501–
3520), the Federal Communications
Commission (FCC or Commission)
invites the general public and other
Federal agencies to take this
opportunity to comment on the
following information collections.
Comments are requested concerning:
whether the proposed collection of
information is necessary for the proper
performance of the functions of the
Commission, including whether the
information shall have practical utility;
the accuracy of the Commission’s
burden estimate; ways to enhance the
quality, utility, and clarity of the
information collected; ways to minimize
the burden of the collection of
information on the respondents,
including the use of automated
collection techniques or other forms of
information technology; and ways to
further reduce the information
collection burden on small business
concerns with fewer than 25 employees.
The FCC may not conduct or sponsor a
collection of information unless it
displays a currently valid OMB control
number. No person shall be subject to
any penalty for failing to comply with
a collection of information subject to the
PRA that does not display a valid OMB
control number.

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SUMMARY:

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confidential, respondents may request
confidential treatment of such
information pursuant to section 0.459 of
the Commission’s rules, 47 CFR 0.459.
Needs and Uses: On June 18, 2015,
the Commission adopted a Report and
Order establishing the Numbering
Authorization Application process,
which allows interconnected VoIP
providers to apply for a blanket
authorization from the FCC that, once
granted, will allow them to demonstrate
that they have the authority to provide
service in specific areas, thus enabling
them to request numbers directly from
the Numbering Administrators. This
collection covers the information and
certifications that applicants must
submit in order to comply with the
Numbering Authorization Application
process. The data, information, and
documents acquired through this
collection will allow interconnected
VoIP providers to obtain numbers with
minimal burden or delay while also
preventing providers from obtaining
numbers without first demonstrating
that they can deploy and properly
utilize such resources. This information
will also help the Federal
Communications Commission (FCC)
protect against number exhaust while
promoting competitive neutrality among
traditional telecommunications carriers
and interconnected VoIP providers by
allowing both entities to obtain numbers
directly from the Numbering
Administrators. It will further help the
FCC to maintain efficient utilization of
numbering resources and ensure that
telephone numbers are not being
stranded.
Federal Communications Commission.
Gloria J. Miles,
Federal Register Liaison Officer, Office of the
Secretary.
[FR Doc. 2015–28389 Filed 11–6–15; 8:45 am]
BILLING CODE 6712–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16CA; Docket No. CDC–2015–
0096]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:

The Centers for Disease
Control and Prevention (CDC), as part of

SUMMARY:

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srobinson on DSK5SPTVN1PROD with NOTICES

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Federal Register / Vol. 80, No. 216 / Monday, November 9, 2015 / Notices

its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘Update the Height
Recommendation for Proper Seat Belt
Fit among Children.’’ CDC will use the
information collected to inform CDC’s
child passenger safety recommendation
regarding when children can safely
transition from using a booster seat to
using only a seat belt.
DATES: Written comments must be
received on or before January 8, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0096 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment
should be submitted through the
Federal eRulemaking portal
(Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION:
Under the Paperwork Reduction Act
of 1995 (PRA) (44 U.S.C. 3501–3520),
Federal agencies must obtain approval
from the Office of Management and
Budget (OMB) for each collection of
information they conduct or sponsor. In
addition, the PRA also requires Federal

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agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each new proposed
collection, each proposed extension of
existing collection of information, and
each reinstatement of previously
approved information collection before
submitting the collection to OMB for
approval. To comply with this
requirement, we are publishing this
notice of a proposed data collection as
described below.
Comments are invited 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)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Update the Height Recommendation
for Proper Seat Belt Fit among
Children—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Motor vehicle crashes are a leading
cause of death among children. Proper
restraint use is critical for children in
order to prevent injuries and death in a

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motor vehicle crash. Booster seat use
reduces the risk for serious injury by
45% for children aged 4–8 years when
compared with seat belt use alone. For
older children and adults, seat belt use
reduces the risk for death and serious
injury by approximately half (NHTSA,
2013). Based on this evidence, CDC
recommends using age- and sizeappropriate child restraints (including
child safety seats and booster seats) in
the back seat until adult seat belts fit
properly (i.e. when the lap belt lies
across the upper thighs, not the
stomach; and the shoulder belt lies
across the shoulder and chest, not the
neck or face).
For maximum protection, it is
especially important for children to not
transition to using only a seat belt before
they are large enough for the seat belt
to properly fit. The current
recommendation for when children can
safely transition to a seat belt is 57
inches tall. This height recommendation
of 57 inches was derived from a study
of 155 children aged 6 to 12 years who
were assessed for seat belt fit in 3
different types of vehicles in 1993.
Since 1993, both children and the
vehicle fleet have changed.
The goal of this new collection is to
determine whether the previous height
recommendation for proper seat belt fit
among children is valid in the current
vehicle fleet and among today’s
children. Findings from this data
collection will inform CDC’s child
passenger safety recommendation
regarding when children can safely
transition from using a booster seat with
the vehicle seat belt to using only the
vehicle seat belt. This study will also
provide information on ways to further
reduce motor vehicle-related injuries
and deaths among children. Prospective
study participants will answer a series
of screening questions. Individuals who
meet the screening criteria and are
willing to participate will complete an
in-person measurement session lasting
approximately 2 hours. In-person
measurement sessions will collect data
on 224 children aged 6–12 years. Data
will be analyzed using descriptive
statistics, mean, standard deviation, and
logistic regression.
OMB approval is requested for three
years. Participation in the information
collection is voluntary. There are no
costs to respondents other than their
time.

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Federal Register / Vol. 80, No. 216 / Monday, November 9, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Response burden (hours)

200

1

5/60

17

Seat Belt Fit Measurements ............

75

1

2

150

...........................................................

........................

........................

........................

167

Form name

Parent/guardian of children aged 6–
12 years.
Child participants aged 6–12 years ..

Screener Script Guide ......................

Total ...........................................

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. 2015–28409 Filed 11–6–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘Monitoring and
Reporting for the Core State Violence
and Injury Prevention Program
Cooperative Agreement.’’ CDC will use
the information collected to monitor
cooperative agreement awardees and to
identify challenges to program
implementation and achievement of
outcomes.

SUMMARY:

Written comments must be
received on or before January 8, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0095 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.

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To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited 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)
FOR FURTHER INFORMATION CONTACT:

AGENCY:

DATES:

Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.

[60Day–16–16BZ; Docket No. CDC–2015–
0095]

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Number of
respondents

Type of respondents

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Total burden
hours

ways to enhance the quality, utility, and
clarity of the information to be
collected; (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; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Monitoring and Reporting for the Core
State Violence and Injury Prevention
Program Cooperative Agreement—New
—National Center for Injury Prevention
and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Unintentional and violence-related
injuries and their consequences are the
leading causes of death for the first four
decades of life, regardless of gender,
race, or socioeconomic status. More
than 192,000 individuals in the United
States die each year as a result of
unintentional injuries and violence, and
more than 31 million others suffer nonfatal injuries requiring emergency
department visits each year. Given these
factors, the Public Health Service Act
(PHS Act) provides an important
opportunity for states to advance public
health across the lifespan and to reduce
health disparities. Support and
guidance for these programs have been

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