Agency Information Collection Activities: Proposed Collection; Comment Request, 54352-54354 [2018-23576]
Download as PDF
54352
Federal Register / Vol. 83, No. 209 / Monday, October 29, 2018 / Notices
The annual burden for this
information collection is estimated to be
572,791 hours. This represents an
increase of 281,305 hours from the
current burden estimate of 291,486
hours. This increase is not due to any
new requirements imposed by the FDIC.
Rather, it is due to FDIC’s reassessment
of the burden hours associated with
responding to the existing requirements
of the Rule and to guidance, feedback,
and additional requests for information
by the FDIC as part of the iterative
resolution planning process. The
revised estimates are informed by
feedback received from the CIDIs over
the past year. Because submissions have
been required no more frequently than
biennially, the burden associated with
the Annual Update has been multiplied
by 2⁄3 to represent two Annual Update
filings over the three-year period
contemplated by this notice and
renewal.
Request for Comment
Comments are invited on: (a) Whether
the collection of information is
necessary for the proper performance of
the FDIC’s functions, including whether
the information has practical utility; (b)
the accuracy of the estimates of the
burden of the information collection,
including the validity of the
methodology and assumptions used; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (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. All comments will become
a matter of public record.
Dated at Washington, DC, on October 23,
2018.
Federal Deposit Insurance Corporation.
Robert E. Feldman,
Executive Secretary.
[FR Doc. 2018–23500 Filed 10–26–18; 8:45 am]
BILLING CODE 6714–01–P
FEDERAL ELECTION COMMISSION
Sunshine Act Meeting
amozie on DSK3GDR082PROD with NOTICES1
FEDERAL REGISTER CITATION NOTICE OF
PREVIOUS ANNOUNCEMENT: 83 FR 52832.
PREVIOUSLY ANNOUNCED TIME AND DATE OF
THE MEETING: Tuesday, October 23, 2018
at 10:00 a.m.
The meeting
was continued on Thursday, October 25,
2018.
*
*
*
*
*
CHANGES IN THE MEETING:
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CONTACT PERSON FOR MORE INFORMATION:
Judith Ingram, Press Officer, Telephone:
(202) 694–1220.
Laura E. Sinram,
Deputy Secretary of the Commission.
[FR Doc. 2018–23717 Filed 10–25–18; 4:15 pm]
BILLING CODE 6715–01–P
GENERAL SERVICES
ADMINISTRATION
[Notice MV–2018–01; Docket No. 2018–0002,
Sequence No. 29]
Federal Acquisition Regulation; FY
2019 FAR Reissue Posted to the
Acquisition.gov Website
General Services
Administration (GSA).
ACTION: Notice.
AGENCY:
This notice advises users that
the FY 2019 Federal Acquisition
Regulation (FAR) Reissue will be
available for download at https://
www.acquisition.gov/browsefar.
DATES: Applicable date: November 13,
2018.
SUMMARY:
The
Regulatory Secretariat Division, at 202–
501–4755; or via email at GSARegSec@
gsa.gov. Please cite 2019 FAR Reissue
Posted to the Acquisition.gov website.
SUPPLEMENTARY INFORMATION:
Periodically, the FAR is reissued
because of administrative necessity.
Although the reissue does not alter the
language of the FAR, it does contain
several administrative updates to
improve the user experience and
increase accessibility. The following
updates are to features that do not
appear in the Code of Federal
Regulations:
• Future Federal Acquisition
Circulars (FAC) will be renumbered so
that the next issued FAC will be FAC
2019–01. This reissue will replace the
prior numbering system which used
FACs 2005–01 through FAC 2005–101.
Because of the renumbering, the
Foreword section of the FAR will be
updated to reflect the current FAC
number.
• The FAR Looseleaf package will no
longer be offered. Instead, a List of
Sections Affected (LSA) will be
included on the https://acquisition.gov
website, and updated for each FAC.
• The matrix will continue to be
available in the PDF version of the FAR.
However, acquisition.gov will be
releasing the new Smart Matrix. The
new FAR Smart Matrix includes a
filterable clause matrix, file saving
options, improved search capabilities,
FOR FURTHER INFORMATION CONTACT:
PO 00000
Frm 00045
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Sfmt 4703
as well as hyperlinked clauses,
provisions and prescriptions to the
current version of the FAR.
• The FAR will be available in
HTML, XML, Word, and PDF formats.
Users intending to print the FAR can
refer to the Adobe PDF file.
• FAR Proposed Rule Publications
that are open for comments are available
at https://acquisition.gov/requesting_
comments.
• The Federal Alert Notices (FAN) are
available at https://acquisition.gov/fan_
list.
Although these changes do not alter
the Code of Federal Regulations, they
will provide smoother access to the FAR
for new and experienced users alike.
Please contact the Regulatory Secretariat
Division with any questions or
concerns.
Dated: October 24, 2018.
William F. Clark,
Director, Office of Government-wide
Acquisition Policy, Office of Acquisition
Policy, Office of Government-wide Policy.
[FR Doc. 2018–23568 Filed 10–26–18; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10492, CMS–
10664, and CMS–R–74]
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 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
SUMMARY:
E:\FR\FM\29OCN1.SGM
29OCN1
Federal Register / Vol. 83, No. 209 / Monday, October 29, 2018 / Notices
amozie on DSK3GDR082PROD with NOTICES1
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
December 28, 2018.
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 ll, 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 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–10492 Data Submission for the
Federally-facilitated Exchange User
Fee Adjustment
CMS–10664 Medicare Durable Medical
Equipment, Prosthetics, Orthotics,
and Supplies (DMEPOS) Templates
CMS–R–74 Income and Eligibility
Verification System Reporting and
Supporting Regulations
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
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17:48 Oct 26, 2018
Jkt 247001
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: Extension without change of a
currently approved collection; Title of
Information Collection: Data
Submission for the Federally-facilitated
Exchange User Fee Adjustment; Use:
Section 2713 of the Public Health
Service Act requires coverage without
cost sharing of certain preventive health
services, including certain contraceptive
services, in non-exempt, nongrandfathered group health plans and
health insurance coverage. The final
regulations establish rules under which
the third party administrator of the plan
would provide or arrange for a third
party to provide separate contraceptive
coverage to plan participants and
beneficiaries without cost sharing,
premium, fee, or other charge to plan
participants or beneficiaries or to the
eligible organization or its plan. Eligible
organizations are required to self-certify
that they are eligible for this
accommodation and provide a copy of
such self-certification to their third
party administrators. The final rules
also set forth processes and standards to
fund the payments for the contraceptive
services that are provided for
participants and beneficiaries in selfinsured plans of eligible organizations
under the accommodation described
previously, through an adjustment in
the FFE user fee payable by an issuer
participating in an FFE.
CMS will use the data collections
from participating issuers and third
party administrators to verify the total
dollar amount for such payments for
contraceptive services provided under
this accommodation for the purpose of
determining a participating issuer’s user
fee adjustment. The attestation that the
payments for contraceptive services
were made in compliance with 26 CFR
54.9815–2713A(b)(2) or 29 CFR
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Frm 00046
Fmt 4703
Sfmt 4703
54353
2590.715–2713A(b)(2) will help ensure
that the user fee adjustment is being
utilized to provide contraceptive
services for the self-insured plans in
accordance with the previously noted
accommodation. Form Number: CMS–
10492 (OMB control number: 0938–
1285); Frequency: Annually; Affected
Public: Private sector (Business or other
for-profits and Not-for-profit
institutions); Number of Respondents:
861; Total Annual Responses: 861; Total
Annual Hours: 12,930. (For policy
questions regarding this collection
contact Ernest Ayukawa (301) 492–
5213.)
2. Type of Information Collection
Request: New collection (Request for a
new OMB Control Number); Title of
Information Collection: Medicare
Durable Medical Equipment,
Prosthetics, Orthotics, and Supplies
(DMEPOS) Templates; Use: The
templates will help users capture the
appropriate information needed to
document medical necessity and
appropriateness to help qualify
DMEPOS for reimbursement under
Medicare coverage and payment
regulations. The physicians/NPPs
complete the DMEPOS F2F encounter
documentation or progress note, the
DMEPOS order, and the results of
required laboratory testing. This will
help physicians/NPPs in complying
with Medicare policy requirements,
thereby reducing improper payments
secondary to insufficient
documentation. In addition, CMS will
use this information to help substantiate
that the request for payment (e.g. claim)
is for devices and services that are
medically necessary and appropriate as
required by regulation. This will
substantially reduce inappropriate
payment due to incomplete
documentation.
The primary users of these clinical
templates will be physicians/NPPs and
their support staff. The users of the
information will also include other
providers and suppliers that must have
documentation to substantiate the need
for the devices or services as part of the
requirements for payment by Medicare
FFS. Complete documentation will help
with reducing claim denials and
improper payments. By using these
templates and CDEs, providers and
suppliers of DMEPOS devices and
services will receive proper
documentation/information from the
referring provider that is required for
payment. Form Number: CMS–10664
(OMB control number: 0938–NEW);
Frequency: Annually; Affected Public:
Private Sector, Business or other forprofit and not-for-profit institutions;
Number of Respondents: 522; Number
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54354
Federal Register / Vol. 83, No. 209 / Monday, October 29, 2018 / Notices
of Responses: 2,138; Total Annual
Hours: 170,589. (For policy questions
regarding this collection contact Kevin
Young at 410–786–6133 or Ashley
Stedding at 410–786–4250).
3. 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
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: October 23, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–23576 Filed 10–26–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10494]
Agency Information Collection
Activities: Submission for OMB
Review; 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
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
amozie on DSK3GDR082PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:48 Oct 26, 2018
Jkt 247001
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.
Comments on the collection(s) of
information must be received by the
OMB desk officer by November 28,
2018.
DATES:
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.hhs.gov/Paperwork
ReductionActof1995.
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
ADDRESSES:
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
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:
1. Type of Information Collection
Request: Revision of a previously
approved collection; Title of
Information Collection: Exchange
Functions: Standards for Navigators and
Non-Navigator Assistance Personnel—
CAC; Use: Section 1321(a)(1) of the
Affordable Care Act directs and
authorizes the Secretary to issue
regulations setting standards for meeting
the requirements under title I of the
Affordable Care Act, with respect to,
among other things, the establishment
and operation of Exchanges. Pursuant to
this authority, regulations establishing
the certified application counselor
program have been finalized at 45 CFR
155.225. In accordance with
155.225(d)(1) and (7), certified
application counselors in all Exchanges
are required to be initially certified and
recertified on at least an annual basis
and successfully complete Exchangerequired training. Form Number: CMS–
10494 (OMB control number: 0938–
1205); Frequency: On Occasion;
Affected Public: State, Local, or Tribal
Governments, Private Sector (not-forprofit institutions); individuals or
households; Number of Respondents:
30,000; Total Annual Responses:
30,000; Total Annual Hours: 7,500. (For
policy questions regarding this
collection contact Deborah Bryant at
301–492–5213.)
Dated: October 24, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–23590 Filed 10–26–18; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects: Office of Child
Care CCDF Onsite Monitoring.
Title: Child Care and Development
Fund (CCDF) State Monitoring
Compliance Demonstration Packet.
OMB No.: New.
E:\FR\FM\29OCN1.SGM
29OCN1
Agencies
[Federal Register Volume 83, Number 209 (Monday, October 29, 2018)]
[Notices]
[Pages 54352-54354]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-23576]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10492, CMS-10664, and CMS-R-74]
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 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
[[Page 54353]]
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 December 28, 2018.
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 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-10492 Data Submission for the Federally-facilitated Exchange User
Fee Adjustment
CMS-10664 Medicare Durable Medical Equipment, Prosthetics, Orthotics,
and Supplies (DMEPOS) Templates
CMS-R-74 Income and Eligibility Verification System Reporting and
Supporting 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: Extension without change
of a currently approved collection; Title of Information Collection:
Data Submission for the Federally-facilitated Exchange User Fee
Adjustment; Use: Section 2713 of the Public Health Service Act requires
coverage without cost sharing of certain preventive health services,
including certain contraceptive services, in non-exempt, non-
grandfathered group health plans and health insurance coverage. The
final regulations establish rules under which the third party
administrator of the plan would provide or arrange for a third party to
provide separate contraceptive coverage to plan participants and
beneficiaries without cost sharing, premium, fee, or other charge to
plan participants or beneficiaries or to the eligible organization or
its plan. Eligible organizations are required to self-certify that they
are eligible for this accommodation and provide a copy of such self-
certification to their third party administrators. The final rules also
set forth processes and standards to fund the payments for the
contraceptive services that are provided for participants and
beneficiaries in self-insured plans of eligible organizations under the
accommodation described previously, through an adjustment in the FFE
user fee payable by an issuer participating in an FFE.
CMS will use the data collections from participating issuers and
third party administrators to verify the total dollar amount for such
payments for contraceptive services provided under this accommodation
for the purpose of determining a participating issuer's user fee
adjustment. The attestation that the payments for contraceptive
services were made in compliance with 26 CFR 54.9815-2713A(b)(2) or 29
CFR 2590.715-2713A(b)(2) will help ensure that the user fee adjustment
is being utilized to provide contraceptive services for the self-
insured plans in accordance with the previously noted accommodation.
Form Number: CMS-10492 (OMB control number: 0938-1285); Frequency:
Annually; Affected Public: Private sector (Business or other for-
profits and Not-for-profit institutions); Number of Respondents: 861;
Total Annual Responses: 861; Total Annual Hours: 12,930. (For policy
questions regarding this collection contact Ernest Ayukawa (301) 492-
5213.)
2. Type of Information Collection Request: New collection (Request
for a new OMB Control Number); Title of Information Collection:
Medicare Durable Medical Equipment, Prosthetics, Orthotics, and
Supplies (DMEPOS) Templates; Use: The templates will help users capture
the appropriate information needed to document medical necessity and
appropriateness to help qualify DMEPOS for reimbursement under Medicare
coverage and payment regulations. The physicians/NPPs complete the
DMEPOS F2F encounter documentation or progress note, the DMEPOS order,
and the results of required laboratory testing. This will help
physicians/NPPs in complying with Medicare policy requirements, thereby
reducing improper payments secondary to insufficient documentation. In
addition, CMS will use this information to help substantiate that the
request for payment (e.g. claim) is for devices and services that are
medically necessary and appropriate as required by regulation. This
will substantially reduce inappropriate payment due to incomplete
documentation.
The primary users of these clinical templates will be physicians/
NPPs and their support staff. The users of the information will also
include other providers and suppliers that must have documentation to
substantiate the need for the devices or services as part of the
requirements for payment by Medicare FFS. Complete documentation will
help with reducing claim denials and improper payments. By using these
templates and CDEs, providers and suppliers of DMEPOS devices and
services will receive proper documentation/information from the
referring provider that is required for payment. Form Number: CMS-10664
(OMB control number: 0938-NEW); Frequency: Annually; Affected Public:
Private Sector, Business or other for-profit and not-for-profit
institutions; Number of Respondents: 522; Number
[[Page 54354]]
of Responses: 2,138; Total Annual Hours: 170,589. (For policy questions
regarding this collection contact Kevin Young at 410-786-6133 or Ashley
Stedding at 410-786-4250).
3. 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 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: October 23, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2018-23576 Filed 10-26-18; 8:45 am]
BILLING CODE 4120-01-P