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Federal Register / Vol. 81, No. 24 / Friday, February 5, 2016 / Notices

Frequency: On occasion.
Reporters: Banking organization,
including U.S. intermediate holding
companies (IHCs), with aggregate
trading assets and trading liabilities
equal to (1) 10 percent or more of
quarter-end total assets or (2) $1 billion
or more.
Estimated annual reporting hours:
Prior written approvals reporting:
28,800 hours; policies and procedures
recordkeeping: 2,880 hours; trading and
hedging strategy recordkeeping: 480
hours; internal models recordkeeping:
3,840 hours; section 4(b) backtesting
and stress testing: 1,920 hours; sections
5(c) and 9(c) backtesting and stress
testing: 3,120 hours; securitizations
backtesting and stress testing: 14,400
hours; disclosure policy backtesting and
stress testing: 1,200 hours; quantitative
disclosure: 1,920 hours; qualitative
disclosure: 360 hours.
Estimated average hours per response:
Prior written approvals reporting: 960
hours; policies and procedures
recordkeeping: 96 hours; trading and
hedging strategy recordkeeping: 16
hours; internal models recordkeeping:
128 hours; section 4(b) backtesting and
stress testing: 16 hours; sections 5(c)
and 9(c) backtesting and stress testing:
104 hours; securitizations backtesting
and stress testing: 120 hours; disclosure
policy backtesting and stress testing: 40
hours; quantitative disclosure: 16 hours;
qualitative disclosure: 12 hours.
Number of respondents: 30.
General description of report: This
information collection is mandatory
pursuant to 12 U.S.C. 324 and 12 U.S.C.
1844(c), section 165 of the Dodd-Frank
Act (12 U.S.C. 5365), and section
252.153(b)(2) of Regulation YY (12 CFR
252.153(b)(2)). Information collected
pursuant to the reporting requirements
of the FR 4201 (specifically, information
related to seeking regulatory approval
for the use of certain incremental and
comprehensive risk models and
methodologies under sections 217.208
and 217.209) is exempt from disclosure
pursuant to exemption (b)(8) of the
Freedom of Information Act (FOIA) (5
U.S.C § 552(b)(8)), and exemption (b)(4)
of FOIA (5 U.S.C. 552(b)(4)). Exemption
(b)(8) applies because the reported
information is contained in or related to
examination reports. Exemption (b)(4)
applies because the information
provided to obtain regulatory approval
of the incremental or comprehensive
risk models is confidential business
information the release of which could
cause substantial competitive harm to
the reporting company. The
recordkeeping requirements of the FR
4201 require banking organizations to
maintain documentation regarding

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certain policies and procedures, trading
and hedging strategies, and internal
models. These documents would remain
on the premises of the banking
organizations and accordingly would
not generally be subject to a FOIA
request. To the extent these documents
are provided to the regulators, they
would be exempt under exemption
(b)(8), and may be exempt under
exemption (b)(4). Exemption (b)(4)
protects from disclosure ‘‘trade secrets
and commercial or financial information
obtained from a person and privileged
or confidential.’’ The disclosure
requirements of the FR 4201 do not raise
any confidentiality issues because they
require banking organizations to make
certain disclosures public.
Abstract: The market risk rule is an
integral part of the Board’s regulatory
capital framework. The collection of
information permits the Federal Reserve
to monitor the market risk profile of
banking organizations that it regulates
and evaluate the impact and
competitive implications of the market
risk rule on those banking organizations
and the industry as a whole. The
collection of information provides the
most current statistical data available to
identify areas of market risk on which
to focus for onsite and offsite
examinations and allows the Federal
Reserve to assess and monitor the levels
and components of each reporting
institution’s risk-based capital
requirements for market risk and the
adequacy of the institution’s capital
under the market risk rule. Finally, the
collection of information contained in
the market risk rule is necessary to
ensure capital adequacy of banking
organizations according to their level of
market risk and assists banking
organizations in implementing and
validating the market risk framework.
Current Actions: The Federal Reserve
proposes to collect financial information
for U.S. Intermediate Holding
Companies (IHCs) of foreign banking
organizations (FBOs) for the regulatory
report forms listed above, beginning
with the reporting period ending on
September 30, 2016, to implement the
enhanced prudential standards for FBOs
adopted pursuant to Subparts L, M, N,
and O of Regulation YY to indicate and
to certify to the Federal Reserve Board
their compliance with those
requirements.
With regard to the FR Y–14 series of
reports, the IHC would be required to
complete the FR Y–14 reports in the
same manner as a BHC, and would be
subject to requirements to report
historical data with respect to its U.S.
bank and nonbank operations. The
reporting instructions provide IHCs

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with the submission dates for each of
the FR Y–14 reports, including the
onboarding filing delays that apply to
certain schedules, and the requirements
for reporting historical data for the FR
Y–14Q Retail and PPNR schedules. IHCs
will also receive this information in an
onboarding memo. The historical data
are necessary for the Board to perform
a supervisory assessment of the capital
plans of IHCs and to conduct
supervisory stress tests. The Federal
Reserve expects to address requirements
for the Market Shock exercise, as they
would apply to IHCs with significant
trading activity, in a separate proposal.
However, many IHCs may have
difficulty reporting historical data prior
to formation of the IHC because of the
structural reorganizations associated
with complying with the IHC
requirement. In addition, the ability of
IHCs to report historical data may differ
because compliance burdens may vary
in complexity across IHCs. The Federal
Reserve invites comment on the ability
of IHCs to report historical data,
including, but not limited to
• a description, with supporting
detail, of any challenges that IHCs may
face in providing historical data;
• specific compliance burdens for
IHCs, such as issues related to systems
integration or data retention policies;
and
• whether an IHC would be able to
report historical data if granted an
extension of time, and if so, how much
additional time would be needed.
Board of Governors of the Federal Reserve
System, February 2, 2016.
Robert deV. Frierson,
Secretary of the Board.
[FR Doc. 2016–02230 Filed 2–4–16; 8:45 am]
BILLING CODE 6210–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–16MM; Docket No. CDC–2016–
0019]

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

SUMMARY:

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Federal Register / Vol. 81, No. 24 / Friday, February 5, 2016 / Notices
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 proposed information
collection project entitled Performance
Monitoring of ‘‘Working with Publicly
Funded Health Centers to Reduce Teen
Pregnancy among Youth from
Vulnerable Populations.’’ CDC seeks to
collect information to monitor
performance of three awardees working
on teen pregnancy prevention project
and to determine training and technical
assistance needs to address any
performance issues.
DATES: Written comments must be
received on or before April 5, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0019 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.

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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: [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

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extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Performance Monitoring of ‘‘Working
with Publicly Funded Health Centers to
Reduce Teen Pregnancy among Youth
from Vulnerable Populations’’—New—
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
In 2014, the US rate of 24.2 births per
1,000 women aged 15–19 was the
highest of all Western industrialized
countries. Access to reproductive health
services and the most effective types of
contraception have been shown to
reduce the likelihood that teens become
pregnant. Nevertheless, reviews of
recent research and teen pregnancy
prevention projects, including a
collaborative project implemented by
CDC and the HHS Office of Adolescent

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Health (2010–2015), demonstrate that
many health centers serving adolescents
do not engage in youth-friendly best
practices that may enhance access to
care and to the most effective types of
contraception. Furthermore, youth at
highest risk of experiencing a teen
pregnancy are often not connected to
the reproductive health care that they
need, even when they are part of a
population that is known to be at high
risk for a teen pregnancy. Significant
racial, ethnic and geographic disparities
in teen birth rates persist and continue
to be a focus of public health efforts.
To address these challenges, CDC is
providing funding to three organizations
to strengthen partnerships and
processes that improve reproductive
health services for teens. CDC’s
awardees will work with approximately
35 publicly funded health centers to
implement organizational changes and
provider training based on best practices
in adolescent reproductive health care.
In addition, awardees will work with
approximately 30 youth-serving
organizations (YSO) to provide staff
training and develop systematic
approaches to identifying youth who are
at risk for a teen pregnancy and referring
those youth to reproductive health care
services. Finally, awardees will develop
communication campaigns that increase
awareness of the partner health centers’
services for teens. Activities are
expected to result in changes to health
center and YSO partners’ policies, to
staff practices, and to youth health care
seeking and teen pregnancy prevention
behaviors.
Although similar activities have been
implemented in a variety of teen
pregnancy prevention projects, the
proposed combination of efforts, and the
incorporation of youth-friendly best
practices, have not been previously
implemented or evaluated. CDC
therefore plans to collect information
needed to assess these efforts.
Information will be collected from the
CDC awardees, the health center and
YSO partner organizations, and the
youth served by the health center
partner organizations. CDC will use the
information to determine the types of
training and technical assistance that
are needed, to monitor whether
awardees meet objectives related to
health center and YSO partners’ policies
and staff practices, to support a datadriven quality improvement process for
adolescent sexual and reproductive
health care services and referrals, and to
assess whether the project model was
effective in increasing the utilization of
services by youth.
OMB approval is requested for three
years. Participation in the organizational

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Federal Register / Vol. 81, No. 24 / Friday, February 5, 2016 / Notices

assessment activities is required for
awardees and partner organizations.
Participation in the Health Center Youth

Survey is voluntary for youth and will
not involve the collection of identifiable

personal information. There are no costs
to respondents other than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Respondents

Form name

Awardee ..................................................

YSO Staff ................................................

Training and Technical Assistance Tool
Quarterly Performance Measure Reporting Tool.
Annual Performance Measure Reporting
Tool.
Quarterly Performance Measure Reporting Tool.
Annual Performance Measure Reporting
Tool.
Health Center Organizational Assessment.
Health Center Provider Survey ..............
Health Center Youth Survey ..................
Quarterly Performance Measure Reporting Tool.
Annual Performance Measure Reporting
Tool.
Youth Serving Organization (YSO) Organizational Assessment.
YSO Staff Survey ...................................

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

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

Health Center Project Coordinator ..........

Health Center Providers ..........................
Youth .......................................................
YSO Project Coordinator ........................

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. 2016–02173 Filed 2–4–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–0980; Docket No. CDC–2016–
0018]

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

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SUMMARY:

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Jkt 238001

Number of
responses per
respondent

3
3

12
3

2
2

72
18

3

1

6

18

35

3

2

210

35

1

4

140

35

1

2

70

175
1,750
30

1
1
3

30/60
15/60
1

88
438
90

30

1

75/60

38

30

1

1

30

450

1

30/60

225

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

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

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

1,437

Act of 1995. This notice invites
comment on the proposed revision of
the information collection project
entitled National Environmental
Assessment Reporting System (NEARS),
formerly known as the National
Voluntary Environmental Assessment
Information System (NVEAIS). The
NEARS collects data on foodborne
illness outbreaks and environmental
assessments routinely conducted by
food safety programs during outbreak
investigations.
Written comments must be
received on or before April 5, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0018 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.
DATES:

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Average
burden per
response
(in hrs.)

Number of
respondents

Total
burden
(in hrs.)

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
publishing this notice of a proposed
data collection as described below.
Comments are invited on: (a) Whether
the proposed collection of information
FOR FURTHER INFORMATION CONTACT:

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