60 day FRN

Federal Register / Vol. 81, No. 232 / Friday, December 2, 2016 / Notices
Ends: 01/03/2017, Contact: Robert
Johnson 305–244–4235.
The U.S. Department of the Interior’s
National Park Service (NPS) is adopting
the U.S. Army Corps of Engineers Final
EIS #20140215, filed with EPA 07/31/
2014. The NPS was not a cooperating
agency for this project. Therefore,
recirculation of the document is
necessary under Section 1506.3(b) of
Council on Environmental Quality
Regulations.
EIS No. 20160284, Draft, TVA, TN,
Multiple Reservoir Land Management
Plans, Comment Period Ends: 01/31/
2017, Contact: Matthew Higdon 865–
632–8051.
Dated: November 29, 2016.
Dawn Roberts,
Management Analyst, NEPA Compliance
Division, Office of Federal Activities.
[FR Doc. 2016–29010 Filed 12–1–16; 8:45 am]
BILLING CODE 6560–50–P

GENERAL SERVICES
ADMINISTRATION
[Notice–WWICC–2016–05; Docket No. 2016–
0006; Sequence No. 5]

World War One Centennial
Commission; Notification of Upcoming
Public Advisory Meeting
World War One Centennial
Commission, GSA.
ACTION: Meeting notice.

asabaliauskas on DSK3SPTVN1PROD with NOTICES

AGENCY:

SUMMARY: Notice of this meeting is being
provided according to the requirements
of the Federal Advisory Committee Act,
5 U.S.C. App. 10(a)(2). This notice
provides the schedule and agenda for
the December 15, 2016 meeting of the
World War One Centennial Commission
(the Commission). The meeting is open
to the public.
DATES: Meeting date: The meeting will
be held on Thursday, December 15,
2016 starting at 9:00 a.m. Eastern
Standard Time (EST), and ending no
later than 10:00 a.m., EST.
The meeting will be held at the
Offices of the World War 1 Centennial
Commission at 1800 G Street NW.,
Washington, DC 20006, Street Level.
This location is handicapped accessible.
The meeting will be open to the public.
Persons attending in person are
requested to refrain from using perfume,
cologne, and other fragrances (see
http://www.access-board.gov/about/
policies/fragrance.htm for more
information).
Written Comments may be submitted
to the Commission and will be made
part of the permanent record of the

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Commission. Comments must be
received by 5:00 p.m., EST, December 9,
2016 and may be provided by email to
daniel.dayton@
worldwar1centennial.gov. Contact
Daniel S. Dayton at daniel.dayton@
worldwar1centennial.org to register to
comment during the meeting’s 30minute public comment period.
Registered speakers/organizations will
be allowed 5 minutes and will need to
provide written copies of their
presentations. Requests to comment,
together with presentations for the
meeting must be received by 5:00 p.m.,
EST, Friday, December 9, 2016. Please
contact Mr. Dayton at the email address
above to obtain meeting materials.
FOR FURTHER INFORMATION CONTACT:
Daniel S. Dayton, Designated Federal
Officer, World War 1 Centennial
Commission, 701 Pennsylvania Avenue
NW., 123, Washington, DC 20004–2608;
or telephone 202–380–0725 (note: this is
not a toll-free number).
SUPPLEMENTARY INFORMATION:
Background
The World War One Centennial
Commission was established by Public
Law 112–272 (as amended), as a
commission to ensure a suitable
observance of the centennial of World
War I, to provide for the designation of
memorials to the service of members of
the United States Armed Forces in
World War I, and for other purposes.
Under this authority, the Committee
will plan, develop, and execute
programs, projects, and activities to
commemorate the centennial of World
War I, encourage private organizations
and State and local governments to
organize and participate in activities
commemorating the centennial of World
War I, facilitate and coordinate activities
throughout the United States relating to
the centennial of World War I, serve as
a clearinghouse for the collection and
dissemination of information about
events and plans for the centennial of
World War I, and develop
recommendations for Congress and the
President for commemorating the
centennial of World War I. The
Commission does not have an
appropriation and operated solely on
donated funds.
Agenda: Thursday, December 15, 2016
Old Business
• Acceptance of minutes of last
meeting.
• Public Comment Period.
New Business
• Executive Director’s Report—Mr.
Dayton.

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• Fundraising Report—Ambassador
Sedgwick.
• Memorial Report—Mr. Fountain.
• Education Report—Dr. O’Connell.
• Endorsements—(RFS)—Dr.
Seefried.
• International Report—Dr. Seefried.
• Report on April 6 Event—Dr.
Seefried.
Other Business
• Chairman’s Report.
• Set Next Meeting.
• Motion to Adjourn.
Dated: November 28, 2016.
Daniel S. Dayton,
Designated Federal Official, World War I
Centennial Commission.
[FR Doc. 2016–28920 Filed 12–1–16; 8:45 am]
BILLING CODE 6820–95–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17FB; Docket No. CDC–2016–
0113]

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 proposed information
collection entitled ‘‘Understanding
Relationship Dynamics and Conflict
Survey.’’ CDC will use the information
collected to ascertain which factors or
groups of factors may influence violence
perpetration that occurs within adult
intimate partner relationships.
DATES: Written comments must be
received on or before January 31, 2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0113 by any of the following methods:
• Federal eRulemaking Portal:
Regulations.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,

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87038

Federal Register / Vol. 81, No. 232 / Friday, December 2, 2016 / Notices

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: [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
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.

across various IPV research domains
(e.g., etiology, prevention efficacy and
intervention effectiveness) tend to view
IPV as an isolated occurrence and rarely
consider the contextual situation in
which IPV occurs. For example, existing
models may not distinguish between an
act of physical violence perpetrated
during an argument from an act of
physical violence perpetrated as a
constellation of physical, sexual, and
psychological violence by one partner
toward another for the purpose of
dominating and controlling that partner.
To that end, we need more
information about the factors or groups
of factors that influence violence
perpetration within adult intimate
partner relationships. This project will
take a critical first step by collecting
information from adults in the United
States about their attitudes, perceptions,
beliefs and experiences with violence in
intimate relationships. In the future, this
information can help develop a
standardized measurement scheme that
will distinguish among different
contextual forms of IPV perpetration so
that effective violence prevention
strategies can be targeted and
implemented.
The respondent universe consists of
2,210 adults (18 years or older) from two
populations: The general population
who live in the United States and
incarcerated individuals who live in
Indiana. Half of the incarcerated group
will have an IPV-related offense record
and half will not. Data will be collected
through an online survey of Mechanical
Turk (MT) workers and an in-person
survey of incarcerated individuals. Data
analysis will include a combination of
Factor Analysis and Latent Profile
Analysis.
CDC will seek a two-year approval
from the Office of for this new
collection. There are no cost to
respondents other than their time spent
responding to the survey/screener.

Proposed Project
Understanding Relationship
Dynamics and Conflict Survey—New—
National Center for Injury Prevention
and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Intimate partner violence (IPV) is a
substantial public health problem in the
United States. Over a third of women
and over a quarter of men have
experienced rape, physical violence,
and/or stalking by an intimate partner.
Recognition of the importance and
prevalence of this issue has fueled
research to examine the causes,
correlates, and outcomes of IPV over the
past several decades. However, studies

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ESTIMATED ANNUALIZED BURDEN HOURS
Response
burden
(hours)

Form name

Mechanical Turk Survey Respondents.
Mechanical Turk Survey Respondents.

Screener ...........................................

4,300

1

5/60

358

Understanding Relationship Dynamics and.
Conflict .............................................
Understanding Relationship Dynamics and Conflict.

1,000

1

1

1,000

105

1

75/60

131

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

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

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

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

1,489

Incarcerated Survey Respondents ...
Total ...........................................

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Number of
respondents

Number of
responses per
respondent

Type of
respondents

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Total burden
hours

Federal Register / Vol. 81, No. 232 / Friday, December 2, 2016 / Notices
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. 2016–28899 Filed 12–1–16; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–26]

Agency Information Collection
Activities: Proposed Collection;
Comment Request

asabaliauskas on DSK3SPTVN1PROD with NOTICES

AGENCY: Centers for Medicare &
Medicaid Services.
ACTION: Notice.
SUMMARY: 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
any of the following subjects: The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
the accuracy of the estimated burden;
ways to enhance the quality, utility, and
clarity of the information to be
collected; and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
January 31, 2017.
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 http://
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.

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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 ____, 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
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
http://www.cms.hhs.gov/Paperwork
ReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
[email protected].
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–R–26 Clinical Laboratory
Improvement Amendments (CLIA)
Regulations
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
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Clinical

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Laboratory Improvement Amendments
(CLIA) Regulations; Use: The
information is necessary to determine
an entity’s compliance with the
Congressionally-mandated program
with respect to the regulation of
laboratory testing (CLIA). In addition,
laboratories participating in the
Medicare program must comply with
CLIA requirements as required by
section 6141 of OBRA 89. Medicaid,
under the authority of section
1902(a)(9)(C) of the Social Security Act,
pays for services furnished only by
laboratories that meet Medicare (CLIA)
requirements. Form Number: CMS–R–
26 (OMB Control Number: 0938–0612);
Frequency: Monthly, occasionally;
Affected Public: Private sector—
Business or other for-profits and Notfor-profit institutions, State, Local or
Tribal Governments, and the Federal
government; Number of Respondents:
70,861; Total Annual Responses:
1,979,300; Total Annual Hours:
14,975,785. (For policy questions
regarding this collection contact Raelene
Perfetto at 410–786–6876).
Dated: November 29, 2016.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2016–29011 Filed 12–1–16; 8:45 am]
BILLING CODE 4120–01– P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10340, CMS–
10476, CMS–10525, and CMS–10630]

Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
SUMMARY: 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
(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
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any

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