Agency Information Collection Activities: Submission for OMB Review; Comment Request, 67722-67723 [2018-27337]
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Federal Register / Vol. 83, No. 249 / Monday, December 31, 2018 / Notices
clicking on the links or querying the
docket number.
Any person desiring to intervene or
protest in any of the above proceedings
must file in accordance with Rules 211
and 214 of the Commission’s
Regulations (18 CFR 385.211 and
385.214) on or before 5:00 p.m. Eastern
time on the specified comment date.
Protests may be considered, but
intervention is necessary to become a
party to the proceeding.
eFiling is encouraged. More detailed
information relating to filing
requirements, interventions, protests,
service, and qualifying facilities filings
can be found at: https://www.ferc.gov/
docs-filing/efiling/filing-req.pdf. For
other information, call (866) 208–3676
(toll free). For TTY, call (202) 502–8659.
Dated: December 21, 2018.
Nathaniel J. Davis, Sr.,
Deputy Secretary.
Dated: December 21, 2018.
Rachel Dickon,
Secretary.
[FR Doc. 2018–28407 Filed 12–28–18; 8:45 am]
BILLING CODE 6731–AA–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[FR Doc. 2018–28412 Filed 12–28–18; 8:45 am]
[Document Identifier CMS–R–74]
BILLING CODE 6717–01–P
khammond on DSK30JT082PROD with NOTICES
Kaisha, Ltd. as parties due to the
creation of Ocean Network Express Pte.
Ltd., and redesignates Yang Ming
Marine Transport Corp. as a nonOCEMA ocean common carrier party to
the agreement due to its earlier
withdrawal from OCEMA.
Proposed Effective Date: 12/17/2018.
Location: https://www2.fmc.gov/
FMC.Agreements.Web/Public/
AgreementHistory/454.
FEDERAL MARITIME COMMISSION
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Notice of Agreement Filed
AGENCY:
The Commission hereby gives notice
of the filing of the following agreement
under the Shipping Act of 1984.
Interested parties may submit comments
on the agreement to the Secretary by
email at Secretary@fmc.gov, or by mail,
Federal Maritime Commission,
Washington, DC 20573, within twelve
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.: 011962–015.
Agreement Name: Consolidated
Chassis Management Pool Agreement.
Parties: American President Lines,
Ltd.; APL Co. Pte. Ltd.; CMA CGM S.A.;
COSCO Shipping Lines Co., Ltd.;
Evergreen Line Joint Service Agreement;
Hamburg Sud; Hapag-Lloyd AG; HapagLloyd USA, LLC; Hyundai Merchant
Marine Co., Ltd.; Maersk Line A/S;
Matson Navigation Company, Inc.;
Mediterranean Shipping Company S.A.;
Orient Overseas Container Line Limited;
Westwood Shipping Lines, Inc.; Yang
Ming Marine Transport Corporation;
Zim Integrated Shipping Services Ltd.;
and Ocean Network Express Pte. Ltd.
Filing Party: Donald Kassilke; Cozen
O’Connor.
Synopsis: The amendment deletes
Mitsui O.S.K. Lines, Ltd.; Nippon Yusen
Kaisha Line; and Kawasaki Kisen
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16:24 Dec 28, 2018
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Centers for Medicare &
Medicaid Services, Department of
Health and Human Services.
ACTION: Notice.
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
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.
SUMMARY:
Comments on the collection(s) of
information must be received by the
OMB desk officer by January 30, 2019.
ADDRESSES: When commenting on the
proposed information collections,
DATES:
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please reference the document identifier
or OMB control number. To be assured
consideration, comments and
recommendations must be received by
the OMB desk officer via one of the
following transmissions: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
Number: (202) 395–5806 OR, Email:
OIRA_s submission@omb.eop.gov.
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/
PaperworkReductionActof1995/PRAListing.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 Parham at (410) 786–4669.
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. 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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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 that summarizes
the following proposed collection(s) of
information for public comment:
Information Collection
Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Income and
Eligibility Verification System Reporting
and Supporting Regulations; Use:
Section 1137 of the Social Security Act
requires that States verify the income
and eligibility information contained on
the applicant’s application and in the
applicant’s case file through data
matches with the agencies and entities
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Federal Register / Vol. 83, No. 249 / Monday, December 31, 2018 / Notices
identified in this section. The State
Medicaid/CHIP agency will report the
existence of a system to collect all
information needed to determine and
redetermine eligibility for Medicaid and
CHIP. The State Medicaid/CHIP agency
will attest to using the PARIS system in
determining beneficiary eligibility in
Medicaid or CHIP benefit programs.
Form Number: CMS–R–74 (OMB control
number: 0938–0467); Frequency:
Occasionally; Affected Public: State,
Local, or Tribal Governments; Number
of Respondents: 55; Total Annual
Responses: 3,241; Total Annual Hours:
1,071. (For policy questions regarding
this collection contact Stephanie Bell at
410–786–0617.)
Dated: December 13, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–27337 Filed 12–28–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–3356–NC]
RIN 0938–AT56
Medicare Program; Clinical Laboratory
Improvement Amendments of 1988
(CLIA) Fees
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Notice with comment period.
AGENCY:
This notice with comment
period announces the increase of certain
fees established under the Clinical
Laboratory Improvement Amendments
of 1988 (CLIA). The Public Health
Service Act (PHSA) requires the
Secretary to impose certificate fees to
cover the general costs of administering
the CLIA program, as well as additional
fees, including Inspection fees for nonaccredited laboratories. We are
increasing these fees to cover the cost of
administering the CLIA program as
required by statute. We seek public
comment regarding this increase, which
we believe is necessary to meet the
statutory requirements.
DATES: Comments: To be assured
consideration, comments must be
received at one of the addresses
provided below, no later than 5 p.m. on
March 1, 2019.
ADDRESSES: In commenting, refer to file
code CMS–3356–NC. Because of staff
and resource limitations, we cannot
khammond on DSK30JT082PROD with NOTICES
SUMMARY:
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accept comments by facsimile (FAX)
transmission.
Comments, including mass comment
submissions, must be submitted in one
of the following three ways (please
choose only one of the ways listed):
1. Electronically. You may submit
electronic comments on this regulation
to https://www.regulations.gov. Follow
the ‘‘Submit a comment’’ instructions.
2. By regular mail. You may mail
written comments to the following
address ONLY: Centers for Medicare &
Medicaid Services, Department of
Health and Human Services, Attention:
CMS–3356–NC, P.O. Box 8016,
Baltimore, MD 21244–8016. Please
allow sufficient time for mailed
comments to be received before the
close of the comment period.
3. By express or overnight mail. You
may send written comments to the
following address ONLY: Centers for
Medicare & Medicaid Services,
Department of Health and Human
Services, Attention: CMS–3356–NC,
Mail Stop C4–26–05, 7500 Security
Boulevard, Baltimore, MD 21244–1850.
For information on viewing public
comments, see the beginning of the
SUPPLEMENTARY INFORMATION section.
FOR FURTHER INFORMATION CONTACT: For
policy related questions, please contact
Cindy Flacks, 410–786–6520, and
Caecilia Blondiaux, 410–786–2190.
For the Budget and Financial Impact,
please contact Jeffrey Pleines, 410–786–
0684.
SUPPLEMENTARY INFORMATION:
Inspection of Public Comments: All
comments received before the close of
the comment period are available for
viewing by the public, including any
personally identifiable or confidential
business information that is included in
a comment. We post all comments
received before the close of the
comment period on the following
website as soon as possible after they
have been received: https://
www.regulations.gov. Follow the search
instructions on that website to view
public comments.
I. Background
A. CLIA Fees
On October 31, 1988, Congress
enacted the Clinical Laboratory
Improvement Amendments of 1988
(CLIA) (Pub. L. 100–578), which
replaced in its entirety section 353 of
the Public Health Service Act (PHSA).
Section 353(m) of the PHSA requires the
Secretary to impose two separate types
of fees: ‘‘certificate fees’’ and
‘‘additional fees.’’ Certificate fees are
imposed for the issuance and renewal of
certificates and must be sufficient to
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67723
cover the general costs of administering
the CLIA program, including evaluating
and monitoring approved proficiency
testing (PT) programs and accrediting
bodies and implementing and
monitoring compliance with program
requirements. Additional fees are
imposed for inspections of nonaccredited laboratories and for the cost
of performing PT on laboratories that do
not participate in approved PT programs
intended to cover the cost of evaluating
a laboratory to determine overall if an
accreditation organization’s standards
and inspection process is equivalent to
the CLIA program. These evaluations
are referred to as validation inspections.
The additional fees must be sufficient to
cover, among other things, the cost of
carrying out such inspections and PT.
Certificate and additional fees vary by
group or classification of laboratory,
based on such considerations as the
Secretary determines are relevant,
which may include the dollar volume
and scope of the testing being performed
by the laboratories, and only a nominal
fee may be required for the issuance and
renewal of Certificates of Waiver
(CoWs).
The regulations provide for a
methodology for determining fee
amounts (§ 493.649) and periodic
updating of the certificate fee amounts
(§ 493.638(b)) and compliance fee
amounts (§ 493.643(b)). Under
§ 493.645(b)(1), laboratories that are
issued a certificate of accreditation
(CoA) are assessed a fee to cover the cost
of validation inspections. All accredited
laboratories share in the cost of these
inspections. These costs are the same as
those that are incurred when inspecting
non-accredited laboratories.
B. CLIA Budget Process
With the exception of the ‘‘CLIA
Program; Fee Schedule Revision’’ notice
published in the August 29, 1997
Federal Register (62 FR 45815 through
45821), the fees imposed to cover the
costs of administering the CLIA program
have not been updated since 1992. The
fee amounts currently collected under
the CLIA regulations are based on
preliminary assumptions made in 1992
about future program operations and
workload requirements. After decades of
actual program experience, we have
determined that it is necessary to
increase certain CLIA fees to fund
current and future program operations
as required by section 353(m) of the
PHSA. Specifically, as discussed in
section II. of this notice with comment
period, we are increasing those CLIA
fees collected under § 493.638(b)
(hereinafter referred to as ‘‘Certificate
Fees’’), with the exception of fees for
E:\FR\FM\31DEN1.SGM
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Agencies
[Federal Register Volume 83, Number 249 (Monday, December 31, 2018)]
[Notices]
[Pages 67722-67723]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-27337]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-R-74]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Department of Health
and Human 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 (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 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 on the collection(s) of information must be received by
the OMB desk officer by January 30, 2019.
ADDRESSES: When commenting on the proposed information collections,
please reference the document identifier or OMB control number. To be
assured consideration, comments and recommendations must be received by
the OMB desk officer via one of the following transmissions: OMB,
Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number: (202) 395-5806 OR, Email: OIRA_
submission@omb.eop.gov.
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 Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at (410) 786-1326.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
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. 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 (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-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 that
summarizes the following proposed collection(s) of information for
public comment:
Information Collection
Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Income and
Eligibility Verification System Reporting and Supporting Regulations;
Use: Section 1137 of the Social Security Act requires that States
verify the income and eligibility information contained on the
applicant's application and in the applicant's case file through data
matches with the agencies and entities
[[Page 67723]]
identified in this section. The State Medicaid/CHIP agency will report
the existence of a system to collect all information needed to
determine and redetermine eligibility for Medicaid and CHIP. The State
Medicaid/CHIP agency will attest to using the PARIS system in
determining beneficiary eligibility in Medicaid or CHIP benefit
programs. Form Number: CMS-R-74 (OMB control number: 0938-0467);
Frequency: Occasionally; Affected Public: State, Local, or Tribal
Governments; Number of Respondents: 55; Total Annual Responses: 3,241;
Total Annual Hours: 1,071. (For policy questions regarding this
collection contact Stephanie Bell at 410-786-0617.)
Dated: December 13, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2018-27337 Filed 12-28-18; 8:45 am]
BILLING CODE 4120-01-P