Agency Forms Undergoing Paperwork Reduction Act Review, 36992-36993 [2015-15831]
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mstockstill on DSK4VPTVN1PROD with NOTICES
36992
Federal Register / Vol. 80, No. 124 / Monday, June 29, 2015 / Notices
Reporters: Individuals, households,
and financial and non-financial
businesses.
Estimated annual reporting hours:
Annual survey, 6,000 hours; Monthly
survey, 18,000 hours.
Estimated average hours per response:
Annual survey, 60 minutes; Monthly
survey, 30 minutes.
Number of respondents: Annual
survey, 6,000; Monthly survey, 3,000.
General description of report: This
information collection is voluntary and
is authorized by sections 2A and 12A of
the Federal Reserve Act (12 U.S.C. 225A
and 263). If needed, the Federal Reserve
can make this survey mandatory for
Federal Reserve regulated institutions
under section 9 of the Federal Reserve
Act (12 U.S.C. 324) for state member
banks; section 5(c) of the Bank Holding
Company Act (12 U.S.C. 1844(c)) for
bank holding companies and their
subsidiaries; sections 25 and 25(A) of
the Federal Reserve Act (12 U.S.C. 602
and 625) for Edge and agreement
corporations; and section 7(c)(2) of the
International Banking Act of 1978 (12
U.S.C. 3105(c)(2)) for U.S. branches and
agencies of foreign banks.
If the FR 3051 survey information is
collected with a pledge of
confidentiality for exclusively statistical
purposes under Confidential
Information Protection and Statistical
Efficiency Act (CIPSEA), the
information may not be disclosed by the
Federal Reserve (or its contractor) in
identifiable form, except with the
informed consent of the respondent
(CIPSEA 512(b), codified in notes to 44
U.S.C. 3501). Such information is
therefore protected from disclosure
under exemption 3 of the Freedom of
Information Act (FOIA) (5 U.S.C.
552(b)(3)). If a CIPSEA pledge is made,
either by the Federal Reserve or by its
contractor, the Federal Reserve must
safeguard the information as required by
CIPSEA and OMB guidance.
If the FR 3051 survey information is
not being collected under CIPSEA, the
ability of the Federal Reserve to
maintain the confidentiality of
information provided by respondents
will have to be determined on a case-bycase basis and depends on the type of
information provided for a particular
survey. In circumstances where
identifying information is provided to
the Federal Reserve, such information
could possibly be protected from
disclosure by FOIA exemptions 4 and 6.
Abstract: The Federal Reserve
implemented this event-driven survey
in 2009 and uses it to obtain
information specifically tailored to the
Federal Reserve’s supervisory,
regulatory, operational, and other
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17:13 Jun 26, 2015
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responsibilities. The Federal Reserve
can conduct the FR 3051 up to 13 times
per year (annual survey and another
survey on a monthly basis). The
frequency and content of the questions
depend on changing economic,
regulatory, or legislative developments.
3. Report title: Recordkeeping and
Disclosure Provisions associated with
Stress Testing Guidance.
Agency form number: FR 4202.
OMB control number: 7100–0348.
Frequency: On-occasion.
Reporters: State member banks, bank
holding companies, and all other
institutions for which the Federal
Reserve is the primary federal
supervisor.
Estimated annual reporting hours:
Recordkeeping, 18,000 hours;
Disclosure, 8,000 hours.
Estimated average hours per response:
Recordkeeping, 180 hours; Disclosure,
80 hours.
Number of respondents:
Recordkeeping, 100; Disclosure, 100.
General description of report: This
information collection is voluntary and
is authorized pursuant to sections 11(a),
11(i), 25, and 25A of the Federal Reserve
Act (12 U.S.C. 248(a), 248(i), 602, and
611), section 5 of the Bank Holding
Company Act (12 U.S.C. 1844), and
section 7(c) of the International Banking
Act (12 U.S.C. 3105(c)). To the extent
the Federal Reserve collects information
during an examination of a banking
organization, confidential treatment
may be afforded to the records under
exemptions 4 and 8 of the Freedom of
Information Act (FOIA) (5 U.S.C.
552(b)(4) and (8)).
Abstract: The interagency guidance
outlines high-level principles for stress
testing practices, applicable to all
Federal Reserve-supervised, FDICsupervised, and OCC-supervised
banking organizations 1 with more than
$10 billion in total consolidated assets.
In developing a stress testing framework
and in carrying out stress tests, banking
organizations 2 should understand and
clearly document all assumptions,
uncertainties, and limitations, and
provide that information to users of the
stress testing results. To ensure proper
governance over the stress testing
1 The agencies that were party to the rulemaking
were the Office of the Comptroller of the Currency
(OCC); Board of Governors of the Federal Reserve
System (Board); and Federal Deposit Insurance
Corporation (FDIC).
2 For purposes of this guidance, the term
‘‘banking organization’’ means national banks and
Federal branches and agencies supervised by the
OCC; state member banks, bank holding companies,
and all other institutions for which the Federal
Reserve is the primary federal supervisor; and state
nonmember insured banks and other institutions
supervised by the FDIC.
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Frm 00032
Fmt 4703
Sfmt 4703
framework, banking organizations
should develop and maintain written
policies and procedures.
Board of Governors of the Federal Reserve
System, June 24, 2015.
Robert deV. Frierson,
Secretary of the Board.
[FR Doc. 2015–15843 Filed 6–26–15; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–15PI]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
burden of the proposed collection of
information, including the validity of
the methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected; (d) Minimize the burden of
the collection of information on those
who are to respond, including through
the use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and (e) Assess information
collection costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Written
comments and/or suggestions regarding
the items contained in this notice
should be directed to the Attention:
CDC Desk Officer, Office of Management
and Budget, Washington, DC 20503 or
E:\FR\FM\29JNN1.SGM
29JNN1
36993
Federal Register / Vol. 80, No. 124 / Monday, June 29, 2015 / Notices
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
Extended Evaluation of the National
Tobacco Prevention and Control Public
Education Campaign—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2012, the Centers for Disease
Control and Prevention (CDC) launched
the first federally funded, national mass
media campaign to educate consumers
about the adverse health consequences
of tobacco use (the National Tobacco
Prevention and Control Public
Education Campaign, or ‘‘The
Campaign’’). The Campaign continued
in 2013 and 2014 with advertisements
known as ‘‘Tips From Former Smokers.’’
Activities for Phase 3 of the campaign
are ongoing. To assess the impact of The
Campaign in Phases 1–3, CDC obtained
OMB approval to conduct a series of
longitudinal surveys for smokers and
nonsmokers (OMB No. 0920–0923, exp.
3/31/2017).
New media activities for Phase 4 of
The Campaign launched in March 2015.
To support evaluation of Phase 4 of The
Campaign, CDC plans to field 4 new
waves of information collection. The
surveys will be fielded in English and
Spanish and will occur during late 2015
and throughout 2016. Once enrolled in
the first wave of data collection, all
participants will be re-contacted for
follow-up.
The sample for the data collection
will originate from two sources: (1) An
online longitudinal cohort of smokers
and nonsmokers, sampled randomly
from postal mailing addresses in the
United States (address-based sample, or
ABS); and (2) the existing GfK
KnowledgePanel, an established longterm online panel of U.S. adults. The
ABS-sourced longitudinal cohort will
consist of smokers and nonsmokers who
have not previously participated in any
established online panels to reduce
potential panel conditioning bias from
previous participation. The new cohort
will be recruited by GfK, utilizing
similar recruitment methods that are
used in the recruitment of
KnowledgePanel. The GfK
KnowledgePanel will be used in
combination with the new ABS-sourced
cohort to support larger sample sizes
that will allow for more in-depth
subgroup analysis, which is a key
objective for CDC. All online surveys,
regardless of sample source, will be
conducted via the GfK KnowledgePanel
Web portal for self-administered
surveys.
Information will be collected through
Web surveys to be self-administered on
computers in the respondent’s home or
in another convenient location.
Information will be collected about
smokers’ and nonsmokers’ awareness of
and exposure to specific campaign
advertisements; knowledge, attitudes,
beliefs related to smoking and
secondhand smoke; and other marketing
exposure. The surveys will also measure
behaviors related to smoking cessation
(among the smokers in the sample) and
behaviors related to nonsmokers’
encouragement of smokers to quit
smoking, recommendations of cessation
services, and attitudes about other
tobacco and nicotine products.
It is important to evaluate The
Campaign in a context that assesses the
dynamic nature of tobacco product
marketing and uptake of various tobacco
products, particularly since these may
affect successful cessation rates. Survey
instruments may be updated to include
new or revised items on relevant topics,
including cigars, noncombustible
tobacco products, and other emerging
trends in tobacco use.
Participation is voluntary and there
are no costs to respondents other than
their time. The total estimated
annualized burden hours are 15,584.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
General Population .........................................
Adults Smokers and Nonsmokers, ages 18–
54, in the United States.
Screening & Consent Questionnaire .............
Smoker Survey (Wave A) ..............................
Smoker Survey (Wave B) ..............................
Smoker Survey (Wave C) ..............................
Smoker Survey (Wave D) ..............................
Nonsmoker Survey (Wave A) ........................
Nonsmoker Survey (Wave B) ........................
Nonsmoker Survey (Wave C) ........................
Nonsmoker Survey (Wave D) ........................
Leroy 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.
mstockstill on DSK4VPTVN1PROD with NOTICES
[FR Doc. 2015–15831 Filed 6–26–15; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–15–15UX]
Agency Forms Undergoing Paperwork
Reduction Act Review
BILLING CODE 4163–18–P
The Centers for Disease Control and
Prevention (CDC) has submitted the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
VerDate Sep<11>2014
17:13 Jun 26, 2015
Jkt 235001
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
25,000
6,500
4,000
4,000
4,000
2,500
2,000
2,000
2,000
Number of
responses per
respondent
1
1
1
1
1
1
1
1
1
Average
burden per
response
(in hours)
5/60
30/60
30/60
30/60
30/60
30/60
30/60
30/60
30/60
Reduction Act of 1995. The notice for
the proposed information collection is
published to obtain comments from the
public and affected agencies.
Written comments and suggestions
from the public and affected agencies
concerning the proposed collection of
information are encouraged. Your
comments should address any of the
following: (a) Evaluate whether the
proposed collection of information is
necessary for the proper performance of
the functions of the agency, including
whether the information will have
practical utility; (b) Evaluate the
accuracy of the agencies estimate of the
E:\FR\FM\29JNN1.SGM
29JNN1
]]>Agencies
[Federal Register Volume 80, Number 124 (Monday, June 29, 2015)]
[Notices]
[Pages 36992-36993]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2015-15831]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-15-15PI]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) has submitted
the following information collection request to the Office of
Management and Budget (OMB) for review and approval in accordance with
the Paperwork Reduction Act of 1995. The notice for the proposed
information collection is published to obtain comments from the public
and affected agencies.
Written comments and suggestions from the public and affected
agencies concerning the proposed collection of information are
encouraged. Your comments should address any of the following: (a)
Evaluate whether the proposed collection of information is necessary
for the proper performance of the functions of the agency, including
whether the information will have practical utility; (b) Evaluate the
accuracy of the agencies estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used; (c) Enhance the quality, utility, and clarity of
the information to be collected; (d) Minimize the burden of the
collection of information on those who are to respond, including
through the use of appropriate automated, electronic, mechanical, or
other technological collection techniques or other forms of information
technology, e.g., permitting electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to omb@cdc.gov. Written comments and/or
suggestions regarding the items contained in this notice should be
directed to the Attention: CDC Desk Officer, Office of Management and
Budget, Washington, DC 20503 or
[[Page 36993]]
by fax to (202) 395-5806. Written comments should be received within 30
days of this notice.
Proposed Project
Extended Evaluation of the National Tobacco Prevention and Control
Public Education Campaign--New--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
In 2012, the Centers for Disease Control and Prevention (CDC)
launched the first federally funded, national mass media campaign to
educate consumers about the adverse health consequences of tobacco use
(the National Tobacco Prevention and Control Public Education Campaign,
or ``The Campaign''). The Campaign continued in 2013 and 2014 with
advertisements known as ``Tips From Former Smokers.'' Activities for
Phase 3 of the campaign are ongoing. To assess the impact of The
Campaign in Phases 1-3, CDC obtained OMB approval to conduct a series
of longitudinal surveys for smokers and nonsmokers (OMB No. 0920-0923,
exp. 3/31/2017).
New media activities for Phase 4 of The Campaign launched in March
2015. To support evaluation of Phase 4 of The Campaign, CDC plans to
field 4 new waves of information collection. The surveys will be
fielded in English and Spanish and will occur during late 2015 and
throughout 2016. Once enrolled in the first wave of data collection,
all participants will be re-contacted for follow-up.
The sample for the data collection will originate from two sources:
(1) An online longitudinal cohort of smokers and nonsmokers, sampled
randomly from postal mailing addresses in the United States (address-
based sample, or ABS); and (2) the existing GfK KnowledgePanel, an
established long-term online panel of U.S. adults. The ABS-sourced
longitudinal cohort will consist of smokers and nonsmokers who have not
previously participated in any established online panels to reduce
potential panel conditioning bias from previous participation. The new
cohort will be recruited by GfK, utilizing similar recruitment methods
that are used in the recruitment of KnowledgePanel. The GfK
KnowledgePanel will be used in combination with the new ABS-sourced
cohort to support larger sample sizes that will allow for more in-depth
subgroup analysis, which is a key objective for CDC. All online
surveys, regardless of sample source, will be conducted via the GfK
KnowledgePanel Web portal for self-administered surveys.
Information will be collected through Web surveys to be self-
administered on computers in the respondent's home or in another
convenient location. Information will be collected about smokers' and
nonsmokers' awareness of and exposure to specific campaign
advertisements; knowledge, attitudes, beliefs related to smoking and
secondhand smoke; and other marketing exposure. The surveys will also
measure behaviors related to smoking cessation (among the smokers in
the sample) and behaviors related to nonsmokers' encouragement of
smokers to quit smoking, recommendations of cessation services, and
attitudes about other tobacco and nicotine products.
It is important to evaluate The Campaign in a context that assesses
the dynamic nature of tobacco product marketing and uptake of various
tobacco products, particularly since these may affect successful
cessation rates. Survey instruments may be updated to include new or
revised items on relevant topics, including cigars, noncombustible
tobacco products, and other emerging trends in tobacco use.
Participation is voluntary and there are no costs to respondents
other than their time. The total estimated annualized burden hours are
15,584.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
General Population.................... Screening & Consent 25,000 1 5/60
Questionnaire.
Adults Smokers and Nonsmokers, ages 18- Smoker Survey (Wave A).. 6,500 1 30/60
54, in the United States. Smoker Survey (Wave B).. 4,000 1 30/60
Smoker Survey (Wave C).. 4,000 1 30/60
Smoker Survey (Wave D).. 4,000 1 30/60
Nonsmoker Survey (Wave 2,500 1 30/60
A).
Nonsmoker Survey (Wave 2,000 1 30/60
B).
Nonsmoker Survey (Wave 2,000 1 30/60
C).
Nonsmoker Survey (Wave 2,000 1 30/60
D).
----------------------------------------------------------------------------------------------------------------
Leroy 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. 2015-15831 Filed 6-26-15; 8:45 am]
BILLING CODE 4163-18-P
