60 Day FRN

tkelley on DSK3SPTVN1PROD with NOTICES

Federal Register / Vol. 80, No. 87 / Wednesday, May 6, 2015 / Notices
controlled non-U.S. branch. The FFIEC
002S must be filed quarterly along with
the U.S. branch or agency’s FFIEC 002.
The data from both reports are used for
(1) monitoring deposit and credit
transactions of U.S. residents; (2)
monitoring the impact of policy
changes; (3) analyzing structural issues
concerning foreign bank activity in U.S.
markets; (4) understanding flows of
banking funds and indebtedness of
developing countries in connection with
data collected by the International
Monetary Fund and the Bank for
International Settlements that are used
in economic analysis; and (5) assisting
in the supervision of U.S. offices of
foreign banks. The Federal Reserve
System collects and processes these
reports on behalf of all three agencies.
No changes are proposed to the FFIEC
002 and FFIEC 002S reporting forms or
instructions.
2. Report title: Country Exposure
Report for U.S. Branches and Agencies
of Foreign Banks.
Agency form number: FFIEC 019.
OMB control number: 7100–0213.
Frequency of response: Quarterly.
Affected public: U.S. branches and
agencies of foreign banks.
Number of respondents: 167.
Estimated average time per response:
10 hours.
Estimated total annual burden: 6,680
hours.
General description of report: This
information collection is mandatory (12
U.S.C. 3906 for all agencies); 12 U.S.C.
3105 and 3108 for the Board; 12 U.S.C.
1817 and 1820 for the FDIC; and 12
U.S.C. 161 for the OCC. This
information collection is given
confidential treatment under the
Freedom of Information Act (5 U.S.C.
552(b)(8)).
Abstract: All individual U.S. branches
and agencies of foreign banks that have
more than $30 million in direct claims
on residents of foreign countries must
file the FFIEC 019 report quarterly.
Currently, all respondents report
adjusted exposure amounts to the five
largest countries having at least $20
million in total adjusted exposure. The
agencies collect this data to monitor the
extent to which such branches and
agencies are pursuing prudent country
risk diversification policies and limiting
potential liquidity pressures. No
changes are proposed to the FFIEC 019
reporting form or instructions.
Request for Comment
Comments are invited on:
a. Whether the information
collections are necessary for the proper
performance of the agencies’ functions,

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18:43 May 05, 2015

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including whether the information has
practical utility;
b. The accuracy of the agencies’
estimate of the burden of the
information collections, including the
validity of the methodology and
assumptions used;
c. Ways to enhance the quality,
utility, and clarity of the information to
be collected;
d. Ways to minimize the burden of the
information collections 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.
Comments submitted in response to
this notice will be shared among the
agencies. All comments will become a
matter of public record.

26051

laboratories; infection control
professionals; and healthcare providers.
EIPs assist in local, state, and national
efforts to prevent, control, and monitor
the public health impact of infectious
diseases through population-based
surveillance.

BILLING CODE 6210–01–P

Written comments must be
received on or before July 6, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0030 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.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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.

Board of Governors of the Federal Reserve
System, May 1, 2015.
Robert deV. Frierson,
Secretary of the Board.
[FR Doc. 2015–10600 Filed 5–5–15; 8:45 am]

Centers for Disease Control and
Prevention
[60-Day–15–0978; Docket No. CDC–2015–
0030]

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 the proposed information
collection for the Emerging Infections
Program. The Emerging Infections
Programs (EIPs) are population-based
centers of excellence established
through a network of state health
departments collaborating with
academic institutions; local health
departments; public health and clinical

SUMMARY:

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DATES:

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

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26052

Federal Register / Vol. 80, No. 87 / Wednesday, May 6, 2015 / Notices

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.

Activities of the EIPs fall into the
following general categories: (1) Active
surveillance; (2) applied public health
epidemiologic and laboratory activities;
(3) implementation and evaluation of
pilot prevention/intervention projects;
and (4) flexible response to public
health emergencies.
Activities of the EIPs are designed to:
(1) Address issues that the EIP network
is particularly suited to investigate; (2)
maintain sufficient flexibility for
emergency response and new problems
as they arise; (3) develop and evaluate
public health interventions to inform
public health policy and treatment
guidelines; (4) incorporate training as a
key function; and (5) prioritize projects
that lead directly to the prevention of
disease.
Proposed respondents will include
state health departments who may
collaborate with one or more of the
following: Academic institutions, local
health departments, public health and
clinical laboratories, infection control
professionals, and healthcare providers.
Frequency of reporting will be
determined as cases arise.
The total estimated burden is 22,755
hours. There is no cost to respondents
other than their time.

Proposed Project
Emerging Infections Program—(OMB
Control No. 0920–0978, Expires 8/31/
2016)—Revision—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Emerging Infections Programs
(EIPs) are population-based centers of
excellence established through a
network of state health departments
collaborating with academic
institutions; local health departments;
public health and clinical laboratories;
infection control professionals; and
healthcare providers. EIPs assist in
local, state, and national efforts to
prevent, control, and monitor the public
health impact of infectious diseases.
Various parts of the EIP have received
separate Office of Management and
Budget (OMB) clearances (Active
Bacterial Core Surveillance [ABCs]—
OMB number 0920–0802 and All Age
Influenza Hospitalization
Surveillance—OMB number 0920–
0852); however this request seeks to
have all core EIP activities under one
clearance.

tkelley on DSK3SPTVN1PROD with NOTICES

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents

Type of respondent

Form name

State Health Department

ABCs Case Report Form ....................................
Invasive Methicillin-resistant Staphylococcus
aureus ABCs Case Report Form.
ABCs Invasive Pneumococcal Disease in Children Case Report Form.
ABCs Non-Bacteremic Pneumococcal Disease
Case Report Form.
Neonatal Infection Expanded Tracking Form ......
ABCs Legionellosis Case Report Form ..............
Campylobacter .....................................................
Cryptosporidium ...................................................
Cyclospora ...........................................................
Listeria monocytogenes .......................................
Salmonella ...........................................................
Shiga toxin producing E. coli ...............................
Shigella ................................................................
Vibrio ....................................................................
Yersinia ................................................................
Hemolytic Uremic Syndrome ...............................
Influenza Hospitalization Surveillance Project
Case Report Form.
Influenza Hospitalization Surveillance Project
Vaccination Telephone Survey.
Influenza Hospitalization Surveillance Project
Vaccination Telephone Survey Consent Form.
CDI Case Report Form .......................................
CDI Treatment Form ...........................................
Resistant Gram-Negative Bacilli Case Report
Form.
Screening Form ...................................................

EIP site ..........................

Person in the community
infected with C.
difficile (CDI Cases).

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Number of
responses per
respondent

Average
burden per
response
(in hours)

Total burden
(in hours)

10
10

809
609

20/60
20/60

2,697
2,030

10

22

10/60

37

10

100

10/60

167

10
10
10
10
10
10
10
10
10
10
10
10
10

37
100
637
130
3
13
827
90
178
20
16
10
400

20/60
20/60
20/60
10/60
10/60
20/60
20/60
20/60
10/60
10/60
10/60
1
15/60

123
333
2,123
217
5
43
2,757
300
297
33
27
100
1,000

10

100

5/60

83

10

100

5/60

83v

10
10
10

1,650
1,650
500

20/60
10/60
20/60

5,500
2,750
1,667

600

1

5/60

50

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26053

Federal Register / Vol. 80, No. 87 / Wednesday, May 6, 2015 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Type of respondent

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

500

1

40/60

333

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

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

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

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

22,728

[FR Doc. 2015–10543 Filed 5–5–15; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–15AEP; Docket No. CDC–2015–
0029]

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 two information
collections titled ‘‘Persistence of Ebola
Virus in Body Fluids of Ebola Virus
Disease (EVD) Survivors in Sierra
Leone’’ and ‘‘Assessment of Public
Knowledge, Attitudes, and Practices
(KAPs) Relating to EVD Prevention and
Medical Care in Guinea.’’ The purpose
of these information collections is to
gather the necessary information for the
CDC and the international community
to begin the activities necessary to reach
the goal of zero new EVD cases
throughout West Africa. Once that goal
is reached, the 42-day countdown to
declare West Africa Ebola-free can
begin. Similar requests for public
comment will be published as new
information collections are proposed in

SUMMARY:

tkelley on DSK3SPTVN1PROD with NOTICES

Total burden
(in hours)

Telephone interview ............................................

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.

VerDate Sep<11>2014

Average
burden per
response
(in hours)

Number of
responses per
respondent

Number of
respondents

Form name

18:43 May 05, 2015

Jkt 235001

the effort to meet the international goal
of zero new EVD cases.
DATES: Written comments must be
received on or before July 6, 2015.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2015–
0029 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: [email protected].
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
FOR FURTHER INFORMATION CONTACT:

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Fmt 4703

Sfmt 4703

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 Projects
A Study of Viral Persistence in Ebola
Virus Disease (EVD) Survivors and an
Assessment of Public Knowledge,
Attitudes, and Practices Relating to EVD
Prevention and Medical Care—New—
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Much progress has been made in the
year since the CDC first responded to
the Ebola outbreak in West Africa, but
the agency’s efforts must continue until
there are zero new cases of Ebola virus
disease (EVD). As the CDC’s 2014 Ebola

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