Agency Forms Undergoing Paperwork Reduction Act Review, 29266-29268 [2016-11036]
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29266
Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices
Agreement No.: 012408.
Title: WWL/Grimaldi Euromed SPA
Space Charter Agreement.
Parties: Wallenius Wilhelmsen
Logistics AS and Grimaldi Euromed
SPA.
Filing Party: Wayne R. Rohde, Esq.;
Cozen O’Connor LLP; 1200 Nineteenth
St. NW.; Washington, DC 200036.
Synopsis: The Agreement authorizes
the parties to charter space to/from one
another on an ‘‘as needed/as available’’
basis in the trade between ports on the
Atlantic Coast of the United States and
ports in North Europe and on the
Mediterranean Sea.
Agreement No.: 012409.
Title: CMA CGM/COSCON Slot
Exchange Agreement Asia—U.S. West
Coast.
Parties: CMA CGM S.A. and COSCO
Container Lines Company, Limited.
Filing Party: Eric. C. Jeffrey, Esq.;
Nixon Peabody LLP; 799 9th Street NW.,
Suite 500; Washington, DC 20001.
Synopsis: The agreement authorizes
the parties to exchange slots on their
respective services in the trade between
the United States West Coast and the
People’s Republic of China (including
Hong Kong), Singapore, Malaysia,
Vietnam, and Canada.
Agreement No.: 201202–009.
Title: Oakland MTO Agreement.
Parties: Everport Terminal Services,
Inc.; SSA Terminals, LLC; SSA
Terminals (Oakland), LLC; and Trapac,
Inc.
Filing Party: Wayne R. Rohde, Esq.;
Cozen O’Connor; 1200 19th Street NW.;
Washington, DC 20036.
Synopsis: The amendment deletes
Ports America Outer Harbor Terminal,
LLC as a party to the Agreement.
By Order of the Federal Maritime
Commission.
Dated: May 6, 2016.
Rachel E. Dickon,
Assistant Secretary.
[FR Doc. 2016–11084 Filed 5–10–16; 8:45 am]
BILLING CODE 6731–AA–P
FEDERAL MARITIME COMMISSION
[DOCKET NO. 16–11]
mstockstill on DSK3G9T082PROD with NOTICES
Notice of Filing of Complaint and
Assignment—Correction
LANDERS BROTHERS AUTO GROUP, INC.
D/B/A LANDERS HONDA (JONESBORO),
LANDERS BROTHERS AUTO NO. 4, LLC
D/B/A/LANDERS HONDA (PINE BLUFF),
INDIVIDUALLY AND ON BEHALF OF
OTHERS SIMILARLY SITUATED
V.
NIPPON YUSEN KABUSHIKI KAISHA, NYK
LINE (NORTH AMERICA) INC., MITSUI
O.S.K. LINES, LTD., MITSUI O.S.K. BULK
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SHIPPING (USA), INC., WORLD
¨
LOGISTICS SERVICE (USA) INC., HOEGH
¨
AUTOLINERS AS, HOEGH AUTOLINERS,
INC., NISSAN MOTOR CAR CARRIERS
CO. LTD., KAWASAKI KISEN KAISHA,
LTD., ‘‘K’’ LINE AMERICA, INC.,
WALLENIUS WILHELMSEN LOGISTICS
AS, WALLENIUS WILHELMSEN
LOGISTICS AMERICAS LLC, EUKOR CAR
˜´
CARRIERS INC., COMPANIA SUD
AMERICANA DE VAPORES S.A., AND
CSAV AGENCY NORTH AMERICA, LLC
In a Notice of Filing of Complaint and
Assignment published on Wednesday,
May 4, 2016, 81 FR 26793, the last
sentence stated that ‘‘[t]he initial
decision of the presiding officer in this
proceeding shall be issued by April 28,
2017 and the final decision of the
Commission shall be issued by
November 13, 2017.’’ Due to a clerical
error, the date for the initial decision
was incorrect. That sentence is
corrected to read as follows: ‘‘The initial
decision of the presiding officer in this
proceeding shall be issued by May 12,
2017 and the final decision of the
Commission shall be issued by
November 13, 2017.’’
Karen V. Gregory,
Secretary.
[FR Doc. 2016–11019 Filed 5–10–16; 8:45 am]
BILLING CODE 6731–AA–P
FEDERAL MINE SAFETY AND HEALTH
REVIEW COMMISSION
[BAC 6735–01]
Sunshine Act Notice
May 9, 2016.
10:00 a.m., Thursday,
May 19, 2016.
PLACE: The Richard V. Backley Hearing
Room, Room 511N, 1331 Pennsylvania
Avenue NW., Washington, DC 20004
(enter from F Street entrance).
STATUS: Open.
MATTERS TO BE CONSIDERED: The
Commission will consider and act upon
the following in open session: Secretary
of Labor v. KenAmerican Resources,
Inc., Docket No. KENT 2013–0211.
(Issues include whether the Judge erred
in vacating an alleged violation of a
standard which prohibits advanced
notice of an inspection.)
Any person attending this meeting
who requires special accessibility
features and/or auxiliary aids, such as
sign language interpreters, must inform
the Commission in advance of those
needs. Subject to 29 CFR 2706.150(a)(3)
and § 2706.160(d).
CONTACT PERSON FOR MORE INFO:
Emogene Johnson (202) 434–9935/(202)
TIME AND DATE:
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708–9300 for TDD Relay/1–800–877–
8339 for toll free.
Sarah L. Stewart,
Deputy General Counsel.
[FR Doc. 2016–11202 Filed 5–9–16; 4:15 pm]
BILLING CODE P
FEDERAL MINE SAFETY AND HEALTH
REVIEW COMMISSION
[BAC 6735–01]
Sunshine Act Notice
May 9, 2016.
10:00 a.m., Wednesday,
May 18, 2016.
PLACE: The Richard V. Backley Hearing
Room, Room 511N, 1331 Pennsylvania
Avenue NW., Washington, DC 20004
(enter from F Street entrance).
STATUS: Closed.
MATTERS TO BE CONSIDERED: The
Commission will consider and act upon
the following in closed session as a
continuation of the meeting held on
May 4, 2016: Secretary of Labor v.
Newtown Energy, Inc., Docket No.
WEVA 2011–283 (Issues include
whether the Administrative Law Judge
erred by concluding that the violation in
question was not significant and
substantial and was not the result of an
unwarrantable failure to comply.)
Any person attending this meeting
who requires special accessibility
features and/or auxiliary aids, such as
sign language interpreters, must inform
the Commission in advance of those
needs. Subject to 29 CFR 2706.150(a)(3)
and § 2706.160(d).
CONTACT PERSON FOR MORE INFO:
Emogene Johnson (202) 434–9935/(202)
708–9300 for TDD Relay/1–800–877–
8339 for toll free.
TIME AND DATE:
Sarah Stewart,
Deputy General Counsel.
[FR Doc. 2016–11199 Filed 5–9–16; 4:15 pm]
BILLING CODE 6735–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–16–0822]
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
E:\FR\FM\11MYN1.SGM
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29267
Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 2016 / Notices
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
by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
Proposed Project
The National Intimate Partner and
Sexual Violence Survey (NISVS) (OMB
Control No. 0920–0822, expiration date
6/30/2016)—Revision — National
Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
This is a revision request for the
currently approved National Intimate
Partner and Sexual Violence Survey
(NISVS). OMB approval is requested for
three years.
In 2010, NISVS reported that
approximately 6.9 million women and
5.6 million men experienced rape,
physical violence and/or stalking by an
intimate partner within the last year.
The health care costs of Intimate Partner
Violence (IPV) exceed $5.8 billion each
year, nearly $3.9 billion of which is for
direct medical and mental health care
services.
In order to address this important
public health problem, CDC
implemented, beginning in 2010, the
National Intimate Partner and Sexual
Violence Surveillance System that
produces national and state level
estimates of IPV, Sexual Violence (SV)
and stalking on an annual basis. CDC is
requesting a continuation of data
collection among non-institutionalized
adult men and women aged 18 years or
older in the United States assessing
lifetime experiences of IPV, SV and
stalking with a new and improved data
collection tool. The revisions to the
survey are aimed at reducing the time
and complexity of the instrument, thus
reducing the burden on the respondent.
The simplified structure of the
instrument will also reduce the
complexity of the data set, making it
more assessable for public use.
Additionally, in collaboration with the
Department of Defense (DoD), NISVS
will collect information regarding the
experiences of IPV, SV and stalking
among active duty women and men in
the military and wives of active duty
men.
Data collected are used by local, state
and national governments and
organizations to inform prevention
programs and policy making related to
intimate partner violence, sexual
violence and stalking. This data
collection will take place during the
first three months of data collection.
Data are analyzed using appropriate
statistical software to account for the
complexity of the survey design to
compute weighted counts, percentages,
confidence intervals using both national
and state level data.
To comply with OMB requirements,
CDC is developing an expert panel to
address methodological issues with the
NISVS survey. The panel will meet
multiple times over the course of the
next year. The members of this panel
will provide guidance on how to
improve both survey design (methods,
sampling frame, recruitment, mode of
administration) and content/question
wording with the goals of increasing
response rates, reducing non-response
bias, and maximizing the opportunities
across Federal surveys for covering
populations of interest. The survey will
be conducted among English or Spanish
speaking male and female adults (18
years and older) living in the United
States. The estimated annual burden
hours are 27,106. There are no extra
costs to respondents.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Form name
Non-Participating Household (Screened) .......
NISVS Survey Instrument. First section nonparticipating.
NISVS Survey Instrument. Section for participating.
NISVS Survey Instrument. Section for DoD
participating.
NISVS Survey Instrument. Section for participating.
Eligible Household (Completes Survey) .........
Non-Participating DoD Household (Screened)
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Eligible DoD Household (Completes Survey)
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Number of
responses per
respondent
Average
burden per
response
(in hours)
170,000
1
3/60
25,000
1
25/60
73,800
1
3/60
10,800
1
25/60
E:\FR\FM\11MYN1.SGM
11MYN1
29268
Federal Register / Vol. 81, No. 91 / Wednesday, May 11, 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. 2016–11036 Filed 5–10–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10261, CMS–
10295 and CMS–10463]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
ACTION: Notice.
AGENCY:
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 require; 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: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
DATES: Comments must be received by
July 11, 2016.
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 https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
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SUMMARY:
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Jkt 238001
document(s) that are accepting
comments.
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
https://www.cms.hhs.gov/
PaperworkReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
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–10261 Part C Medicare
Advantage Reporting Requirements and
Supporting Regulations in 42 CFR
422.516(a)
CMS–10295 Reporting Requirements
for States Under Transitional Medical
Assistance (TMA) Provisions
CMS–10463 Cooperative Agreement
To Support Navigators in FederallyFacilitated and State Partnership
Exchanges
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
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collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Part C Medicare
Advantage Reporting Requirements and
Supporting Regulations in 42 CFR
422.516(a); Use: Medicare Advantage
Organizations (MAOs) must have an
effective procedure to develop, compile,
evaluate, and report to CMS, to its
enrollees, and to the general public, at
the times and in the manner that CMS
requires, and while safeguarding the
confidentiality of the doctor-patient
relationship, statistics and other
information with respect to: the cost of
its operations; the patterns of service
utilization; the availability,
accessibility, and acceptability of its
services; to the extent practical,
developments in the health status of its
enrollees; information demonstrating
that the MAO has a fiscally sound
operation; and other matters that CMS
may require. CMS also has oversight
authority over cost plans which
includes establishment of reporting
requirements. This revision would add
five new data elements to the reporting
section: Organization Determinations
and Reconsiderations. These new data
elements are needed to obtain more
information about case reopenings. The
revision would also suspend the
Sponsor Oversight of Agents reporting
section beginning 2017 so that the
reporting section can be reassessed
based on burden and usage. Form
Number: CMS–10261 (OMB control
number: 0938–1054); Frequency: Yearly
and Semi-annually; Affected Public:
Private sector (Business or other Forprofits); Number of Respondents: 544;
Total Annual Responses: 3,508; Total
Annual Hours: 160,215. (For policy
questions regarding this collection
contact Terry Lied at 410–786–8973).
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Reporting
Requirements for States Under
Transitional Medical Assistance (TMA)
Provisions; Use: The HHS Secretary is
required to submit annual reports to
Congress with information collected
from states in accordance with section
5004(d) of the American Recovery and
Reinvestment Act of 2009. Medicaid
agencies in 50 states complete the
reports while we review the information
to determine if each state has met all of
the reporting requirements specified
under section 5004(d). Form Number:
E:\FR\FM\11MYN1.SGM
11MYN1
Agencies
[Federal Register Volume 81, Number 91 (Wednesday, May 11, 2016)]
[Notices]
[Pages 29266-29268]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-11036]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-16-0822]
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
[[Page 29267]]
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 by fax to (202) 395-5806. Written
comments should be received within 30 days of this notice.
Proposed Project
The National Intimate Partner and Sexual Violence Survey (NISVS)
(OMB Control No. 0920-0822, expiration date 6/30/2016)--Revision --
National Center for Injury Prevention and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
This is a revision request for the currently approved National
Intimate Partner and Sexual Violence Survey (NISVS). OMB approval is
requested for three years.
In 2010, NISVS reported that approximately 6.9 million women and
5.6 million men experienced rape, physical violence and/or stalking by
an intimate partner within the last year. The health care costs of
Intimate Partner Violence (IPV) exceed $5.8 billion each year, nearly
$3.9 billion of which is for direct medical and mental health care
services.
In order to address this important public health problem, CDC
implemented, beginning in 2010, the National Intimate Partner and
Sexual Violence Surveillance System that produces national and state
level estimates of IPV, Sexual Violence (SV) and stalking on an annual
basis. CDC is requesting a continuation of data collection among non-
institutionalized adult men and women aged 18 years or older in the
United States assessing lifetime experiences of IPV, SV and stalking
with a new and improved data collection tool. The revisions to the
survey are aimed at reducing the time and complexity of the instrument,
thus reducing the burden on the respondent. The simplified structure of
the instrument will also reduce the complexity of the data set, making
it more assessable for public use. Additionally, in collaboration with
the Department of Defense (DoD), NISVS will collect information
regarding the experiences of IPV, SV and stalking among active duty
women and men in the military and wives of active duty men.
Data collected are used by local, state and national governments
and organizations to inform prevention programs and policy making
related to intimate partner violence, sexual violence and stalking.
This data collection will take place during the first three months of
data collection. Data are analyzed using appropriate statistical
software to account for the complexity of the survey design to compute
weighted counts, percentages, confidence intervals using both national
and state level data.
To comply with OMB requirements, CDC is developing an expert panel
to address methodological issues with the NISVS survey. The panel will
meet multiple times over the course of the next year. The members of
this panel will provide guidance on how to improve both survey design
(methods, sampling frame, recruitment, mode of administration) and
content/question wording with the goals of increasing response rates,
reducing non-response bias, and maximizing the opportunities across
Federal surveys for covering populations of interest. The survey will
be conducted among English or Spanish speaking male and female adults
(18 years and older) living in the United States. The estimated annual
burden hours are 27,106. There are no extra costs to respondents.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Non-Participating Household (Screened) NISVS Survey Instrument. 170,000 1 3/60
First section non-
participating.
Eligible Household (Completes Survey). NISVS Survey Instrument. 25,000 1 25/60
Section for
participating.
Non-Participating DoD Household NISVS Survey Instrument. 73,800 1 3/60
(Screened). Section for DoD
participating.
Eligible DoD Household (Completes NISVS Survey Instrument. 10,800 1 25/60
Survey). Section for
participating.
----------------------------------------------------------------------------------------------------------------
[[Page 29268]]
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. 2016-11036 Filed 5-10-16; 8:45 am]
BILLING CODE 4163-18-P