Agency Information Collection Activities: Submission for OMB Review; Comment Request, 47343-47345 [2018-20372]
Download as PDF
Federal Register / Vol. 83, No. 182 / Wednesday, September 19, 2018 / Notices
of Offeror, requires each offeror to
identify if the offeror is, within the last
three years, a successor to another entity
that received a Federal Government
award and, if so, to provide the
Commercial and Government Entity
(CAGE) code and legal name of the
predecessor. The information on
predecessors is used to identify such
entities in the Federal Awardee
Performance and Integrity Information
System (FAPIIS) to allow retrieval of
integrity and performance data on the
most recent predecessor of an apparent
successful offeror to whom award is
anticipated. FAR 9.104–6 requires
contracting officers to consult FAPIIS
before awarding a contract in excess of
the simplified acquisition threshold.
The information on predecessors is
collected on an annual basis for
inclusion in the annual representations
and certifications in the System for
Award Management (SAM) for offerors
required to register in SAM. Offerors not
required to register in SAM but required
to provide the information in the
provision at FAR 52.204–20 will do so
as specified in the solicitation or
instructed by the contracting officer.
amozie on DSK3GDR082PROD with NOTICES1
C. Annual Reporting Burden
The burden to provide the
information required by the FAR
provision at 52.204–20 when an offeror
is registered in SAM is already covered
by OMB Control Number 9000–0159,
System for Award Management
Registration (SAM). OMB Control
Number 9000–0189 now will cover the
burden for providing the required
information when the offeror is not
required to register in SAM in
accordance with the exceptions in FAR
4.1102(a). The Federal Procurement
Data System (FPDS) for FY 2017 was
used to develop the estimated burden
hours as shown below:
Respondents: 974.
Responses Per Respondent: 1.
Total Annual Responses: 974.
Hours Per Response: 0.1.
Total Burden Hours: 97.4.
Affected Public: Businesses or other
for-profit and not-for-profit institutions.
Obtaining Copies: Requesters may
obtain a copy of the information
collection documents from the General
Services Administration, Regulatory
Secretariat Division (MVCB), 1800 F
Street NW, Washington, DC 20405,
telephone 202–501–4755. Please cite
OMB Control No. 9000–0189,
Identification of Predecessors, in all
correspondence.
VerDate Sep<11>2014
17:09 Sep 18, 2018
Jkt 244001
Dated: September 13, 2018.
William Clark,
Director, Office of Governmentwide
Acquisition Policy, Office of Acquisition
Policy, Office of Governmentwide Policy.
[FR Doc. 2018–20299 Filed 9–18–18; 8:45 am]
BILLING CODE 6820–EP–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10673]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Department of
Health and Human Services.
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
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 October 19, 2018.
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.
DATES:
PO 00000
Frm 00016
Fmt 4703
Sfmt 4703
47343
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
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: New Collection (Request for a
new OMB control number); Title of
Information Collection: Medicare
Advantage Qualifying Payment
Arrangement Incentive (MAQI)
Demonstration; Use: The Centers for
Medicare & Medicaid Services (CMS)
may test a demonstration, under Section
402 of the Social Security Amendments
of 1968 (as amended), entitled the
Medicare Advantage Qualifying
Payment Arrangement Incentive (MAQI)
Demonstration (‘‘the Demonstration’’). If
it goes forward, the MAQI
demonstration could test whether
exempting, through the use of waiver
authority, clinicians who participate to
a sufficient degree in certain payment
arrangements with Medicare Advantage
Organizations (MAOs) (combined with
participation, if any, in Advanced
Alternative Payment Models (APMs)
with Medicare Fee-for-Service (FFS))
from the Merit-based Incentive Payment
System (MIPS) reporting requirements
E:\FR\FM\19SEN1.SGM
19SEN1
amozie on DSK3GDR082PROD with NOTICES1
47344
Federal Register / Vol. 83, No. 182 / Wednesday, September 19, 2018 / Notices
and payment adjustment will increase
or maintain participation in payment
arrangements with MAOs similar to
Advanced APMs and change the
manner in which clinicians deliver care.
Clinicians may currently participate
in one of two paths of the Quality
Payment Program (QPP): (1) MIPS,
which adjusts Medicare payments based
on combined performance on measures
of quality, cost, improvement activities,
and advancing care information, or (2)
Advanced Alternative Payment Models
with Medicare (Advanced APMs), under
which eligible clinicians may earn an
incentive payment for sufficient
participation in certain payment
arrangements with Medicare fee-forservice (FFS) and other payers, and
starting in the 2019 performance period,
with other payers such as Medicare
Advantage, commercial payers, and
Medicaid managed care. To participate
in the Advanced APM path of QPP for
a given year, eligible clinicians must
meet the criteria of Qualifying APM
Participants (QPs); in addition to
earning an APM incentive payment, QPs
are excluded from the MIPS reporting
requirements and payment adjustment.
An eligible clinician that does not
meet the criteria to be a QP for a given
year will be subject to MIPS for that year
unless the clinician meets certain other
MIPS exclusion criteria, such as being
newly enrolled in Medicare or meeting
the low volume threshold for Medicare
FFS patients. The MAQI Demonstration
could allow participating clinicians to
have the opportunity to be exempt from
MIPS reporting and payment
consequences for a given year if they
participate to a sufficient degree in
certain Qualifying Payment
Arrangements with MAOs (and
Advanced APMs with Medicare FFS)
during the performance period for that
year, without requiring them to be QPs
or otherwise meet the MIPS exclusion
criteria of QPP. Under a possible
Demonstration, clinicians might not be
required to have a minimum amount of
participation in an Advanced APM with
Medicare FFS in order to be exempt
from MIPS reporting requirements and
payment adjustments for a year, but if
they did have participation in Advanced
APMs with Medicare FFS, that
participation could also be counted
towards the thresholds that trigger the
waiver from MIPS reporting and
payment consequences. In addition, the
Demonstration could permit
consideration of participation in
‘‘Qualifying Payment Arrangements’’
with Medicare Advantage plans that
meet the criteria to be Other Payer
Advanced APMs a year before the AllPayer Combination Option is available.
VerDate Sep<11>2014
17:09 Sep 18, 2018
Jkt 244001
In the Calendar Year 2018 Quality
Payment Program Final Rule, CMS
noted its intention ‘‘to develop a
demonstration project to test the effects
of expanding incentives for eligible
clinicians to participate in innovative
alternative payment arrangements under
Medicare Advantage that qualify as
Advanced APMs, by allowing credit for
participation in such Medicare
Advantage arrangements prior to 2019
and incentivizing participation in such
arrangements in 2018 through 2024.’’
(92 FR 53865).
The first performance period for the
Demonstration is tentatively planned for
2018 and the Demonstration would last
up to five years. Clinicians who meet
the definition of MIPS eligible clinician
under QPP as defined under 42 CFR
414.1305 would be eligible to
participate in the MAQI Demonstration.
Currently, MIPS eligible clinicians
include physicians (including doctors of
medicine, doctors of osteopathy,
osteopathic practitioners, doctors of
dental surgery, doctors of dental
medicine, doctors of podiatric medicine,
doctors of optometry, and
chiropractors), physician assistants,
nurse practitioners, clinical nurse
specialists, and certified registered
nurse anesthetists. If the definition of
MIPS eligible clinician changes under
future rulemaking, the Demonstration
would use the updated definition to
define Demonstration eligibility.
Participation could last the duration
of the Demonstration, unless
participation is voluntarily or
involuntarily terminated under the
terms and conditions of the
Demonstration. Participants would have
the opportunity to submit the required
documentation and be evaluated for
MIPS waivers through the
Demonstration each year.
Should this demonstration move
forward, and in order to conduct an
evaluation and effectively implement
the MAQI Demonstration, CMS would
need to collect information from
Demonstration participants on (a)
payment arrangements with MAOs and
(b) Medicare Advantage (MA) payments
and patient counts. CMS would require
a new collection of this information as
this information is not already available
through other sources and/or has not
been previously approved for use under
the MAQI Demonstration. The
information collected in these forms
would allow CMS to evaluate whether
the payment arrangement that clinicians
have with MAOs meet the Qualifying
Payment Arrangement criteria, and
determine whether a clinician’s MAO
and FFS APM patient population or
payments meet demonstration
PO 00000
Frm 00017
Fmt 4703
Sfmt 4703
thresholds. Both of these areas are also
requirements for review and data
collection under QPP (i.e. the Eligible
Clinician-Initiated Other Payer
Advanced APM Determination form and
All-Payer QP Submission form), and
therefore similar to forms have been
prepared and reviewed under the QPP.
Given these similarities in forms,
burden estimates for the MAQI
Demonstration PRA package were
derived from burden analyses and
formulation done in conjunction with
the QPP forms; more specifically the
estimated burden associated with the
submission of payment arrangement
information for Other Payer Advanced
APM Determinations: Eligible ClinicianInitiated Process, and the estimated
burden associated with the submission
of data for All-Payer QP determinations.
CMS estimates the total hour burden per
respondent for the MAQI demonstration
to be 15 hours, to match the hours listed
in the equivalent QPP forms. Full detail
of how these estimates were derived can
be found in the forthcoming Calendar
Year 2019 Proposed QPP rule.
If Demonstration participants
submitted information, but did not meet
these conditions of the Demonstration,
their participation in the Demonstration
would not be terminated, but they
would not receive the waivers from
MIPS reporting requirements and
payment adjustments. Therefore, unless
they become QPs or are excluded from
MIPS for other reasons, the participating
clinicians would be subject to MIPS and
would face the MIPS payment
adjustments for the applicable year. We
are requesting approval of 2 information
collections associated with the MAQI
Demonstration: (a) A Qualifying
Payment Arrangement Submission Form
and (b) a Threshold Data Submission
Form. Subsequent to publishing the 60day Federal Register notice (83 FR
31150), there have been minor revisions
made to the collection instrument to
clarify information. There is no increase
in the burden hours. Form Number:
CMS–10673 (OMB control number:
0938–NEW); Frequency: Annually;
Affected Public: Private sector—
Business or other for-profit and Not-forprofit institutions; Number of
Respondents: 100,000; Total Annual
Responses: 100,000; Total Annual
Hours: 1,500,000. (For policy questions
regarding this collection contact John
Amoh at john.amoh@cms.hhs.gov.)
E:\FR\FM\19SEN1.SGM
19SEN1
Federal Register / Vol. 83, No. 182 / Wednesday, September 19, 2018 / Notices
Dated: September 14, 2018.
Martique Jones,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–20372 Filed 9–18–18; 8:45 am]
U.S. Customs and Border Protection
[1651–0029]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency Information Collection
Activities: Application for ForeignTrade Zone Admission and/or Status
Designation, and Application for
Foreign-Trade Zone Activity Permit
Food and Drug Administration
AGENCY:
BILLING CODE 4120–01–P
U.S. Customs and Border
Protection (CBP), Department of
Homeland Security.
ACTION: 30-Day notice and request for
comments; extension of an existing
collection of information.
[Docket No. FDA–2018–D–3152]
Postapproval Changes to Drug
Substances; Draft Guidance for
Industry; Availability; Correction
AGENCY:
Notice; correction.
The Food and Drug
Administration is correcting a notice
entitled ‘‘Postapproval Changes to Drug
Substances; Draft Guidance for Industry;
Availability’’ that appeared in the
Federal Register of September 11, 2018.
The document announced a draft
guidance that provides
recommendations to holders of
approved new drug applications,
abbreviated new drug applications, new
animal drug applications, abbreviated
new animal drug applications, and
holders of drug master files and
veterinary master files who may want to
make a change to the drug substance
manufacturing process during the drug
product application postapproval
period. The document was published
with the incorrect docket number. This
document corrects that error.
FOR FURTHER INFORMATION CONTACT: Lisa
Granger, Office of Policy and Planning,
Food and Drug Administration, 10903
New Hampshire Ave., Bldg. 32, Rm.
3330, Silver Spring, MD 20993–0002,
301–796–9115.
SUPPLEMENTARY INFORMATION: In the
Federal Register of Tuesday, September
11, 2018 (83 FR 45944), in FR Doc.
2018–19666, on page 45944, the
following correction is made:
On page 45944, in the first column, in
the header of the document, and also in
the third column under Instructions,
‘‘Docket No. FDA–2018–D–3151’’ is
corrected to read ‘‘Docket No. FDA–
2018–D–3152’’.
SUMMARY:
Dated: September 12, 2018.
Leslie Kux,
Associate Commissioner for Policy.
[FR Doc. 2018–20317 Filed 9–18–18; 8:45 am]
BILLING CODE 4164–01–P
VerDate Sep<11>2014
17:09 Sep 18, 2018
Jkt 244001
The Department of Homeland
Security, U.S. Customs and Border
Protection will be submitting the
following information collection request
to the Office of Management and Budget
(OMB) for review and approval in
accordance with the Paperwork
Reduction Act of 1995 (PRA). The
information collection is published in
the Federal Register to obtain comments
from the public and affected agencies.
Comments are encouraged and will be
accepted no later than October 19, 2018
to be assured of consideration.
ADDRESSES: Interested persons are
invited to submit written comments on
this proposed information collection to
the Office of Information and Regulatory
Affairs, Office of Management and
Budget. Comments should be addressed
to the OMB Desk Officer for Customs
and Border Protection, Department of
Homeland Security, and sent via
electronic mail to dhsdeskofficer@
omb.eop.gov.
SUMMARY:
Food and Drug Administration,
HHS
ACTION:
amozie on DSK3GDR082PROD with NOTICES1
DEPARTMENT OF HOMELAND
SECURITY
FOR FURTHER INFORMATION CONTACT:
Requests for additional PRA information
should be directed to Seth Renkema,
Chief, Economic Impact Analysis
Branch, U.S. Customs and Border
Protection, Office of Trade, Regulations
and Rulings, 90 K Street NE, 10th Floor,
Washington, DC 20229–1177,
Telephone number (202) 325–0056 or
via email CBP_PRA@cbp.dhs.gov. Please
note that the contact information
provided here is solely for questions
regarding this notice. Individuals
seeking information about other CBP
programs should contact the CBP
National Customer Service Center at
877–227–5511, (TTY) 1–800–877–8339,
or CBP website at https://www.cbp
.gov/.
SUPPLEMENTARY INFORMATION: CBP
invites the general public and other
Federal agencies to comment on the
proposed and/or continuing information
collections pursuant to the Paperwork
PO 00000
Frm 00018
Fmt 4703
Sfmt 4703
47345
Reduction Act of 1995 (44 U.S.C. 3501
et seq.). This proposed information
collection was previously published in
the Federal Register (Volume 83 FR
Page 23286) on May 18, 2018, allowing
for a 60-day comment period. This
notice allows for an additional 30 days
for public comments. This process is
conducted in accordance with 5 CFR
1320.8. Written comments and
suggestions from the public and affected
agencies should address one or more of
the following four points: (1) 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; (2) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
suggestions to enhance the quality,
utility, and clarity of the information to
be collected; and (4) suggestions to
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. The
comments that are submitted will be
summarized and included in the request
for approval. All comments will become
a matter of public record.
Overview of This Information
Collection
Title: Application for Foreign-Trade
Zone Admission and/or Status
Designation, and Application for
Foreign-Trade Zone Activity Permit.
OMB Number: 1651–0029.
Form Numbers: 214, 214A, 214B,
214C, and 216.
Type of Review: Extension (without
change).
Action: CBP proposes to extend the
expiration date of this information
collection with no change to the burden
hours or to CBP Forms 214, 214A, 214B,
214C, and 216.
Affected Public: Businesses.
Abstract: Foreign trade zones (FTZs)
are geographical enclaves located within
the geographical limits of the United
States but for tariff purposes are
considered to be outside the United
States. Imported merchandise may be
brought into FTZs for storage,
manipulation, manufacture or other
processing and subsequent removal for
exportation, consumption in the United
States, or destruction. A company
bringing goods into an FTZ has a choice
of zone status (privileged/nonprivileged foreign, domestic, or zone-
E:\FR\FM\19SEN1.SGM
19SEN1
Agencies
[Federal Register Volume 83, Number 182 (Wednesday, September 19, 2018)]
[Notices]
[Pages 47343-47345]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-20372]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10673]
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 October 19, 2018.
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:
[email protected].
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/PaperworkReductionActof1995.
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: 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:
1. Type of Information Collection Request: New Collection (Request
for a new OMB control number); Title of Information Collection:
Medicare Advantage Qualifying Payment Arrangement Incentive (MAQI)
Demonstration; Use: The Centers for Medicare & Medicaid Services (CMS)
may test a demonstration, under Section 402 of the Social Security
Amendments of 1968 (as amended), entitled the Medicare Advantage
Qualifying Payment Arrangement Incentive (MAQI) Demonstration (``the
Demonstration''). If it goes forward, the MAQI demonstration could test
whether exempting, through the use of waiver authority, clinicians who
participate to a sufficient degree in certain payment arrangements with
Medicare Advantage Organizations (MAOs) (combined with participation,
if any, in Advanced Alternative Payment Models (APMs) with Medicare
Fee-for-Service (FFS)) from the Merit-based Incentive Payment System
(MIPS) reporting requirements
[[Page 47344]]
and payment adjustment will increase or maintain participation in
payment arrangements with MAOs similar to Advanced APMs and change the
manner in which clinicians deliver care.
Clinicians may currently participate in one of two paths of the
Quality Payment Program (QPP): (1) MIPS, which adjusts Medicare
payments based on combined performance on measures of quality, cost,
improvement activities, and advancing care information, or (2) Advanced
Alternative Payment Models with Medicare (Advanced APMs), under which
eligible clinicians may earn an incentive payment for sufficient
participation in certain payment arrangements with Medicare fee-for-
service (FFS) and other payers, and starting in the 2019 performance
period, with other payers such as Medicare Advantage, commercial
payers, and Medicaid managed care. To participate in the Advanced APM
path of QPP for a given year, eligible clinicians must meet the
criteria of Qualifying APM Participants (QPs); in addition to earning
an APM incentive payment, QPs are excluded from the MIPS reporting
requirements and payment adjustment.
An eligible clinician that does not meet the criteria to be a QP
for a given year will be subject to MIPS for that year unless the
clinician meets certain other MIPS exclusion criteria, such as being
newly enrolled in Medicare or meeting the low volume threshold for
Medicare FFS patients. The MAQI Demonstration could allow participating
clinicians to have the opportunity to be exempt from MIPS reporting and
payment consequences for a given year if they participate to a
sufficient degree in certain Qualifying Payment Arrangements with MAOs
(and Advanced APMs with Medicare FFS) during the performance period for
that year, without requiring them to be QPs or otherwise meet the MIPS
exclusion criteria of QPP. Under a possible Demonstration, clinicians
might not be required to have a minimum amount of participation in an
Advanced APM with Medicare FFS in order to be exempt from MIPS
reporting requirements and payment adjustments for a year, but if they
did have participation in Advanced APMs with Medicare FFS, that
participation could also be counted towards the thresholds that trigger
the waiver from MIPS reporting and payment consequences. In addition,
the Demonstration could permit consideration of participation in
``Qualifying Payment Arrangements'' with Medicare Advantage plans that
meet the criteria to be Other Payer Advanced APMs a year before the
All-Payer Combination Option is available.
In the Calendar Year 2018 Quality Payment Program Final Rule, CMS
noted its intention ``to develop a demonstration project to test the
effects of expanding incentives for eligible clinicians to participate
in innovative alternative payment arrangements under Medicare Advantage
that qualify as Advanced APMs, by allowing credit for participation in
such Medicare Advantage arrangements prior to 2019 and incentivizing
participation in such arrangements in 2018 through 2024.'' (92 FR
53865).
The first performance period for the Demonstration is tentatively
planned for 2018 and the Demonstration would last up to five years.
Clinicians who meet the definition of MIPS eligible clinician under QPP
as defined under 42 CFR 414.1305 would be eligible to participate in
the MAQI Demonstration. Currently, MIPS eligible clinicians include
physicians (including doctors of medicine, doctors of osteopathy,
osteopathic practitioners, doctors of dental surgery, doctors of dental
medicine, doctors of podiatric medicine, doctors of optometry, and
chiropractors), physician assistants, nurse practitioners, clinical
nurse specialists, and certified registered nurse anesthetists. If the
definition of MIPS eligible clinician changes under future rulemaking,
the Demonstration would use the updated definition to define
Demonstration eligibility.
Participation could last the duration of the Demonstration, unless
participation is voluntarily or involuntarily terminated under the
terms and conditions of the Demonstration. Participants would have the
opportunity to submit the required documentation and be evaluated for
MIPS waivers through the Demonstration each year.
Should this demonstration move forward, and in order to conduct an
evaluation and effectively implement the MAQI Demonstration, CMS would
need to collect information from Demonstration participants on (a)
payment arrangements with MAOs and (b) Medicare Advantage (MA) payments
and patient counts. CMS would require a new collection of this
information as this information is not already available through other
sources and/or has not been previously approved for use under the MAQI
Demonstration. The information collected in these forms would allow CMS
to evaluate whether the payment arrangement that clinicians have with
MAOs meet the Qualifying Payment Arrangement criteria, and determine
whether a clinician's MAO and FFS APM patient population or payments
meet demonstration thresholds. Both of these areas are also
requirements for review and data collection under QPP (i.e. the
Eligible Clinician-Initiated Other Payer Advanced APM Determination
form and All-Payer QP Submission form), and therefore similar to forms
have been prepared and reviewed under the QPP.
Given these similarities in forms, burden estimates for the MAQI
Demonstration PRA package were derived from burden analyses and
formulation done in conjunction with the QPP forms; more specifically
the estimated burden associated with the submission of payment
arrangement information for Other Payer Advanced APM Determinations:
Eligible Clinician-Initiated Process, and the estimated burden
associated with the submission of data for All-Payer QP determinations.
CMS estimates the total hour burden per respondent for the MAQI
demonstration to be 15 hours, to match the hours listed in the
equivalent QPP forms. Full detail of how these estimates were derived
can be found in the forthcoming Calendar Year 2019 Proposed QPP rule.
If Demonstration participants submitted information, but did not
meet these conditions of the Demonstration, their participation in the
Demonstration would not be terminated, but they would not receive the
waivers from MIPS reporting requirements and payment adjustments.
Therefore, unless they become QPs or are excluded from MIPS for other
reasons, the participating clinicians would be subject to MIPS and
would face the MIPS payment adjustments for the applicable year. We are
requesting approval of 2 information collections associated with the
MAQI Demonstration: (a) A Qualifying Payment Arrangement Submission
Form and (b) a Threshold Data Submission Form. Subsequent to publishing
the 60-day Federal Register notice (83 FR 31150), there have been minor
revisions made to the collection instrument to clarify information.
There is no increase in the burden hours. Form Number: CMS-10673 (OMB
control number: 0938-NEW); Frequency: Annually; Affected Public:
Private sector--Business or other for-profit and Not-for-profit
institutions; Number of Respondents: 100,000; Total Annual Responses:
100,000; Total Annual Hours: 1,500,000. (For policy questions regarding
this collection contact John Amoh at [email protected].)
[[Page 47345]]
Dated: September 14, 2018.
Martique Jones,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. 2018-20372 Filed 9-18-18; 8:45 am]
BILLING CODE 4120-01-P