Proposed Data Collections Submitted for Public Comment and Recommendations, 75155-75157 [2014-29503]
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Federal Register / Vol. 79, No. 242 / Wednesday, December 17, 2014 / Notices
Counterparty Credit Risk Schedule
Significant additions would be made
to the Counterparty Credit Risk
Schedule in order to more adequately
and accurately capture exposure
information related to derivatives and
securities financing transactions
(‘‘SFTs’’). These additions would
remediate deficiencies discovered in the
current collection related to exposure,
including a lack of information
regarding collateral, asset types, and
total exposure to a given counterparty,
and have been carefully evaluated
internally and vetted with respondents.
The FDIC proposes: (1) Adding a subschedule that collects the derivative
exposures at a legal-entity nettingagreement level for the top 25 noncentral clearing counterparty (‘‘nonCCP’’) and non-G–7 counterparties, as
well as all CCPs and the G–7
counterparties, that includes a breakout
of collateral into cash and non-cash, and
exposures into 14 asset categories; (2)
changing the current SFT sub-schedule
to collect exposures and collateral
separately at a counterparty legal-entity
netting-agreement level for the top 25
non-CCP and non-G–7 counterparties, as
well as all CCPs and the G–7
counterparties, and adding asset subcategories for a total of 30 specific asset
types; (3) removing all columns with the
institution specification of margin
period of risk (‘‘MPOR’’) under the
global market shocks from subschedules F.1.a through F.1.e and F.2;
(4) removing the column LGD Derived
from Unstressed PD on F.2; and (5)
adding columns to worksheet F.1.e to
collect both gross and net stressed and
unstressed current exposure to central
clearing counterparties.
Burden Estimates
The FDIC estimates the burden of this
collection as follows:
mstockstill on DSK4VPTVN1PROD with NOTICES
Current
Number of Respondents: 4.
Annual Burden per Respondent:
1,040.
Total Annual Burden: 4,160.
Proposed
Estimated Number of Respondents: 4.
Annual Burden per Respondent:
1,040.
Estimated Total Annual Burden:
4,160 hours.
The FDIC recognizes that the Board
has estimated 88,401 hours for bank
holding companies to prepare the
Summary, Macroscenario, Operational
risk, Regulatory capital transitions,
Regulatory capital instruments, and
Counterparty credit risk schedules
submitted for the FR Y–14A. The FDIC
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19:49 Dec 16, 2014
Jkt 235001
believes that the systems covered
institutions use to prepare the FR Y–
14A reporting templates will also be
used to prepare the reporting templates
described in this notice. Comments
continue to be invited on:
(a) Whether the collection of
information is necessary for the proper
performance of the functions of the
FDIC, including whether the
information has practical utility;
(b) The accuracy of the FDIC’s
estimate of the burden of the 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 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.
Dated at Washington, DC, this 11th day of
December.
Robert E. Feldman,
Executive Secretary, Federal Deposit
Insurance Corporation.
[FR Doc. 2014–29418 Filed 12–16–14; 8:45 am]
BILLING CODE 6714–01–P
75155
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than January 12,
2015.
A. Federal Reserve Bank of Chicago
(Colette A. Fried, Assistant Vice
President) 230 South LaSalle Street,
Chicago, Illinois 60690–1414:
1. Brookfield Financial Holdings, Inc.,
Brookfield, Illinois; to become a bank
holding company by acquiring 100
percent of the voting shares of First
National Bank of Brookfield, Brookfield,
Illinois.
B. Federal Reserve Bank of
Minneapolis (Jacquelyn K. Brunmeier,
Assistant Vice President) 90 Hennepin
Avenue, Minneapolis, Minnesota
55480–0291:
1. Border Bancshares Inc., Greenbush,
Minnesota; to acquire 100 percent of the
voting shares of First Advantage Bank,
Coon Rapids, Minnesota.
2. Park Financial Group, Inc.,
Minneapolis, Minnesota; to become a
bank holding company by acquiring 100
percent of the voting shares of Park
State Bank, Duluth, Minnesota.
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
Board of Governors of the Federal Reserve
System, December 12, 2014.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
[FR Doc. 2014–29521 Filed 12–16–14; 8:45 am]
BILLING CODE 6210–01–P
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
PO 00000
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Fmt 4703
Sfmt 4703
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–15–0932]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC), as part of its
continuing effort 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. To request more
information on the below proposed
project or to obtain a copy of the
information collection plan and
instruments, call 404–639–7570 or send
comments to Leroy A. Richardson, 1600
E:\FR\FM\17DEN1.SGM
17DEN1
75156
Federal Register / Vol. 79, No. 242 / Wednesday, December 17, 2014 / Notices
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
Comments submitted in response to
this notice will be summarized and/or
included in the request for Office of
Management and Budget (OMB)
approval. 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. Written comments should
be received within 60 days of this
notice.
Proposed Project
Data Collection for Evaluation of
Education, Communication, and
Training Activities—Revision—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
medical exam technical instructions
more accessible.
Approval of this revision of the
generic information collection will
allow DGMQ continue to collect in an
expedited manner information about the
knowledge, attitudes, and behaviors of
key audiences (such as refugees,
immigrants, migrants, international
travelers, travel industry partners,
healthcare providers, non-profit
agencies, customs brokers and
forwarders, schools, state and local
health departments) to help improve
and inform these activities during both
routine and emergency public health
events. This generic OMB clearance will
help DGMQ continue to refine these
efforts in a timely manner, and will be
especially valuable for communication
activities that must occur quickly in
response to public health emergencies.
DGMQ staff will use a variety of data
collection methods for this proposed
project: Interviews, focus groups,
surveys, and pre/post-tests. Depending
on the research questions and audiences
involved, data may be gathered inperson, by telephone, online, or using
some combination of these formats. Data
may be collected in quantitative and/or
qualitative forms. Numerous audience
variables will be assessed under the
auspices of this generic OMB clearance.
These include, but are not limited to,
knowledge, attitudes, beliefs, behavioral
intentions, practices, behaviors, skills,
self-efficacy, and information needs and
sources. Insights gained from evaluation
research will assist in the development,
refinement, implementation, and
demonstration of outcomes and impact
of communication, education, and
training activities.
DGMQ estimates that 17,500
respondents and 7,982 hours of burden
will be involved in evaluation research
activities each year. The information
being collected will not impose a cost
burden on the respondents beyond that
associated with their time to provide the
required data.
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) Division of Global
Migration and Quarantine (DGMQ) is
requesting a revision of a currently
approved generic clearance to conduct
evaluation research. This will help CDC
plan and implement health
communication, education, and training
activities to improve health and prevent
the spread of disease. These activities
include communicating with
international travelers and other mobile
populations, training healthcare
providers, and educating public health
departments and other federal partners.
The information collection for which
the revision is sought is in accordance
with DGMQ’s mission to reduce
morbidity and mortality among
immigrants, refugees, travelers,
expatriates, and other globally mobile
populations, and to prevent the
introduction, transmission, or spread of
communicable diseases from foreign
countries into the United States. This
mission is supported by delegated legal
authorities outlined in the Public Health
Service (PHS) Act (42 U.S.C. 264) and
in regulations that are codified in 42
Code of Federal Regulations (CFR) parts
70 and 71, and 34.
Since receiving initial approval for
this generic, CDC has conducted three
information collections. These
information collections were in support
of an Evaluation of Adapted Health
Education Materials for LEP Spanish
Speakers and Indigenous Migrants;
Evaluation of the TravAlert Electronic
Messaging System; and, a project
entitled Scan This: Effectiveness of
Quick Response Codes for Engaging
International Panel Physicians. In order,
these projects evaluated materials
designed for specific audiences to
determine if CDC’s methods for
communicating key public health
messages were translated appropriately
for low-English proficiency residents in
the United States, were effective in
reaching travelers in airports, and were
useful in making CDC’s immigration
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
mstockstill on DSK4VPTVN1PROD with NOTICES
Type of respondents
Form name
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals Interviews
General Public ..................................
Focus Groups Screening form .........
Focus Groups Screening form .........
Focus Groups ...................................
Focus Groups ...................................
Interview Screening Form ................
Interview Screening Form ................
Interviews .........................................
Interviews .........................................
Survey Screening Forms .................
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19:49 Dec 16, 2014
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PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1,050
450
525
225
700
300
350
150
5,250
E:\FR\FM\17DEN1.SGM
1
1
1
1
1
1
1
1
1
17DEN1
Average
burden per
response
(in hours)
10/60
10/60
90/60
90/60
10/60
10/60
1
1
10/60
Total burden
(in hours)
175
75
788
338
117
50
350
150
875
75157
Federal Register / Vol. 79, No. 242 / Wednesday, December 17, 2014 / 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
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
General Public ..................................
Healthcare Professionals ..................
Survey Screening Forms .................
Surveys ............................................
Surveys ............................................
Pre/Post Tests ..................................
Pre/Post Tests ..................................
2,250
2,625
1,125
1,750
750
1
1
1
1
1
10/60
45/60
45/60
45/60
45/60
375
1,969
844
1,313
563
TOTAL .......................................
...........................................................
17,500
........................
........................
7,982
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. 2014–29503 Filed 12–16–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Office for State, Tribal, Local and
Territorial Support (OSTLTS) Meeting
mstockstill on DSK4VPTVN1PROD with NOTICES
In accordance with Presidential
Executive Order No. 13175, November
6, 2000, and the Presidential
Memorandum of November 5, 2009, and
September 23, 2004, Consultation and
Coordination with Indian Tribal
Governments, CDC/Agency for Toxic
Substances and Disease Registry
(ATSDR), announces the following
meeting and Tribal Consultation
Session:
Name: Tribal Advisory Committee (TAC)
Meeting and 12th Biannual Tribal
Consultation Session
Times and Dates:
8:00 a.m.–5:00 p.m., February 10, 2015 (TAC
Meeting)
8:00 a.m.–5:00 p.m., February 11, 2015 (12th
Biannual Tribal Consultation Session)
Place: The TAC Meeting and Tribal
Consultation Session will be held at CDC
Headquarters, 1600 Clifton Road, NE., Global
Communications Center, Auditorium B3,
Atlanta, Georgia 30333.
Status: The meetings are being hosted by
CDC/ATSDR in-person only and are open to
the public. Attendees must pre-register for
the event by Friday, January 23, 2015, at the
following link: https://www.cdc.gov/tribal/
meetings.html.
Purpose: The purpose of these recurring
meetings is to advance CDC/ATSDR support
for and collaboration with tribes, and to
improve the health of tribes through,
including but not limited to, assisting in
eliminating the health disparities faced by
Indian Tribes, ensuring that access to critical
health and human services and public health
VerDate Sep<11>2014
19:49 Dec 16, 2014
Jkt 235001
services is maximized to advance or enhance
the social, physical, and economic status of
Indians; and promoting health equity for all
Indian people and communities. To advance
these goals, CDC/ATSDR conducts
government-to-government consultations
with elected tribal officials or their
authorized representatives. Consultation is
an enhanced form of communication that
emphasizes trust, respect, and shared
responsibility. It is an open and free
exchange of information and opinion among
parties that leads to mutual understanding
and comprehension.
Matters for Discussion: The TAC and CDC
leaders will discuss the following public
health issue topics: Native specimens, injury
prevention and occupational safety, hepatitis
C virus, tuberculosis, and communication
and engagement with tribes; however,
discussion is not limited to these topics.
During the 12th Biannual Tribal
Consultation Session, tribes and CDC leaders
will engage in a listening session with CDC’s
director and roundtable discussions with
CDC senior leaders, and tribes will have an
opportunity to present testimony on tribal
health issues.
Tribal leaders are encouraged to submit
written testimony by January 23, 2015, to
April R. Taylor, Public Health Analyst for the
Tribal Support Unit, OSTLTS, via mail to
4770 Buford Highway NE., MS E–70, Atlanta,
Georgia 30341 or email to TribalSupport@
cdc.gov.
Depending on the time available, it may be
necessary to limit the time of each presenter.
The agenda is subject to change as
priorities dictate.
Information about the TAC, CDC’s Tribal
Consultation Policy, and previous meetings
can be found at the following web link:
https://www.cdc.gov/tribal.
Contact person for more information: April
R. Taylor, Public Health Analyst, CDC/
OSTLTS, 4770 Buford Highway NE., MS E–
70, Atlanta, Georgia 30341; email: ARTaylor@
cdc.gov.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Prevention, and the Agency for Toxic
Substances and Disease Registry.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2014–29489 Filed 12–16–14; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
The meeting announced below
concerns Occupational Safety and
Health Training Project Grants, PAR10–
288, initial review.
In accordance with Section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the aforementioned meeting:
Times and Dates:
6:00 p.m.–8:00 p.m., January 13, 2015
(Closed)
8:00 a.m.–8:00 p.m., January 14, 2015
(Closed)
Place: Atlanta Airport Marriott, 4711 Best
Road, Atlanta, Georgia 30337, Telephone:
(404) 766–7900
Status: The meeting will be closed to the
public in accordance with provisions set
forth in Section 552b(c) (4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters for Discussion: The meeting will
include the initial review, discussion, and
evaluation of applications received in
response to ‘‘Occupational Safety and Health
Training Project Grants, PAR10–288, initial
review.’’
Contact Person for More Information:
Donald Blackman, Ph.D., Scientific Review
Officer, CDC, 2400 Century Center Parkway,
NE., 4th Floor, Room 4204, Mailstop E–74,
Atlanta, Georgia 30345, Telephone: (404)
498–6185, DYB7@CDC.GOV.
The Director, Management Analysis and
Services Office, has been delegated the
E:\FR\FM\17DEN1.SGM
17DEN1
]]>Agencies
[Federal Register Volume 79, Number 242 (Wednesday, December 17, 2014)]
[Notices]
[Pages 75155-75157]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2014-29503]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-15-0932]
Proposed Data Collections Submitted for Public Comment and
Recommendations
The Centers for Disease Control and Prevention (CDC), as part of
its continuing effort 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. To request more information on the below
proposed project or to obtain a copy of the information collection plan
and instruments, call 404-639-7570 or send comments to Leroy A.
Richardson, 1600
[[Page 75156]]
Clifton Road, MS-D74, Atlanta, GA 30333 or send an email to
omb@cdc.gov.
Comments submitted in response to this notice will be summarized
and/or included in the request for Office of Management and Budget
(OMB) approval. 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. Written comments should be received within 60
days of this notice.
Proposed Project
Data Collection for Evaluation of Education, Communication, and
Training Activities--Revision--National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) Division of
Global Migration and Quarantine (DGMQ) is requesting a revision of a
currently approved generic clearance to conduct evaluation research.
This will help CDC plan and implement health communication, education,
and training activities to improve health and prevent the spread of
disease. These activities include communicating with international
travelers and other mobile populations, training healthcare providers,
and educating public health departments and other federal partners.
The information collection for which the revision is sought is in
accordance with DGMQ's mission to reduce morbidity and mortality among
immigrants, refugees, travelers, expatriates, and other globally mobile
populations, and to prevent the introduction, transmission, or spread
of communicable diseases from foreign countries into the United States.
This mission is supported by delegated legal authorities outlined in
the Public Health Service (PHS) Act (42 U.S.C. 264) and in regulations
that are codified in 42 Code of Federal Regulations (CFR) parts 70 and
71, and 34.
Since receiving initial approval for this generic, CDC has
conducted three information collections. These information collections
were in support of an Evaluation of Adapted Health Education Materials
for LEP Spanish Speakers and Indigenous Migrants; Evaluation of the
TravAlert Electronic Messaging System; and, a project entitled Scan
This: Effectiveness of Quick Response Codes for Engaging International
Panel Physicians. In order, these projects evaluated materials designed
for specific audiences to determine if CDC's methods for communicating
key public health messages were translated appropriately for low-
English proficiency residents in the United States, were effective in
reaching travelers in airports, and were useful in making CDC's
immigration medical exam technical instructions more accessible.
Approval of this revision of the generic information collection
will allow DGMQ continue to collect in an expedited manner information
about the knowledge, attitudes, and behaviors of key audiences (such as
refugees, immigrants, migrants, international travelers, travel
industry partners, healthcare providers, non-profit agencies, customs
brokers and forwarders, schools, state and local health departments) to
help improve and inform these activities during both routine and
emergency public health events. This generic OMB clearance will help
DGMQ continue to refine these efforts in a timely manner, and will be
especially valuable for communication activities that must occur
quickly in response to public health emergencies.
DGMQ staff will use a variety of data collection methods for this
proposed project: Interviews, focus groups, surveys, and pre/post-
tests. Depending on the research questions and audiences involved, data
may be gathered in-person, by telephone, online, or using some
combination of these formats. Data may be collected in quantitative
and/or qualitative forms. Numerous audience variables will be assessed
under the auspices of this generic OMB clearance. These include, but
are not limited to, knowledge, attitudes, beliefs, behavioral
intentions, practices, behaviors, skills, self-efficacy, and
information needs and sources. Insights gained from evaluation research
will assist in the development, refinement, implementation, and
demonstration of outcomes and impact of communication, education, and
training activities.
DGMQ estimates that 17,500 respondents and 7,982 hours of burden
will be involved in evaluation research activities each year. The
information being collected will not impose a cost burden on the
respondents beyond that associated with their time to provide the
required data.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondents Form name respondents responses per response (in (in hours)
respondent hours)
----------------------------------------------------------------------------------------------------------------
General Public................ Focus Groups 1,050 1 10/60 175
Screening form.
Healthcare Professionals...... Focus Groups 450 1 10/60 75
Screening form.
General Public................ Focus Groups.... 525 1 90/60 788
Healthcare Professionals...... Focus Groups.... 225 1 90/60 338
General Public................ Interview 700 1 10/60 117
Screening Form.
Healthcare Professionals...... Interview 300 1 10/60 50
Screening Form.
General Public................ Interviews...... 350 1 1 350
Healthcare Professionals Interviews...... 150 1 1 150
Interviews.
General Public................ Survey Screening 5,250 1 10/60 875
Forms.
[[Page 75157]]
Healthcare Professionals...... Survey Screening 2,250 1 10/60 375
Forms.
General Public................ Surveys......... 2,625 1 45/60 1,969
Healthcare Professionals...... Surveys......... 1,125 1 45/60 844
General Public................ Pre/Post Tests.. 1,750 1 45/60 1,313
Healthcare Professionals...... Pre/Post Tests.. 750 1 45/60 563
---------------------------------------------------------------
TOTAL..................... ................ 17,500 .............. .............. 7,982
----------------------------------------------------------------------------------------------------------------
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. 2014-29503 Filed 12-16-14; 8:45 am]
BILLING CODE 4163-18-P
