Agency Information Collection Activities: Proposed Collection; Comment Request, 36590-36591 [2020-12993]
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Federal Register / Vol. 85, No. 117 / Wednesday, June 17, 2020 / Notices
compensation were handled in
compliance with the Commission’s
rules and are not the result of
impermissible financial incentives to
generate calls, and (2) cost and demand
data submitted to the Fund
administrator related to the
determination of compensation rates are
true and correct.
(2) VRS providers shall: (a) Submit to
the Commission and the TRS Fund
administrator a call center report twice
a year and (b) notify the Commission
and the TRS Fund administrator at least
30 days prior to any change to their call
centers’ locations.
(3) VRS providers shall submit
detailed call data records (CDRs) and
speed of answer compliance data to the
Fund administrator.
(4) TRS providers shall use an
automated record keeping system to
capture the CDRs and shall submit such
data electronically in standardized form
to the TRS Fund administrator.
(5) internet-based TRS providers shall
retain the CDRs that are used to support
payment claims submitted to the Fund
administrator for a minimum of five
years, in an electronic format.
(6) VRS providers shall: (a) Maintain
copies of all third-party contracts or
agreements and make them available to
the Commission and the TRS Fund
administrator upon request; and (b)
describe all agreements in connection
with marketing and outreach activities
in their annual submissions to the TRS
Fund administrator.
(7) TRS providers shall provide
information about their TRS
whistleblower protections to all
employees and contractors, in writing.
In 2018, the Commission released the
IP CTS Modernization Order, published
at 83 FR 30082, June 27, 2018, in which
the Commission:
(1) Determined that it would
transition the methodology for IP CTS
cost recovery from the MARS plan to
cost-based rates and adopted interim
rates; and
(2) added two cost reporting
requirements for IP CTS providers: (i) In
annual cost data filings and
supplementary information provided to
the TRS Fund administrator, IP CTS
providers that contract for the supply of
services used in the provision of TRS,
shall include information about
payments under such contracts,
classified according to the substantive
cost categories specified by the TRS
Fund administrator; and (ii) in the
course of an audit or otherwise upon
demand, IP CTS providers must make
available any relevant documentation.
47 CFR 64.604(c)(5)(iii)(D)(1), (6).
VerDate Sep<11>2014
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Federal Communications Commission.
Marlene Dortch,
Secretary.
[FR Doc. 2020–13061 Filed 6–16–20; 8:45 am]
BILLING CODE 6712–01–P
FEDERAL MARITIME COMMISSION
Notice of Agreements Filed
The Commission hereby gives notice
of the filing of the following agreements
under the Shipping Act of 1984.
Interested parties may submit
comments, relevant information, or
documents regarding the agreements to
the Secretary by email at Secretary@
fmc.gov, or by mail, Federal Maritime
Commission, Washington, DC 20573.
Comments will be most helpful to the
Commission if received within 12 days
of the date this notice appears in the
Federal Register. Copies of agreements
are available through the Commission’s
website (www.fmc.gov) or by contacting
the Office of Agreements at (202)–523–
5793 or tradeanalysis@fmc.gov.
Agreement No.: 201305–001.
Agreement Name: CMA CGM/Marfret
Mediterranean—Caribbean/U.S. Gulf
Vessel Sharing Agreement.
Parties: CMA CGM S.A. and
Campagnie Maritime Marfret.
Filing Party: Draughn Arbona; CMA
CGM (America) LLC.
Synopsis: The amendment adds
Jamaica to the geographic scope of the
Agreement.
Proposed Effective Date: 7/20/2020.
Location: https://www2.fmc.gov/
FMC.Agreements.Web/Public/
AgreementHistory/22400.
Dated: June 12, 2020.
Rachel E. Dickon,
Secretary.
Board, if any, are available for
immediate inspection at the Federal
Reserve Bank(s) indicated below and at
the offices of the Board of Governors.
This information may also be obtained
on an expedited basis, upon request, by
contacting the appropriate Federal
Reserve Bank and from the Board’s
Freedom of Information Office at
https://www.federalreserve.gov/foia/
request.htm. Interested persons may
express their views in writing on the
standards enumerated in paragraph 7 of
the Act.
Comments regarding each of these
applications must be received at the
Reserve Bank indicated or the offices of
the Board of Governors, Ann E.
Misback, Secretary of the Board, 20th
Street and Constitution Avenue NW,
Washington, DC 20551–0001, not later
than July 2, 2020.
A. Federal Reserve Bank of St. Louis
(David L. Hubbard, Senior Manager)
P.O. Box 442, St. Louis, Missouri
63166–2034. Comments can also be sent
electronically to
Comments.applications@stls.frb.org:
1. ACE Investments, LLC, Newburg,
Missouri; Aaron C. Espinoza,
individually and as owner of Ace
Investments LLC, also of Newburg,
Missouri; Kyle Espinoza, Nashville,
Tennessee; the Charles G. Bollinger
Revocable Trust, the Velma Bollinger
Marital Trust, Charles G. Bollinger, as
trustee of both trusts, all of Hernando,
Florida; and Faith Limited Partnership,
Charles G. Bollinger, as general partner;
as a group acting in concert to acquire
voting shares of Newburg Insurance
Agency, Inc., and thereby indirectly
acquire voting shares of Citizens Bank of
Newburg, both of Rolla, Missouri.
[FR Doc. 2020–13044 Filed 6–16–20; 8:45 am]
Board of Governors of the Federal Reserve
System, June 12, 2020.
Yao-Chin Chao,
Assistant Secretary of the Board.
BILLING CODE 6730–02–P
[FR Doc. 2020–13052 Filed 6–16–20; 8:45 am]
BILLING CODE P
FEDERAL RESERVE SYSTEM
Change in Bank Control Notices;
Acquisitions of Shares of a Bank or
Bank Holding Company
The notificants listed below have
applied under the Change in Bank
Control Act (Act) (12 U.S.C. 1817(j)) and
§ 225.41 of the Board’s Regulation Y (12
CFR 225.41) to acquire shares of a bank
or bank holding company. The factors
that are considered in acting on the
applications are set forth in paragraph 7
of the Act (12 U.S.C. 1817(j)(7)).
The public portions of the
applications listed below, as well as
other related filings required by the
PO 00000
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10525]
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
SUMMARY:
E:\FR\FM\17JNN1.SGM
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khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 85, No. 117 / Wednesday, June 17, 2020 / Notices
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
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
August 17, 2020.
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
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’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
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:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
16:44 Jun 16, 2020
Jkt 250001
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–10525 PACE Quality Data
Monitoring and Reporting
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: Reinstatement with change of a
previously approved collection; Title:
PACE Quality Data Monitoring and
Reporting; Use: The Programs of AllInclusive Care for the Elderly (PACE)
program is a unique model of managed
care service delivery for the frail elderly,
most of whom are dually-eligible for
Medicare and Medicaid benefits. To be
eligible to enroll in PACE, an individual
must: Be 55 or older, live in the service
area of a PACE organization (PO), need
a nursing home-level of care (as certified
by the state in which he or she lives),
and be able to live safely in the
community with assistance from PACE.
PACE organizations are responsible
for providing all required Medicare and
Medicaid covered services, and any
other service that the interdisciplinary
team (IDT) determines necessary to
improve and maintain a participant’s
overall health condition (42 CFR
460.92). POs must also comply with the
quality monitoring and reporting
requirements outlined in §§ 460.140,
460.200(b)(1), 460.200(c) and 460.202.
POs are also required to report certain
unusual incidents to other Federal and
State agencies consistent with
applicable statutory or regulatory
requirements (see 42 CFR 460.136(a)(5)).
PO 00000
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36591
Form Number: CMS–10525 (OMB
control number: 0938–1264); Frequency:
Annual; Affected Public: Private Sector:
Business or other for-profits; Number of
Respondents: 131; Total Annual
Responses: 1,143; Total Annual Hours:
156,414. (For policy questions regarding
this collection contact Donna
Williamson at 410–786–4647.)
Dated: June 11, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–12993 Filed 6–16–20; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2014–N–0345]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Data To Support
Drug Product Communications as
Used by the Food and Drug
Administration
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA or Agency) is
announcing an opportunity for public
comment on the proposed collection of
certain information by the Agency.
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 of an
existing collection of information, and
to allow 60 days for public comment in
response to the notice. This notice
solicits comments on a generic
clearance to collect information to
support communications used by FDA
about drug products.
DATES: Submit either electronic or
written comments on the collection of
information by August 17, 2020.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before August 17,
2020. The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of August 17, 2020.
Comments received by mail/hand
delivery/courier (for written/paper
submissions) will be considered timely
SUMMARY:
E:\FR\FM\17JNN1.SGM
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Agencies
[Federal Register Volume 85, Number 117 (Wednesday, June 17, 2020)]
[Notices]
[Pages 36590-36591]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2020-12993]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-10525]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing
[[Page 36591]]
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 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 August 17, 2020.
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 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' website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
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: William N. Parham at (410) 786-4669.
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-10525 PACE Quality Data Monitoring and Reporting
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: Reinstatement with
change of a previously approved collection; Title: PACE Quality Data
Monitoring and Reporting; Use: The Programs of All-Inclusive Care for
the Elderly (PACE) program is a unique model of managed care service
delivery for the frail elderly, most of whom are dually-eligible for
Medicare and Medicaid benefits. To be eligible to enroll in PACE, an
individual must: Be 55 or older, live in the service area of a PACE
organization (PO), need a nursing home-level of care (as certified by
the state in which he or she lives), and be able to live safely in the
community with assistance from PACE.
PACE organizations are responsible for providing all required
Medicare and Medicaid covered services, and any other service that the
interdisciplinary team (IDT) determines necessary to improve and
maintain a participant's overall health condition (42 CFR 460.92). POs
must also comply with the quality monitoring and reporting requirements
outlined in Sec. Sec. 460.140, 460.200(b)(1), 460.200(c) and 460.202.
POs are also required to report certain unusual incidents to other
Federal and State agencies consistent with applicable statutory or
regulatory requirements (see 42 CFR 460.136(a)(5)). Form Number: CMS-
10525 (OMB control number: 0938-1264); Frequency: Annual; Affected
Public: Private Sector: Business or other for-profits; Number of
Respondents: 131; Total Annual Responses: 1,143; Total Annual Hours:
156,414. (For policy questions regarding this collection contact Donna
Williamson at 410-786-4647.)
Dated: June 11, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2020-12993 Filed 6-16-20; 8:45 am]
BILLING CODE 4120-01-P