Proposed Data Collection Submitted for Public Comment and Recommendations, 47744-47746 [2017-22201]
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47744
Federal Register / Vol. 82, No. 197 / Friday, October 13, 2017 / Notices
during measles cases that have occurred
in the U.S. associated with travel.
The respondents are Cruise Ship
Medical Staff/Cargo Ship Managers and
State/local health department staff.
There is no cost to respondents other
than their time to complete the form and
submit the data to CDC.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Cruise Ship Physicians/
Cargo Ship Managers.
Clinically Active TB Contact Investigation Outcome Reporting Form—Maritime.
Varicella Investigation Outcome Reporting Form
Influenza Like Illness Investigation Outcome Reporting Form.
General Contact Investigation Outcome Reporting Form—Air.
TB Contact Investigation Outcome Reporting
Form—Air.
Measles Contact Investigation Outcome Reporting Form—Air.
Rubella Contact Investigation Outcome Reporting Form—Air.
General Contact Investigation Outcome Reporting Form—Land.
..............................................................................
State/Local public health
staff.
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. 2017–22206 Filed 10–12–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[60Day–17–17BBV; Docket No. CDC–2017–
0085]
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
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 ‘‘Online training for law
enforcement to reduce risks associated
with shift work and long work hours’’.
This study will develop and pilot test a
asabaliauskas on DSKBBXCHB2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:05 Oct 12, 2017
Jkt 244001
20/60
5
29
45
1
1
20/60
20/60
10
15
34
1
5/60
3
547
1
5/60
46
324
1
5/60
27
27
1
5/60
3
15
1
5/60
2
........................
........................
........................
111
You may submit comments,
identified by Docket No. CDC–2017–
0085 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. CDC will post, without
change, all relevant comments to
Regulations.gov.
Please note: Submit all comments
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 Leroy A.
Richardson, Information Collection
Review Office, Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., MS–D74, Atlanta, Georgia
Frm 00058
Fmt 4703
Total burden
(in hours)
1
new, online, interactive training
program tailored for the law
enforcement community that relays the
health and safety risks associated with
shift work, long work hours, and related
workplace sleep issues and presents
strategies for managers and officers to
reduce these risks.
DATES: CDC must receive written
comments on or before December 12,
2017.
PO 00000
Average
burden per
response
(in hours)
15
ADDRESSES:
Centers for Disease Control and
Prevention
Number of
responses per
respondent
Sfmt 4703
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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected; and
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
E:\FR\FM\13OCN1.SGM
13OCN1
47745
Federal Register / Vol. 82, No. 197 / Friday, October 13, 2017 / Notices
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses.
5. Assess information collection costs.
Proposed Project
Online Training for Law Enforcement
to Reduce Risks Associated with Shift
Work and Long Work Hours—NEW—
National Institute for Occupational
Safety and Health, Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Law enforcement officers work in
stressful and dangerous conditions to
enforce law and order, prevent crime,
and protect persons and property. Police
often work during the evening, at night,
and sometimes irregular and long hours.
Shift work and long work hours are
linked to many health and safety risks
due to disturbances to sleep, circadian
rhythms, and personal relationships.
These work schedules and inadequate
sleep are likely critical contributors to
the many health problems seen in
police: shorter life spans, high
occupational injury rates, and burden of
chronic illnesses. One important
strategy to reduce these risks is training
programs to inform employers and law
enforcement officers about the risks and
strategies to reduce the risks. This is a
new Information Collection Request for
1 year of data collection. The
Occupational Safety and Health Act of
1970 authorizes the National Institute
for Occupational Safety and Health to
carry out this data collection.
The purpose of this project is to
develop a training program to relay the
risks linked to shift work and long work
hours and give workplace strategies for
employers and personal strategies for
the officers to reduce the risks. Once
provide feedback about the training, to
include barriers to using the training
information and what influential people
in their life would want them to do with
the training information. At the end of
week 4, the respondent will return the
actigraph. No data collection will occur
during weeks 5 to 9 of the study.
The second post-test period will be
weeks 11 and 12 of the study (weeks 8
and 9 after the training) to gather longerterm outcomes. At the beginning of
week 11, the respondents will be fitted
with another ACTi graph. The
respondent will wear the ACTi graph
and complete the sleep activity diary for
the next 14 days. At the end of week 12
of the study, respondent will complete
the Epworth Sleepiness Scale,
Pittsburgh Sleep Quality Index, and
Changes in Behaviors after Training.
The combined response time is 5
minutes. The respondent will return the
ACTi graph and study ends.
The burden table lists three 10-minute
meetings during the post-test period
when they will return the ACTi graph
at the end of week 4, be fitted with an
ACTi graph at the beginning of week 11
and return it at the end of week 12. The
respondents will complete the sleep
activity diary for 42 days total for 2
minutes each day. The total burden
hours is 84.
CDC will use the findings from the
pilot test to make improvements to the
training program. The research team
will reinforce or expand training
content that showed less than desired
results on the pilot test. Potential
impacts of this project include
improvements in management practices
such as the design of work schedules
and improvements in officers’ personal
behaviors for coping with the demands
of shift work and long work hours. The
total estimated annualized burden hours
is 389. There are no costs to respondents
other than their time.
finalized, the training will be available
on the NIOSH Web site.
The training will be pilot tested with
30 recent graduates of a police academy
in their first field experience and 30
experienced officers. CDC will recruit
sixty law enforcement officers during a
15-minute phone call. All will work full
time on fixed night shifts. The pilot test
will use a pretest and posttest design to
examine sleep (both duration and
quality), worktime sleepiness, and
knowledge retained. Pre-test measures
will be collected 2 weeks before the
training. CDC will collect post-test
measures the week of the training, 1
week after the training and at 8 and 9
weeks after the training. Additional
post-test measures will include feedback
about the training and if specific
behaviors changed.
Before starting the pretest, the
respondent will sign an informed
consent form. The pilot pre-test will
start with the respondent filling out a 10
minute online survey that includes four
short surveys: (1) Demographic
information and work experience; (2)
the Epworth Sleepiness Scale; (3) the
Pittsburgh Sleep Quality Index; and (4)
a knowledge test. The respondent will
be fitted with a wrist actigraph, which
will record activity and estimate the
times of sleep. The respondents will
keep an online sleep activity diary and
wear the actigraph continuously during
weeks 1 to 4 of the study. The online
sleep activity diary takes approximately
2 minutes a day to complete. The sleep
diary and actigraph are being used
together to obtain a more accurate
timing of respondent’s sleep and
activity.
During the third week of the study,
the respondent will participate in a 3.5hour online training program.
Immediately after completing the
training, the respondent will take the
post-test knowledge test and will
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Law enforcement officers ..................
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Type of respondents
Initial phone call to recruit participation.
Informed consent .............................
Knowledge survey ............................
Epworth Sleepiness Scale ...............
Pittsburgh Sleep Quality Index ........
Demographics and work experience
Sleep diary .......................................
Online training ..................................
Feedback about Training, Barriers,
and Influential People.
Changes in Behaviors after Training
Law
Law
Law
Law
Law
Law
Law
Law
enforcement
enforcement
enforcement
enforcement
enforcement
enforcement
enforcement
enforcement
officers
officers
officers
officers
officers
officers
officers
officers
..................
..................
..................
..................
..................
..................
..................
..................
Law enforcement officers ..................
VerDate Sep<11>2014
18:05 Oct 12, 2017
Jkt 244001
PO 00000
Frm 00059
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden
(in hours)
60
1
15/60
15
60
60
60
60
60
60
60
60
1
5
2
2
1
42
1
1
10/60
5/60
1/60
2/60
2/60
2/60
3.5
5/60
10
25
2
4
2
84
210
5
60
1
2/60
2
E:\FR\FM\13OCN1.SGM
13OCN1
47746
Federal Register / Vol. 82, No. 197 / Friday, October 13, 2017 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total
burden
(in hours)
Type of respondents
Form name
Law enforcement officers ..................
Actigraph fitting and return ...............
60
3
10/60
30
Total ...........................................
...........................................................
........................
........................
........................
389
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. 2017–22201 Filed 10–12–17; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–17–17ND]
asabaliauskas on DSKBBXCHB2PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on February
10, 2017 to obtain comments from the
public and affected agencies. CDC
received one comment related to the
previous notice. The purpose of this
notice is to allow an additional 30 days
for public comments.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. The Office
of Management and Budget is
particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
VerDate Sep<11>2014
18:05 Oct 12, 2017
Jkt 244001
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW.,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
Annual Progress Report (APR) for
Injury Control Research Centers
(ICRC)—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Injury Control Research Centers
(ICRCs) form a national network of ten
comprehensive academic research
centers that focus on three core
functions: Research, training, and
outreach. ICRCs are on the scientific
front line conducting cutting-edge,
multidisciplinary research on the
causes, outcomes, and prevention of
injuries and violence.
ICRC research focuses on issues of
local and national importance including
motor vehicle injuries; interpersonal
violence and suicide; opioid overdoses;
older adult falls; and traumatic brain
injuries. ICRCs work with states and
communities to ensure research is put
into action to prevent injuries and
violence. They provide technical
assistance to disseminate and translate
research findings which leads to
increased awareness and influences
action. ICRCs play a critical role training
PO 00000
Frm 00060
Fmt 4703
Sfmt 4703
and developing the current and next
generation of researchers and public
health professionals. This helps ensure
there is an adequate supply of qualified
practitioners and researchers to advance
prevention research, address new
problems, and reach new populations
across the nation.
The CDC seeks OMB approval for
three years to collect Annual Progress
Report (APR) information from 10
grantees funded under Grants for Injury
Control Research Centers (ICRC). ICRC
awardees will report activity
information to CDC annually using three
fillable electronic templates. The first
Word-based template is the principal
tool for the Indicators Data Collection
(IDC), which is based on a set of
program activity indicators and key
ICRC evaluation questions. The second
Word-based template collects
information about non-CDC-funded
studies, and the third template, which is
Excel-based, collects information about
ICRC personnel and publications.
Information will be reported
electronically to the NCIPC for program
monitoring, and hard copies will be
submitted to CDC’s Office of Financial
Resources (OFR). Together, the tools
describe grantees’ annual goals,
objectives, progress, and performance
towards overall cooperative agreement
aims. The tools also describe how
grantees implement and use evidencebased injury prevention and control
strategies.
Information to be collected will
provide crucial data for program
performance monitoring, will allow
CDC to analyze and synthesize
information from grantees, help ensure
consistency in documenting progress
and technical assistance, enhance
accountability of the use of federal
funds, and provide timely reports as
frequently requested by the Department
of Health and Human Services, the
White House, and Congress.
Submission of the Annual Progress
Report is required for cooperative
agreement grantees. The total estimated
annualized burden hours are 500. There
is no cost to respondents other than
their time.
E:\FR\FM\13OCN1.SGM
13OCN1
]]>Agencies
[Federal Register Volume 82, Number 197 (Friday, October 13, 2017)]
[Notices]
[Pages 47744-47746]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-22201]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-17-17BBV; Docket No. CDC-2017-0085]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: 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 ``Online training
for law enforcement to reduce risks associated with shift work and long
work hours''. This study will develop and pilot test a new, online,
interactive training program tailored for the law enforcement community
that relays the health and safety risks associated with shift work,
long work hours, and related workplace sleep issues and presents
strategies for managers and officers to reduce these risks.
DATES: CDC must receive written comments on or before December 12,
2017.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2017-
0085 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. CDC will post, without change, all relevant comments
to Regulations.gov.
Please note: Submit all comments 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 Leroy A. Richardson, 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 the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected; and
4. Minimize the burden of the collection of information on those
who are to respond, including through the
[[Page 47745]]
use of appropriate automated, electronic, mechanical, or other
technological collection techniques or other forms of information
technology, e.g., permitting electronic submissions of responses.
5. Assess information collection costs.
Proposed Project
Online Training for Law Enforcement to Reduce Risks Associated with
Shift Work and Long Work Hours--NEW--National Institute for
Occupational Safety and Health, Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Law enforcement officers work in stressful and dangerous conditions
to enforce law and order, prevent crime, and protect persons and
property. Police often work during the evening, at night, and sometimes
irregular and long hours. Shift work and long work hours are linked to
many health and safety risks due to disturbances to sleep, circadian
rhythms, and personal relationships. These work schedules and
inadequate sleep are likely critical contributors to the many health
problems seen in police: shorter life spans, high occupational injury
rates, and burden of chronic illnesses. One important strategy to
reduce these risks is training programs to inform employers and law
enforcement officers about the risks and strategies to reduce the
risks. This is a new Information Collection Request for 1 year of data
collection. The Occupational Safety and Health Act of 1970 authorizes
the National Institute for Occupational Safety and Health to carry out
this data collection.
The purpose of this project is to develop a training program to
relay the risks linked to shift work and long work hours and give
workplace strategies for employers and personal strategies for the
officers to reduce the risks. Once finalized, the training will be
available on the NIOSH Web site.
The training will be pilot tested with 30 recent graduates of a
police academy in their first field experience and 30 experienced
officers. CDC will recruit sixty law enforcement officers during a 15-
minute phone call. All will work full time on fixed night shifts. The
pilot test will use a pretest and posttest design to examine sleep
(both duration and quality), worktime sleepiness, and knowledge
retained. Pre-test measures will be collected 2 weeks before the
training. CDC will collect post-test measures the week of the training,
1 week after the training and at 8 and 9 weeks after the training.
Additional post-test measures will include feedback about the training
and if specific behaviors changed.
Before starting the pretest, the respondent will sign an informed
consent form. The pilot pre-test will start with the respondent filling
out a 10 minute online survey that includes four short surveys: (1)
Demographic information and work experience; (2) the Epworth Sleepiness
Scale; (3) the Pittsburgh Sleep Quality Index; and (4) a knowledge
test. The respondent will be fitted with a wrist actigraph, which will
record activity and estimate the times of sleep. The respondents will
keep an online sleep activity diary and wear the actigraph continuously
during weeks 1 to 4 of the study. The online sleep activity diary takes
approximately 2 minutes a day to complete. The sleep diary and
actigraph are being used together to obtain a more accurate timing of
respondent's sleep and activity.
During the third week of the study, the respondent will participate
in a 3.5-hour online training program. Immediately after completing the
training, the respondent will take the post-test knowledge test and
will provide feedback about the training, to include barriers to using
the training information and what influential people in their life
would want them to do with the training information. At the end of week
4, the respondent will return the actigraph. No data collection will
occur during weeks 5 to 9 of the study.
The second post-test period will be weeks 11 and 12 of the study
(weeks 8 and 9 after the training) to gather longer-term outcomes. At
the beginning of week 11, the respondents will be fitted with another
ACTi graph. The respondent will wear the ACTi graph and complete the
sleep activity diary for the next 14 days. At the end of week 12 of the
study, respondent will complete the Epworth Sleepiness Scale,
Pittsburgh Sleep Quality Index, and Changes in Behaviors after
Training. The combined response time is 5 minutes. The respondent will
return the ACTi graph and study ends.
The burden table lists three 10-minute meetings during the post-
test period when they will return the ACTi graph at the end of week 4,
be fitted with an ACTi graph at the beginning of week 11 and return it
at the end of week 12. The respondents will complete the sleep activity
diary for 42 days total for 2 minutes each day. The total burden hours
is 84.
CDC will use the findings from the pilot test to make improvements
to the training program. The research team will reinforce or expand
training content that showed less than desired results on the pilot
test. Potential impacts of this project include improvements in
management practices such as the design of work schedules and
improvements in officers' personal behaviors for coping with the
demands of shift work and long work hours. The total estimated
annualized burden hours is 389. There are no costs to respondents other
than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Law enforcement officers...... Initial phone 60 1 15/60 15
call to recruit
participation.
Law enforcement officers...... Informed consent 60 1 10/60 10
Law enforcement officers...... Knowledge survey 60 5 5/60 25
Law enforcement officers...... Epworth 60 2 1/60 2
Sleepiness
Scale.
Law enforcement officers...... Pittsburgh Sleep 60 2 2/60 4
Quality Index.
Law enforcement officers...... Demographics and 60 1 2/60 2
work experience.
Law enforcement officers...... Sleep diary..... 60 42 2/60 84
Law enforcement officers...... Online training. 60 1 3.5 210
Law enforcement officers...... Feedback about 60 1 5/60 5
Training,
Barriers, and
Influential
People.
Law enforcement officers...... Changes in 60 1 2/60 2
Behaviors after
Training.
[[Page 47746]]
Law enforcement officers...... Actigraph 60 3 10/60 30
fitting and
return.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 389
----------------------------------------------------------------------------------------------------------------
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. 2017-22201 Filed 10-12-17; 8:45 am]
BILLING CODE 4163-18-P
