Att B_ 60d FRN

69225

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: omb@cdc.gov.
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

PO 00000

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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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69226

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

provided through cooperative agreement
funding and technical assistance
administered by CDC’s National Center
for Injury Prevention and Control
(NCIPC). The goal of this ICR is to
collect information needed to monitor
cooperative agreement programs funded
under the Core State Violence and
Injury Prevention Program (Core SVIPP)
(CDC–RFA–CE16–1602).
Information to be collected will
provide crucial data for program
performance monitoring and provide
CDC with the capacity to respond in a
timely manner to requests for
information about the program from the
Department of Health and Human
Services (HHS), the White House,
Congress, and other sources. Awardees
will report progress and activity
information to CDC on an annual
schedule using an Excel-based fillable

technical assistance provided to them,
as needed, to support attainment of their
performance measures. With the tools,
the use of a standard set of data
elements, definitions and specifications
at all levels will help to improve the
quality and comparability of
performance information that is
received by CDC for multiple awardees
and multiple award types by ensuring
that the same information is collected
on all strategies and performance
measures with slightly different areas of
emphasis, depending on the awardee
type (BASE, Enhanced with 1
Component, or Enhanced 2
Components).
OMB approval is requested for three
years. Participation in the information
collection is required as a condition of
funding. There are no costs to
respondents other than their time.

electronic templates. Each awardee will
submit three information collection
tools: Annual Progress Report,
Evaluation and Performance
Management Plan, and Injury Indicator
Spreadsheets. In Year 1, each awardee
will have additional burden related to
initial collection of the reporting tools.
Initial population of the tools is a onetime activity, after completing the initial
population of the tools, pertinent
information only needs to be updated
annually for each report.
CDC will use the information
collected to monitor each awardee’s
progress and to identify facilitators and
challenges to program implementation
and achievement of outcomes.
Monitoring allows CDC to determine
whether an awardee is meeting
performance and goals and to make
adjustments in the type and level of

ESTIMATED ANNUALIZED BURDEN HOURS
Form name

Core SVIPP BASE Awardees ...........

Initial Population-Annual Progress
Report.
Annual Progress Report ...................
Evaluation and Performance Management Plan.
Injury Indicator Spreadsheet ............
Initial Population-Annual Progress
Report.
Annual Progress Report ...................
Evaluation and Performance Management Plan.
Injury Indicator Spreadsheet ............
Initial Population-Annual Progress
Report.
Annual Progress Report ...................
Evaluation and Performance Management Plan.
Injury Indicator Spreadsheet ............
...........................................................

Core SVIPP 1—Enhanced Component Awardees.

Core SVIPP 2—Enhanced Component Awardees.

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

Average
burden per response
(in hours)

20

1

22

440

20
20

1
1

11
2

220
40

20
5

1
1

14
73

280
365

5
5

1
1

58
3

290
15

5
5

1
1

14
146

70
730

5
5

1
1

116
4

580
20

5

1

14

70

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

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

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

3,120

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.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2015–28408 Filed 11–6–15; 8:45 am]

[Docket Number CDC–2015–0075; NIOSH–
288]

BILLING CODE 4163–18–P

srobinson on DSK5SPTVN1PROD with NOTICES

Number of
responses per
respondent

Number of
respondents

Type of respondents

Centers for Disease Control and
Prevention

A Vapor Containment Performance
Protocol for Closed System Transfer
Devices Used During Pharmacy
Compounding and Administration of
Hazardous Drugs; Extension of
Comment Period
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),

AGENCY:

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Total burden
(in hours)

Department of Health and Human
Services (HHS).
ACTION: Notice and extension of
comment period.
On September 8, 2015, the
Director of the National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
published a notice in the Federal
Register [80 FR 53802] announcing the
availability of the following draft
document for public comment entitled
A Vapor Containment Performance
Protocol for Closed System Transfer
Devices Used During Pharmacy
Compounding and Administration of
Hazardous Drugs. Written comments

SUMMARY:

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