Proposed Data Collection Submitted for Public Comment and Recommendations, 34645-34647 [2015-14787]
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34645
Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices
typically consists of one moderator and
4 to 10 participants, depending on the
research question. In-depth or
ethnographic interviews are one-on-one
interviews designed to elicit the
understandings or terminology that are
necessary for question design, as well as
to gather detailed information that can
contribute to the analysis of both
qualitative and quantitative data.
Usability tests are typically one-on-one
interviews that are used to determine
how a given survey or information
collection tool functions in the field,
and how the mode and layout of the
instrument itself may contribute to
Additionally, field or pilot tests may be
conducted on both representative and
non-representative samples, including
those obtained from commercial survey
and web panel vendors. Beyond looking
at traditional measures of survey errors
(such as missing rates, item nonresponse, and don’t know rates), these
pilot tests can be used to run
experimental designs in order to capture
how different questions function in a
field setting.
There are no costs to respondents
other than their time. The total
estimated annual burden hours are
4,383.
survey response error and the survey
response process.
In addition to these qualitative
methods, NCHS also uses various tools
to obtain quantitative data, which can
be analyzed alone or analyzed alongside
qualitative data to give a much fuller
accounting of the survey response
process. For instance, phone, internet,
mail, and in-person follow-up
interviews of previous NCHS survey
respondents may be used to test the
validity of survey questions and
questionnaires and to obtain more
detailed information that cannot be
gathered on the original survey.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Individuals or households ..............................
Individuals or households ..............................
Individuals or households ..............................
Eligibility Screeners .......................................
Developmental Questionnaires .....................
Focus group documents ...............................
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. 2015–14786 Filed 6–16–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–15–0134; Docket No. CDC–2015–
0039]
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 a revision to several of the
information collections pertaining to the
importation of dogs as outlined in the
currently approved information
asabaliauskas on DSK5VPTVN1PROD with NOTICES
SUMMARY:
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18:47 Jun 16, 2015
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collection entitled ‘‘Foreign Quarantine
Regulations (42 CFR part 71)’’.
DATES: Written comments must be
received on or before August 17, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0039 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.
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)
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
4,000
3,900
100
Number of
responses per
respondent
Average burden
per response
(in hrs.)
1
1
1
5/60
1
1.5
(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
E:\FR\FM\17JNN1.SGM
17JNN1
34646
Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices
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
Foreign Quarantine Regulations (42
CFR part 71)—Revision—(OMB Control
No. 0920–0134, Expires September 30,
2017), National Center for Emerging and
Zoonotic Infections Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
This information collection revision
request is an effort to provide greater
clarity surrounding paperwork
requirements and focuses exclusively on
certain information collections that
• CDC will include one modified IC:
‘‘71.51(c)(2), (d) Application For
Permission To Import A Dog
Unimmunized Against Rabies’’. This
will include a reduced estimate of the
numbers of these permits, formerly CDC
form 75.37 NOTICE TO OWNERS AND
IMPORTERS OF DOGS: Requirement for
Dog Confinement, issued each year.
• CDC will include a separate IC
pertaining to 71.51(c)(1), (d). The title
for this IC is Valid Rabies Vaccination
Certificate, which will include only the
burden associated with rabies
vaccination certificates.
• CDC is also including an
information collection for 71.51(c)(i),
(ii), and (iii) which provides exemption
criteria for the importation of a dog
without a rabies vaccination certificate.
CDC is not requesting changes to any
of the other information collections
included under OMB control number
0920–0134.
The total requested burden hours is
307,613. There is no burden to
respondents other than the time taken to
complete the reports or documentation
for CDC.
pertain to importation of dogs into the
United States. Specifically, CDC seeks to
make the following changes:
• CDC is asking to correct a
transcription error in the burden tables
in section 12. Currently, the relevant IC
reads: 71.51(b)(2) Dogs/cats:
Certification of Confinement,
Vaccination (CDC form 75.37). It should
have been: 71.51(c)(2) Dogs:
Certification of Confinement,
Vaccination (CDC form 75.37).
• CDC is also proposing to replace the
CDC form 75.37 NOTICE TO OWNERS
AND IMPORTERS OF DOGS:
Requirement for Dog Confinement with
a new Application For Permission To
Import A Dog Unimmunized Against
Rabies, which, if the importer meets the
criteria for importation, will be followed
by a CDC-completed Permit to
Conditionally Import a Dog
Inadequately Immunized against
Rabies—Single Entry
• CDC is also requesting approval to
change and split the current information
collection (IC) ‘‘71.51(c)(2) Dogs/cats:
Certification of Confinement,
Vaccination (CDC form 75.37)’’ into two
separate ICs.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name/CFR reference
Maritime conveyance operators ........
71.21(a) Radio Report of death/illness—illness reports from ships
(fillable PDF (individual case and
cumulative report), phone, transcribed email).
71.21(b) Death/Illness reports from
aircrafts (verbal, no form).
71.21(c) Gastrointestinal Illnesses
reports 24 and 4 hours before arrival (MIDRS).
71.21(c)
Recordkeeping—Medical
logs (no form, captains provide
logs).
71.33(c) Report by persons in isolation or surveillance (verbal, no
form).
71.35 Report of death/illness during
stay in port (verbal, no form).
Locator Form used in an outbreak
of public health significance.
Locator Form used for reporting of
an ill passenger(s).
71.51(c)(1), (d)—Valid Rabies Vaccination Certificates.
71.51(c)(i), (ii), and (iii) exemption
criteria for the importation of a
dog without a rabies vaccination
certificate.
71.51(c)(2), (d) Application For Permission To Import A Dog
Unimmunized Against Rabies.
71.51(b) (3) Dogs/cats: Record of
sickness or deaths (no form,
record review).
Aircraft commander or operators ......
Maritime conveyance operators ........
Maritime conveyance operators ........
Isolated or Quarantined individuals ..
Maritime conveyance operators ........
Traveler .............................................
Traveler .............................................
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Importer .............................................
Importer .............................................
Importer .............................................
Importer .............................................
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Frm 00041
Fmt 4703
Number of
responses per
respondent
Number of
respondents
Type of respondent
Sfmt 4703
Average
burden per
response
(in hours)
Total burden
hours
2,000
1
2/60
67
1,700
1
2/60
57
17,000
1
3/60
850
17,000
1
3/60
850
11
1
3/60
1
5
1
30/60
3
2,700,000
1
5/60
225,000
800
1
5/60
67
245,310
1
15/60
61,328
43,290
1
15/60
10,823
1,400
1
15/60
350
20
1
15/60
5
E:\FR\FM\17JNN1.SGM
17JNN1
34647
Federal Register / Vol. 80, No. 116 / Wednesday, June 17, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
(in hours)
Total burden
hours
Type of respondent
Form name/CFR reference
Importer/Filer .....................................
CDC PGA Message Set for Importing Cats and Dogs.
71.52(d) Turtle Importation Permits
(no form, just written request).
71.56(a)(2) African Rodents—Request for exemption ( no form,
written request only).
CDC PGA Message Set for Importing African Rodents.
71.55 Dead bodies (death certificates submitted).
71.56(a)(iii) Appeal (no form, written
request only).
Statement or documentation of Noninfectiousness (Documented, no
form; authority under 71.32(b)).
CDC PGA Message Set for Importing African Rodent and All Family
Viverridae Products.
30,000
1
15/60
7,500
5
1
30/60
3
20
1
1
20
60
1
15/60
15
5
1
1
5
2
1
1
2
2,000
1
5/60
167
2,000
1
15/60
500
...........................................................
........................
........................
........................
307,613
Importer .............................................
Importer .............................................
Importer/Filer .....................................
Importers ...........................................
Filer ...................................................
Filer/Importer .....................................
Importer/Filer .....................................
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. 2015–14787 Filed 6–16–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995 (the
PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
asabaliauskas on DSK5VPTVN1PROD with NOTICES
VerDate Sep<11>2014
18:47 Jun 16, 2015
Jkt 235001
Comments must be received by
August 17, 2015:
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
DATES:
[Document Identifier: CMS–10565]
SUMMARY:
any of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
Reports Clearance Office at (410) 786–
1326.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10565 Off-Cycle Submission of
Summaries of Model of Care Changes
Under the 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.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
E:\FR\FM\17JNN1.SGM
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]]>Agencies
[Federal Register Volume 80, Number 116 (Wednesday, June 17, 2015)]
[Notices]
[Pages 34645-34647]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-14787]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60-Day-15-0134; Docket No. CDC-2015-0039]
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 a revision to
several of the information collections pertaining to the importation of
dogs as outlined in the currently approved information collection
entitled ``Foreign Quarantine Regulations (42 CFR part 71)''.
DATES: Written comments must be received on or before August 17, 2015.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2015-
0039 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: 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
[[Page 34646]]
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
Foreign Quarantine Regulations (42 CFR part 71)--Revision--(OMB
Control No. 0920-0134, Expires September 30, 2017), National Center for
Emerging and Zoonotic Infections Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
This information collection revision request is an effort to
provide greater clarity surrounding paperwork requirements and focuses
exclusively on certain information collections that pertain to
importation of dogs into the United States. Specifically, CDC seeks to
make the following changes:
CDC is asking to correct a transcription error in the
burden tables in section 12. Currently, the relevant IC reads:
71.51(b)(2) Dogs/cats: Certification of Confinement, Vaccination (CDC
form 75.37). It should have been: 71.51(c)(2) Dogs: Certification of
Confinement, Vaccination (CDC form 75.37).
CDC is also proposing to replace the CDC form 75.37 NOTICE
TO OWNERS AND IMPORTERS OF DOGS: Requirement for Dog Confinement with a
new Application For Permission To Import A Dog Unimmunized Against
Rabies, which, if the importer meets the criteria for importation, will
be followed by a CDC-completed Permit to Conditionally Import a Dog
Inadequately Immunized against Rabies--Single Entry
CDC is also requesting approval to change and split the
current information collection (IC) ``71.51(c)(2) Dogs/cats:
Certification of Confinement, Vaccination (CDC form 75.37)'' into two
separate ICs.
CDC will include one modified IC: ``71.51(c)(2), (d)
Application For Permission To Import A Dog Unimmunized Against
Rabies''. This will include a reduced estimate of the numbers of these
permits, formerly CDC form 75.37 NOTICE TO OWNERS AND IMPORTERS OF
DOGS: Requirement for Dog Confinement, issued each year.
CDC will include a separate IC pertaining to 71.51(c)(1),
(d). The title for this IC is Valid Rabies Vaccination Certificate,
which will include only the burden associated with rabies vaccination
certificates.
CDC is also including an information collection for
71.51(c)(i), (ii), and (iii) which provides exemption criteria for the
importation of a dog without a rabies vaccination certificate.
CDC is not requesting changes to any of the other information
collections included under OMB control number 0920-0134.
The total requested burden hours is 307,613. There is no burden to
respondents other than the time taken to complete the reports or
documentation for CDC.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Form name/CFR Number of Number of burden per Total burden
Type of respondent reference respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Maritime conveyance operators. 71.21(a) Radio 2,000 1 2/60 67
Report of death/
illness--illnes
s reports from
ships (fillable
PDF (individual
case and
cumulative
report), phone,
transcribed
email).
Aircraft commander or 71.21(b) Death/ 1,700 1 2/60 57
operators. Illness reports
from aircrafts
(verbal, no
form).
Maritime conveyance operators. 71.21(c) 17,000 1 3/60 850
Gastrointestina
l Illnesses
reports 24 and
4 hours before
arrival (MIDRS).
Maritime conveyance operators. 71.21(c) 17,000 1 3/60 850
Recordkeeping--
Medical logs
(no form,
captains
provide logs).
Isolated or Quarantined 71.33(c) Report 11 1 3/60 1
individuals. by persons in
isolation or
surveillance
(verbal, no
form).
Maritime conveyance operators. 71.35 Report of 5 1 30/60 3
death/illness
during stay in
port (verbal,
no form).
Traveler...................... Locator Form 2,700,000 1 5/60 225,000
used in an
outbreak of
public health
significance.
Traveler...................... Locator Form 800 1 5/60 67
used for
reporting of an
ill
passenger(s).
Importer...................... 71.51(c)(1), 245,310 1 15/60 61,328
(d)--Valid
Rabies
Vaccination
Certificates.
Importer...................... 71.51(c)(i), 43,290 1 15/60 10,823
(ii), and (iii)
exemption
criteria for
the importation
of a dog
without a
rabies
vaccination
certificate.
Importer...................... 71.51(c)(2), (d) 1,400 1 15/60 350
Application For
Permission To
Import A Dog
Unimmunized
Against Rabies.
Importer...................... 71.51(b) (3) 20 1 15/60 5
Dogs/cats:
Record of
sickness or
deaths (no
form, record
review).
[[Page 34647]]
Importer/Filer................ CDC PGA Message 30,000 1 15/60 7,500
Set for
Importing Cats
and Dogs.
Importer...................... 71.52(d) Turtle 5 1 30/60 3
Importation
Permits (no
form, just
written
request).
Importer...................... 71.56(a)(2) 20 1 1 20
African
Rodents--Reques
t for exemption
( no form,
written request
only).
Importer/Filer................ CDC PGA Message 60 1 15/60 15
Set for
Importing
African Rodents.
Importers..................... 71.55 Dead 5 1 1 5
bodies (death
certificates
submitted).
Filer......................... 71.56(a)(iii) 2 1 1 2
Appeal (no
form, written
request only).
Filer/Importer................ Statement or 2,000 1 5/60 167
documentation
of Non-
infectiousness
(Documented, no
form; authority
under 71.32(b)).
Importer/Filer................ CDC PGA Message 2,000 1 15/60 500
Set for
Importing
African Rodent
and All Family
Viverridae
Products.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 307,613
----------------------------------------------------------------------------------------------------------------
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. 2015-14787 Filed 6-16-15; 8:45 am]
BILLING CODE 4163-18-P
