60d FRN - published

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Federal Register / Vol. 82, No. 134 / Friday, July 14, 2017 / Notices
Total Estimated Number of Annual
Burden Hours: 227.
Abstract: As requested by the
shipping public and the regulated
industry, the Commission, through
CADRS, provides ombuds and
mediation services to assist parties in
resolving international ocean cargo
shipping or passenger vessel (cruise)
disputes without resorting to litigation
or administrative adjudication. These
functions focus on addressing issues
that members of the regulated industry
and the shipping public may encounter
at any stage of a commercial or customer
dispute. In order to provide its ombuds
and mediation services, CADRS needs
certain identifying information about
the involved parties, shipments, and
nature of the dispute. In response to
requests for assistance from the public,
CADRS requests this information from
parties seeking its assistance. The
collection and use of this information
on a cargo or cruise dispute is integral
to CADRS staff’s ability to efficiently
review the matter and provide
assistance. Aggregated information may
be used for statistical purposes.
Currently, this information is collected
in a non-uniform manner in response to
requests for CADRS assistance. http://
www.fmc.gov/resources/requesting_
cadrs_assistance.aspx
As required by the Administrative
Dispute Resolution Act (ADRA), 5
U.S.C. 571–574, the information
contained in these forms is treated as
confidential and subject to the same
confidentiality provisions as
administrative dispute resolutions
pursuant to 5 U.S.C. 574. Except as
specifically set forth in 5 U.S.C. 574,
neither CADRS staff nor the parties to a
dispute resolution shall disclose any
informal dispute resolution
communication.
This information collection is subject
to the PRA. The FMC may not conduct
or sponsor a collection of information,
and the public is not required to
respond to an information collection,
unless it is approved by the OMB under
the PRA and displays a currently valid
OMB Control Number. In addition,
notwithstanding any other provisions of
law, no person shall be subject to
penalty for failing to comply with a
collection of information that does not
display a valid Control Number. See 5
CFR 1320.5(a) and 1320.6.

FEDERAL MARITIME COMMISSION

AGENCY HOLDING THE MEETING:

Federal

Maritime Commission.
TIME AND DATE:

July 19, 2017; 10:00 a.m.

800 N. Capitol Street NW., First
Floor Hearing Room, Washington, DC.

PLACE:

The first portion of the meeting
will be held in Open Session; the
second portion will be held in Closed
Session.

STATUS:

MATTERS TO BE CONSIDERED:

1. Controlled Carrier List Update
Closed Session
1. Staff Briefing on the West Coast MTO
Discussion Agreement (FMC No.
201143)
2. Staff Briefing on the Transpacific
Stabilization Agreement (FMC No.
011223)
CONTACT PERSON FOR MORE INFORMATION:

Rachel E. Dickon, Assistant Secretary,
(202) 523–5725.
Rachel E. Dickon
Assistant Secretary.
[FR Doc. 2017–14942 Filed 7–12–17; 4:15 pm]
BILLING CODE 6730–01–P

DEPARTMENT OF DEFENSE
GENERAL SERVICES
ADMINISTRATION
NATIONAL AERONAUTICS AND
SPACE ADMINISTRATION
[OMB Control No. 9000–0089; Docket No.
2017–0053; Sequence 3]

Information Collection; Request for
Authorization of Additional
Classification and Rate, Standard Form
1444
Correction

[FR Doc. 2017–14760 Filed 7–13–17; 8:45 am]

[FR Doc. C1–2017–08670 Filed 7–13–17; 8:45 am]

BILLING CODE 6731–AA–P

BILLING CODE 1301–00–D

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Centers for Disease Control and
Prevention
[60Day–17–0909; Docket No. CDC–2017–
0053]

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 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. This notice invites
comment on the CDC information
collection project titled ‘‘CDC Diabetes
Prevention Recognition Program
(DPRP).’’ This revision of DPRP
Standards and Operating Procedures
(i.e., DPRP Standards)will allow
continued collection of nationwide, deidentified data against the
implementation of the National Diabetes
Prevention Programs (National DPPs)
using a set of evidence-based standards.
CDC uses this data to effectively manage
the DPRP.
DATES: Written comments must be
received on or before September 12,
2017.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2017–
0053 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,
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.
SUMMARY:

Open Session

Rachel Dickon,
Assistant Secretary.

VerDate Sep<11>2014

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

Sunshine Act Meeting

In notice document 2017–08670
appearing on pages 20340–20341 in the
issue of May 1, 2017, make the
following correction:
On page 20341, in the second column,
under the heading B. Annual Reporting
Burden, the fourth line down, ‘‘Review
time per response: 5.’’ should read
‘‘Review time per response: .5.’’.

Authority: 46 U.S.C. 40101 et seq.

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Federal Register / Vol. 82, No. 134 / Friday, July 14, 2017 / Notices

To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Leroy A.
Richardson, 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.

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FOR FURTHER INFORMATION CONTACT:

VerDate Sep<11>2014

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Proposed Project
CDC Diabetes Prevention Recognition
Program (DPRP) (OMB Control Number
0920–0909, exp. 12/31/2017)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC’s Division of Diabetes
Translation (DDT) established and
administers the National DPP’s Diabetes
Prevention Recognition Program
(DPRP), which recognizes organizations
that deliver diabetes prevention
programs according to evidence-based
requirements set forth in the ‘‘Centers
for Disease Control and Prevention
Recognition Program Standards and
Operating Procedures’’ (DPRP
Standards). Additionally, the Centers for
Medicare and Medicaid Services (CMS)
Medicare Diabetes Prevention Program
(MDPP) expansion of CDC’s National
DPP was announced in early 2016,
when the Secretary of Health and
Human Services determined that the
Diabetes Prevention Program met the
statutory criteria for inclusion in
Medicare’s expanded list of healthcare
services for beneficiaries (https://
innovation.cms.gov/initiatives/
medicare-diabetes-preventionprogram/). This is the first time a
preventive service model from the CMS
Innovation (CMMI) Center has been
expanded. After extensive testing of the
DPP model in 17 sites across the U.S. in
2014–2016, CMS proposed the MDPP in
Sections 1102 and 1871 of the Social
Security Act (42 U.S.C. 1302 and
1395hh § 424.59), authorizing CDCrecognized organizations to prepare for
enrollment as MDPP suppliers
beginning in January 2018 in order to
bill CMS for these services Only
organizations in good standing with the
CDC DPRP will be eligible as MDPP
suppliers.
CDC requests an additional three-year
OMB approval to continue collecting
the information needed to administer
the DPRP and information needed by
CMS to support the MDPP benefit.
Based on experience with the DPRP
from 2011–2017, and feedback from
applicant organizations and internal and
external partners, CDC plans to revise
the DPRP Standards and the associated
information collection.
Key changes relate to incorporation of
variables needed to ensure the seamless
implementation of the CMS MDPP
benefit. The majority of the additional
data elements included in the current
Standards revision are the result of new
CMS requirements for MDPP suppliers.

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In particular, CMS is requiring deidentified participant-level data
submission every 6 months. While data
submissions every 6 months are
included to align with the CMS MDPP
supplier requirements, this change will
also benefit organizations that are not
MDPP suppliers, as it will allow them
to receive more feedback in an effort to
make necessary mid-course corrections
and successfully achieve either
preliminary or full recognition status.
Semiannual evaluation of organization
performance was part of the initial 2011
OMB approval for CDC’s DPRP
information collection.
One data element has been revised
and eleven additional data elements
have been added in either the one-time
application form or within the
evaluation data elements:
Application Form
(1) Class Type (revised)
(2) Organization Type (new)
(3) Lifestyle Coach Training Entity
(new)
(4) CDC Grantee (yes/no) (new)
Evaluation Data Elements
(6) Participant’s Education (new)
(7) Delivery Mode (new)
(8) Session ID (new)
(9) Session Type (new)
(10) Lifestyle Coach Medicare National
Provider Identification Number as
Supplied by CMS (new)
(11) Enrollment Source (new)
(12) Payer Type (new)
Additional changes to the DPRP
Standards or DPRP information
collection may be requested during the
period of the Revision request, as CDC
continues discussions with recognized
programs and potential applicants and
reviews results from ongoing studies.
During the period of this Revision,
CDC estimates receipt of approximately
500 DPRP application forms per year.
The estimated burden per one-time, upfront application response is 1 hours
(annualized to 500 hours one-time
across all new organizations). In
addition, CDC estimates receipt of semiannual evaluation data submissions
from the same 500 additional
organizations per year; estimated at 2
hours per response. The total estimated
average annualized evaluation burden to
respondents is 7,676 hours. This
includes an estimate of the time needed
to extract and compile the required data
records and fields from an existing
electronic database, review the data,
create or enter a data file in the required
format (i.e., CSV file), and submit the
data file via the National DPP Web site.
The estimated burden per response is
modest since the information requested

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Federal Register / Vol. 82, No. 134 / Friday, July 14, 2017 / Notices
for DPRP recognition is routinely
collected by most organizations that
deliver lifestyle change programs for
their own internal evaluation and
possible insurance reimbursement

purposes, including Medicare under the
forthcoming MDPP benefit.
Participation in the DPRP is voluntary,
data are de-identified, no Personally
Identifiable Information is collected by

CDC, and there are no costs to
respondents other than their time. CDC
seeks to request a three-year approval.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Avg. burden
per response
(in hours)

Total burden
(in hours)

Form name

Public sector organizations that deliver type 2 diabetes prevention
programs.

DPRP Application Form ..............

150

1

1

150

DPRP Evaluation Data ................
DPRP Application Form ..............

350
350

2
1

2
1

1,400
350

DPRP Evaluation Data ................

1,444

2

2

5,776

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

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

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

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

7,676

Private sector organizations that deliver type 2 diabetes prevention
programs.
Total ............................................

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. 2017–14792 Filed 7–13–17; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–17–17AMO; Docket No. CDC–2017–
0054]

Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).

AGENCY:

ACTION:

Notice with comment period.

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
comments on a proposed information
collection project titled ‘‘Assessment of
Restaurant Ill Worker Policies.’’

SUMMARY:

mstockstill on DSK30JT082PROD with NOTICES

Number of
respondents

Type of respondent

Written comments must be
received on or before September 12,
2017.

DATES:

VerDate Sep<11>2014

17:44 Jul 13, 2017

Jkt 241001

You may submit comments,
identified by Docket No. CDC–2017–
0054 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,
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.

ADDRESSES:

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 Leroy A.
Richardson, 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
FOR FURTHER INFORMATION CONTACT:

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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

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