Proposed Data Collection Submitted for Public Comment and Recommendations, 46680-46682 [2016-16873]
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46680
Federal Register / Vol. 81, No. 137 / Monday, July 18, 2016 / Notices
previously approved for the 2013–2014
survey. Minor changes to survey content
will be made to eliminate unnecessary
questions, add new questions of
interest, and improve formatting,
usability, and data quality. As in 2013–
2014, different versions of the survey
instrument will be administered to
providers and clinic administrators. The
estimated burden per response for
providers is 15 minutes and has not
changed since the previous OMB
approval. The estimated burden per
response for administrators will be
reduced from 40 minutes to 25 minutes.
Private-sector physicians will be
randomly selected from sampling
frames with individual-level
information on physicians. To reach
public-sector providers and clinic
administrators, publicly funded clinics
will be randomly selected; one provider
and the clinic administrator will be
asked to complete surveys at sampled
clinics. Specifically, surveys will be
completed by: (a) 2,000 private-sector
office-based physicians (i.e., those
specializing in obstetrics/gynecology,
family medicine, and adolescent
medicine), sampled from the American
Medical Association Physician
Masterfile; (b) 2,000 providers from
Title X clinics, sampled from a database
of publicly funded family planning
clinics; (c) 2,000 providers from nonTitle X clinics, sampled from a database
of publicly funded family planning
clinics; (d) 2,000 clinic administrators
from Title X clinics, sampled from a
database of publicly funded family
planning clinics; and (e) 2,000 clinic
administrators from non-Title X clinics,
sampled from a database of publicly
funded family planning clinics.
Each sampled provider and clinic will
receive a mailed survey package. For
private-sector family planning
providers, each mailed survey package
will include a single survey to be
completed by the provider. For publicsector clinics, each mailed survey
package will include two surveys—one
to be completed by a randomly selected
family planning provider at the clinic,
and the second to be completed by the
clinic administrator. Each mailed survey
will be accompanied by a postage-paid
return envelope. Individuals will also be
given the option to complete the survey
online via a password protected webbased data collection system.
OMB approval is requested for one
year. Participation is voluntary and
there are no costs to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number
responses per
respondent
Average
burden per
response
(in hr)
Total burden
(in hr)
Type of respondents
Form name
Office-based physicians (private sector).
Title X clinic providers (public sector)
2017 Survey of Health Care Providers.
2017 Survey of Health Care Providers.
2017 Survey of Health Care Providers.
2017 Survey of Administrators of
Publicly-Funded Health Centers
that Provide Family Planning.
2017 Survey of Administrators of
Publicly-Funded Health Centers
that Provide Family Planning.
2,000
1
15/60
500
2,000
1
15/60
500
2,000
1
15/60
500
2,000
1
25/60
834
2,000
1
25/60
834
...........................................................
........................
........................
........................
3,168
Non-Title X publicly funded clinic
providers (public sector).
Title X clinic administrators (public
sector).
Non-Title X publicly funded clinic administrators (public sector).
Total ...........................................
Jeffrey M. Zirger,
Acting 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. 2016–16874 Filed 7–15–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Centers for Disease Control and
Prevention
[Docket No. CDC–2016–0063; 60Day–16–
16AVC]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
VerDate Sep<11>2014
17:52 Jul 15, 2016
Jkt 238001
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 ‘‘Generic Clearance for
CDC/ATSDR Formative Research and
Tool Development’’. This information
collection request is designed to allow
CDC to conduct formative research
information collection activities used to
inform aspects of surveillance,
communications, health promotion, and
research project development.
DATES: Written comments must be
received on or before September 16,
2016.
SUMMARY:
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
You may submit comments,
identified by Docket No. CDC–2016–
0063 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Jeffrey M. Zirger, 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.
ADDRESSES:
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.
E:\FR\FM\18JYN1.SGM
18JYN1
Federal Register / Vol. 81, No. 137 / Monday, July 18, 2016 / Notices
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.
FOR FURTHER INFORMATION CONTACT:
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)
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.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
17:52 Jul 15, 2016
Jkt 238001
Proposed Project
Generic Clearance for CDC/ATSDR
Formative Research and Tool
Development (CDC)
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) requests approval for
a new generic clearance for CDC/ATSDR
Formative Research and Tool
Development. This information
collection request is designed to allow
CDC to conduct formative research
information collection activities used to
inform many aspects of surveillance,
communications, health promotion, and
research project development at CDC.
Formative research is the basis for
developing effective strategies including
communication channels, for
influencing behavior change. It helps
researchers identify and understand the
characteristics—interests, behaviors and
needs—of target populations that
influence their decisions and actions.
Formative research is integral in
developing programs as well as
improving existing and ongoing
programs. Formative research looks at
the community in which a public health
intervention is being or will be
implemented and helps the project staff
understand the interests, attributes and
needs of different populations and
persons in that community. Formative
research occurs before a program is
designed and implemented, or while a
program is being conducted.
At CDC formative research is
necessary for developing new programs
or adapting programs that deal with the
complexity of behaviors, social context,
cultural identities, and health care that
underlie the epidemiology of diseases
and conditions in the U.S. CDC
conducts formative research to develop
public-sensitive communication
messages and user friendly tools prior to
developing or recommending
interventions, or care. Sometimes these
studies are entirely behavioral but most
often they are cycles of interviews and
focus groups designed to inform the
development of a product.
Products from these formative
research studies will be used for
prevention of disease. Findings from
these studies may also be presented as
evidence to disease-specific National
Advisory Committees, to support
revisions to recommended prevention
and intervention methods, as well as
new recommendations.
Much of CDC’s health communication
takes place within campaigns that have
fairly lengthy planning periods—
timeframes that accommodate the
standard Federal process for approving
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
46681
data collections. Short term qualitative
interviewing and cognitive research
techniques have previously proven
invaluable in the development of
scientifically valid and populationappropriate methods, interventions, and
instruments.
This request includes studies
investigating the utility and
acceptability of proposed sampling and
recruitment methods, intervention
contents and delivery, questionnaire
domains, individual questions, and
interactions with project staff or
electronic data collection equipment.
These activities will also provide
information about how respondents
answer questions and ways in which
question response bias and error can be
reduced.
This request also includes collection
of information from public health
programs to assess needs related to
initiation of a new program activity or
expansion or changes in scope or
implementation of existing program
activities to adapt them to current
needs. The information collected will be
used to advise programs and provide
capacity-building assistance tailored to
identify needs.
Overall, these development activities
are intended to provide information that
will increase the success of the
surveillance or research projects
through increasing response rates and
decreasing response error, thereby
decreasing future data collection burden
to the public. The studies that will be
covered under this request will include
one or more of the following
investigational modalities: (1)
Structured and qualitative interviewing
for surveillance, research, interventions
and material development, (2) cognitive
interviewing for development of specific
data collection instruments, (3)
methodological research (4) usability
testing of technology-based instruments
and materials, (5) field testing of new
methodologies and materials, (6)
investigation of mental models for
health decision-making, to inform
health communication messages, and (7)
organizational needs assessments to
support development of capacity.
Respondents who will participate in
individual and group interviews
(qualitative, cognitive, and computer
assisted development activities) are
selected purposively from those who
respond to recruitment advertisements.
In addition to utilizing advertisements
for recruitment, respondents who will
participate in research on survey
methods may be selected purposively or
systematically from within an ongoing
surveillance or research project.
E:\FR\FM\18JYN1.SGM
18JYN1
46682
Federal Register / Vol. 81, No. 137 / Monday, July 18, 2016 / Notices
Participation of respondents is
voluntary.
There is no cost to participants other
than their time. The total estimated
annual burden is 8,000 hours.
Form name
General public and health care providers.
Average hours
per response
Total response
burden
(hrs.)
4,000
2,000
2,000
2,000
2,000
1
1
1
1
1
10/60
10/60
1
2
30/60
667
333
2,000
4,000
1,000
........................
........................
........................
8,000
Screener ..........................................
Consent Forms ................................
Interview ...........................................
Focus group interview .....................
Survey ..............................................
Total ...........................................
..........................................................
Jeffrey M. Zirger,
Acting 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. 2016–16873 Filed 7–15–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Privacy Act of 1974; System of
Records Notice
Department of Health and
Human Services (HHS), Administration
for Children and Families (ACF), Office
of Refugee Resettlement (ORR).
ACTION: Notice to establish five new and
delete one Privacy Act systems of
records.
AGENCY:
In accordance with the
requirements of the Privacy Act of 1974,
as amended (5 U.S.C. 552a), the Office
of Refugee Resettlement (ORR) within
HHS’ Administration for Children and
Families (ACF) is establishing five new
systems of records: 09–80–0321 ORR
Division of Children’s Services Records;
09–80–0325 ORR Internet Refugee
Arrivals Data System (iRADS); 09–80–
0327 ORR Repatriation Program
Records; 09–80–0329 ORR
Unaccompanied Refugee Minors
Records; and 09–80–0388 ORR Refugee
Suicide Database. ORR is deleting one
system of records, 09–60–0217 ORR
Cuban Refugee Data System, which is
being replaced by the new iRADS
system of records.
Four of the five new systems of
records are ‘‘mixed,’’ in that they
contain records pertaining to both U.S.
persons (i.e., individuals who are
citizens of the United States or aliens
lawfully admitted for permanent
residence in the United States) and nonU.S. persons.
SUMMARY:
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Type of respondent
VerDate Sep<11>2014
17:52 Jul 15, 2016
Jkt 238001
The Privacy Act applies only to U.S.
persons (citizens of the United States or
aliens lawfully admitted for permanent
residence in the United States). As a
matter of discretion, ORR will treat
information that it maintains in its
mixed systems of records as being
subject to the provisions of the Privacy
Act, regardless of whether the
information relates to U.S. persons
covered by the Privacy Act.
This policy implements a 1975 Office
of Management and Budget (OMB)
recommendation to apply, as a matter of
policy, the administrative provisions of
the Privacy Act to records about nonU.S. persons in mixed systems of
records (referred to as the non-U.S.
persons policy).
DATES: This Notice will become
effective 30 days after publication,
unless the Office of Refugee
Resettlement makes changes based on
comments received. Written comments
should be submitted on or before the
effective date.
ADDRESSES: The public should address
written comments to Gary Cochran,
Senior Agency Officer for Privacy, by
mail at Administration for Children and
Families, Mary E. Switzer Building, 330
C Street SW., Washington, DC 20201, or
by email at gary.cochran@acf.hhs.gov.
FOR FURTHER INFORMATION CONTACT:
Questions should be directed to the
contact person for the system in
question:
1. 09–80–0321 ORR Division of
Children’s Services Records
Jallyn Sualog, Administration for
Children and Families, ORR, Mary
E. Switzer Building, 330 C Street
SW., Washington, DC 20201; Email:
Jallyn.Sualog@acf.hhs.gov.
2. 09–80–0325 ORR Internet Refugee
Arrivals Data System (iRADS)
Joann Simmons, Administration for
Children and Families, ORR, Mary
E. Switzer Building, 330 C Street
SW., Washington, DC 20201; Email:
joann.simmons@acf.hhs.gov.
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
3. 09–80–0327 ORR Repatriation
Program Records
Elizabeth Russell, Administration for
Children and Families, ORR, Mary
E. Switzer Building, 330 C Street
SW., Washington, DC 20201; Email:
Elizabeth.russell@acf.hhs.gov.
4. 09–80–0329 ORR Unaccompanied
Refugee Minors Records
Jallyn Sualog, Administration for
Children and Families, ORR, Mary
E. Switzer Building, 330 C Street
SW., Washington, DC 20201; Email:
Jallyn.Sualog@acf.hhs.gov
5. 09–80–0388 ORR Refugee Suicide
Database
Dr. Curi Kim, Administration for
Children and Families, ORR, Mary
E. Switzer Building, 330 C Street
SW., Washington, DC 20201; Email:
curi.kim@acf.hhs.gov.
SUPPLEMENTARY INFORMATION
I. Background on Five New Systems of
Records
The five new systems of records
established in this Notice are
maintained by the Office of Refugee
Resettlement (ORR) within HHS’
Administration for Children and
Families (ACF); ORR plans, develops,
and directs the implementation of a
domestic resettlement assistance
program for refugees and other eligible
populations. ORR provides resources to
assist these populations with successful
integration into American society.
ORR’s social services help refugees
become self-sufficient as quickly as
possible after their arrival in the United
States. ORR also provides guidance,
resources, and oversight for specific
health challenges including medical
assistance, initial health screenings, and
consultations. ORR also oversees the
Unaccompanied Children Program,
providing care for unaccompanied
children without lawful immigration
status, and the U.S. Repatriation
Program, providing loans to eligible
repatriates referred from the U.S.
Department of State.
E:\FR\FM\18JYN1.SGM
18JYN1
]]>Agencies
[Federal Register Volume 81, Number 137 (Monday, July 18, 2016)]
[Notices]
[Pages 46680-46682]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-16873]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[Docket No. CDC-2016-0063; 60Day-16-16AVC]
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 ``Generic
Clearance for CDC/ATSDR Formative Research and Tool Development''. This
information collection request is designed to allow CDC to conduct
formative research information collection activities used to inform
aspects of surveillance, communications, health promotion, and research
project development.
DATES: Written comments must be received on or before September 16,
2016.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0063 by any of the following methods:
Federal eRulemaking Portal: Regulations.gov. Follow the
instructions for submitting comments.
Mail: Jeffrey M. Zirger, 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.
[[Page 46681]]
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: 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) 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
Generic Clearance for CDC/ATSDR Formative Research and Tool Development
(CDC)
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) requests
approval for a new generic clearance for CDC/ATSDR Formative Research
and Tool Development. This information collection request is designed
to allow CDC to conduct formative research information collection
activities used to inform many aspects of surveillance, communications,
health promotion, and research project development at CDC. Formative
research is the basis for developing effective strategies including
communication channels, for influencing behavior change. It helps
researchers identify and understand the characteristics--interests,
behaviors and needs--of target populations that influence their
decisions and actions.
Formative research is integral in developing programs as well as
improving existing and ongoing programs. Formative research looks at
the community in which a public health intervention is being or will be
implemented and helps the project staff understand the interests,
attributes and needs of different populations and persons in that
community. Formative research occurs before a program is designed and
implemented, or while a program is being conducted.
At CDC formative research is necessary for developing new programs
or adapting programs that deal with the complexity of behaviors, social
context, cultural identities, and health care that underlie the
epidemiology of diseases and conditions in the U.S. CDC conducts
formative research to develop public-sensitive communication messages
and user friendly tools prior to developing or recommending
interventions, or care. Sometimes these studies are entirely behavioral
but most often they are cycles of interviews and focus groups designed
to inform the development of a product.
Products from these formative research studies will be used for
prevention of disease. Findings from these studies may also be
presented as evidence to disease-specific National Advisory Committees,
to support revisions to recommended prevention and intervention
methods, as well as new recommendations.
Much of CDC's health communication takes place within campaigns
that have fairly lengthy planning periods--timeframes that accommodate
the standard Federal process for approving data collections. Short term
qualitative interviewing and cognitive research techniques have
previously proven invaluable in the development of scientifically valid
and population-appropriate methods, interventions, and instruments.
This request includes studies investigating the utility and
acceptability of proposed sampling and recruitment methods,
intervention contents and delivery, questionnaire domains, individual
questions, and interactions with project staff or electronic data
collection equipment. These activities will also provide information
about how respondents answer questions and ways in which question
response bias and error can be reduced.
This request also includes collection of information from public
health programs to assess needs related to initiation of a new program
activity or expansion or changes in scope or implementation of existing
program activities to adapt them to current needs. The information
collected will be used to advise programs and provide capacity-building
assistance tailored to identify needs.
Overall, these development activities are intended to provide
information that will increase the success of the surveillance or
research projects through increasing response rates and decreasing
response error, thereby decreasing future data collection burden to the
public. The studies that will be covered under this request will
include one or more of the following investigational modalities: (1)
Structured and qualitative interviewing for surveillance, research,
interventions and material development, (2) cognitive interviewing for
development of specific data collection instruments, (3) methodological
research (4) usability testing of technology-based instruments and
materials, (5) field testing of new methodologies and materials, (6)
investigation of mental models for health decision-making, to inform
health communication messages, and (7) organizational needs assessments
to support development of capacity. Respondents who will participate in
individual and group interviews (qualitative, cognitive, and computer
assisted development activities) are selected purposively from those
who respond to recruitment advertisements.
In addition to utilizing advertisements for recruitment,
respondents who will participate in research on survey methods may be
selected purposively or systematically from within an ongoing
surveillance or research project.
[[Page 46682]]
Participation of respondents is voluntary.
There is no cost to participants other than their time. The total
estimated annual burden is 8,000 hours.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of
Type of respondent Form name Number of responses per Average hours Total response
respondents respondent per response burden (hrs.)
--------------------------------------------------------------------------------------------------------------------------------------------------------
General public and health care providers....... Screener............................... 4,000 1 10/60 667
Consent Forms.......................... 2,000 1 10/60 333
Interview.............................. 2,000 1 1 2,000
Focus group interview.................. 2,000 1 2 4,000
Survey................................. 2,000 1 30/60 1,000
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 8,000
--------------------------------------------------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Acting 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. 2016-16873 Filed 7-15-16; 8:45 am]
BILLING CODE 4163-18-P
