Agency Information Collection Activities: Proposed Collection; Comment Request, 48030-48032 [2022-16869]
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individuals who have the expertise and
qualifications necessary to contribute to
the accomplishment of the Study
Section’s objectives. Nominees will be
selected based on expertise in the fields
of occupational medicine and nursing,
industrial hygiene, occupational safety
and engineering, toxicology, chemistry,
safety and health education,
ergonomics, epidemiology, economic
science, psychology, pulmonary
pathology/physiology, and social
science. Federal employees will not be
considered for membership. Members
may be invited to serve for up to fouryear terms.
Selection of members is based on
candidates’ qualifications to contribute
to the accomplishment of SOHSS
objectives.
The U.S. Department of Health and
Human Services (HHS) policy stipulates
that committee membership be balanced
in terms of points of view represented,
and the Study Section’s function.
Appointments shall be made without
discrimination on the basis of age, race,
ethnicity, gender, sexual orientation,
gender identity, HIV status, disability,
and cultural, religious, or
socioeconomic status. Nominees must
be U.S. citizens and cannot be full-time
employees of the U.S. Government.
Current participation on federal
workgroups or prior experience serving
on a federal advisory committee does
not disqualify a candidate; however,
HHS policy is to avoid excessive
individual service on advisory
committees and multiple committee
memberships. CDC reviews potential
candidates for SOHSS membership each
year and provides a slate of nominees
for consideration to the Secretary of
HHS for final selection. HHS notifies
selected candidates of their
appointment near the start of the term
in October 2023, or as soon as the HHS
selection process is completed. Note
that the need for different expertise
varies from year to year and a candidate
who is not selected in one year may be
reconsidered in a subsequent year.
Candidates should submit the following
items:
D Current curriculum vitae, including
complete contact information
(telephone numbers, mailing address,
email address).
D At least one letter of
recommendation from person(s) not
employed by the U.S. Department of
Health and Human Services. Candidates
may submit letter(s) from current HHS
employees if they wish, but at least one
letter must be submitted by a person not
employed by an HHS agency (e.g., CDC,
NIH, FDA).
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Nominations may be submitted by the
candidate or by the person/organization
recommending the candidate.
The Director, Strategic Business
Initiatives Unit, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Strategic Business Initiatives Unit,
Office of the Chief Operating Officer, Centers
for Disease Control and Prevention.
[FR Doc. 2022–16807 Filed 8–4–22; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10003, CMS–
1771, CMS–R–244 and CMS–10744]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
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
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
October 4, 2022.
SUMMARY:
PO 00000
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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: lll, 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
website address at https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
FOR FURTHER INFORMATION CONTACT:
William N. Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
ADDRESSES:
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–10003—Notice of Denial of
Medical Coverage (or Payment)
CMS–1771—Emergency and Foreign
Hospital Services and Supporting
Regulation in 42 CFR Section 424.103
CMS–R–244—Programs of All-Inclusive
Care for the Elderly (PACE)
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
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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 of a currently
approved collection; Title: Notice of
Denial of Medical Coverage (or
Payment); Use: Section 1852(g)(1)(B) of
the Social Security Act (the Act)
requires Medicare health plans to
provide enrollees with a written notice
in understandable language of the
reasons for the denial and a description
of the applicable appeals processes.
Medicare health plans, including
Medicare Advantage plans, cost plans,
and Health Care Prepayment Plans
(HCPPs), are required to issue the Notice
of Denial of Medical Coverage (or
Payment) (NDMCP) when a request for
either a medical service or payment is
denied, in whole or in part.
Additionally, the notices inform
Medicare enrollees of their right to file
an appeal, outlining the steps and
timeframes for filing. All Medicare
health plans are required to use these
standardized notices. Form Number:
CMS–10003 (OMB Control Number:
0938–0829); Frequency: Annually;
Affected Public: Private Sector, Business
or other for-profit and not-for-profit
institutions; Number of Respondents:
937; Number of Responses: 16,191,812;
Total Annual Hours: 2,697,556. (For
policy questions regarding this
collection contact Sabrina Edmonston at
410–786–3209.)
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title: Emergency
and Foreign Hospital Services and
Supporting Regulation in 42 CFR
Section 424.103; Use: Section 1866 of
the Social Security Act states that any
provider of services shall be qualified to
participate in the Medicare program and
shall be eligible for payments under
Medicare if it files an agreement with
the Secretary to meet the conditions
outlined in this section of the Act.
Section 1814(d)(1) of the Social Security
Act and 42 CFR 424.100, allows
payment of Medicare benefits for a
Medicare beneficiary to a
nonparticipating hospital that does not
have an agreement in effect with the
Centers for Medicare and Medicaid
Services. These payments can be made
if such services were emergency
services and if CMS would be required
to make the payment if the hospital had
an agreement in effect and met the
conditions of payment. This form is
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used in connection with claims for
emergency hospital services provided
by hospitals that do not have an
agreement in effect under Section 1866
of the Social Security Act.
42 CFR 424.103(b) requires that before
a non-participating hospital may be paid
for emergency services rendered to a
Medicare beneficiary, a statement must
be submitted that is sufficiently
comprehensive to support that an
emergency existed. Form CMS–1771
contains a series of questions relating to
the medical necessity of the emergency.
The attending physician must attest that
the hospitalization was required under
the regulatory emergency definition (42
CFR 424.101 attached) and give clinical
documentation to support the claim. A
photocopy of the beneficiary’s hospital
records may be used in lieu of the CMS–
1771 if the records contain all the
information required by the form; Form
Number: CMS–1771 (OMB Control
Number: 0938–0023); Frequency:
Annually; Affected Public: Private
Sector, Business or other for-profit and
not-for-profit institutions; Number of
Respondents: 100; Number of
Responses: 200; Total Annual Hours:
50. (For policy questions regarding this
collection contact Shauntari Cheely at
410–786–1818.)
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title: Programs of
All-Inclusive Care for the Elderly
(PACE); Use: PACE is a pre-paid,
capitated plan that provides
comprehensive health care services to
frail, older adults in the community,
who are eligible for nursing home care
according to state standards. PACE
programs must provide all Medicare and
Medicaid covered services; financing of
this model is accomplished through
prospective capitation of both Medicare
and Medicaid payments. Upon approval
of a PACE application, CMS executes a
three-way program agreement with the
applicant entity and the applicable
state. With certain exceptions, this
information collection addresses all
operational components of the PACE
program, as defined in 42 CFR part 460.
Form Number: CMS–R–244 (OMB
control number: 0938–0790); Frequency:
Once and occasionally; Affected Public:
Private sector (Business or other for
profits and Not-for-profit institutions);
Number of Respondents: 179; Total
Annual Responses: 121,407; Total
Annual Hours: 97,069. (For policy
questions regarding this collection
contact Lauren Brandow at 410–786–
9765.)
4. Type of Information Collection
Request: Revision of a currently
approved collection; Title: Medicare
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Durable Medical Equipment,
Prosthetics, Orthotics, and Supplies
(DMEPOS) Competitive Bidding
Program—Contracting Forms; Use:
Since 1989, Medicare has been paying
for durable medical equipment,
prosthetics, orthotics, and supplies
(DMEPOS) (other than customized
items) using fee schedule amounts that
are calculated for each item or category
of DMEPOS identified by a Healthcare
Common Procedure Coding System
(HCPCS) code. Payments are based on
the average DMEPOS supplier charges
on Medicare claims from 1986 and 1987
and are updated annually on a factor
legislated by Congress. For many years,
the Government Accountability Office
(GAO) and the Office of Inspector
General (OIG) of the United States (U.S.)
Department of Health and Human
Services (HHS) have reported that these
fees are often highly inflated and that
Medicare has paid higher than market
rates for several different types of
DMEPOS. Due to reports of Medicare
overpayment of DMEPOS, Congress
required that the Centers for Medicare &
Medicaid Services (CMS) conduct a
competitive bidding demonstration
project for these items. Accordingly,
CMS implemented a demonstration
project for this program from 1999–2002
which produced significant savings for
beneficiaries and taxpayers without
hindering access to DMEPOS and
related services. Shortly after the
successful competitive bidding
demonstrations, Congress passed the
Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA) and mandated a phased-in
approach to implement this program
over the course of several years
beginning in 2007 in 10 metropolitan
statistical areas (MSAs). This statute
specifically required the Secretary to
establish and implement programs
under which competitive bidding areas
(CBAs) are established throughout the
U.S. for contract award purposes for the
furnishing of certain competitively
priced items and services for which
payment is made under Medicare Part
B. This program is commonly known as
the Medicare DMEPOS Competitive
Bidding Program (the Program).
CMS conducted its first round of
bidding, Round 1, for the Program in
2007 with the help of its contractor, the
Competitive Bidding Implementation
Contractor (CBIC). CMS published a
Request for Bids (RFB) and instructions
for DMEPOS suppliers to submit their
bids to participate in the Program.
During this first round of bidding,
DMEPOS suppliers from across the U.S.
submitted bids to furnish competitively
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bid item(s) to Medicare beneficiaries
residing or traveling to Round 1 CBAs.
CMS evaluated these bids and
contracted with those bidders that met
all program requirements. Round 1 was
successfully implemented on July 1,
2008.
On July 15, 2008, however, Congress
delayed the Program in section 154 of
the Medicare Improvements for Patients
and Providers Act of 2008 (MIPPA).
MIPPA mandated certain changes to the
Program which included, but was not
limited to: a delay of Round 1
(competition to begin in 2009) and
Round 2 of the Program (competition to
begin in 2011 in 70 specific MSAs); the
exclusion of Puerto Rico and negative
pressure wound therapy from Round 1
and Group 3 complex rehabilitative
power wheelchairs from all rounds of
competition; a process for providing
feedback to bidders regarding missing
financial documentation; and a
requirement for contract suppliers to
disclose to CMS information regarding
subcontracting relationships. Section
154 of MIPPA specified that the
competition for national mail-order
(NMO) items and services may be
phased in after 2010. This section of
MIPPA also specified that competitions
to phase-in additional areas could occur
after 2011. As required by MIPPA, CMS
conducted the competition for the
Round 1 Rebid in 2009. The Round 1
Rebid contracts and prices became
effective on January 1, 2011. The
Affordable Care Act (ACA), enacted on
March 23, 2010, expanded the Round 2
competition by adding an additional 21
MSAs, bringing the total MSAs for
Round 2 to 91. The competition for
Round 2 began in December 2011. CMS
also began a NMO competition for
diabetes testing supplies (DTS) at the
same time as Round 2. The Round 2 and
NMO DTS contracts and prices were
implemented on July 1, 2013.
The MMA requires the Secretary to
recompete contracts not less often than
once every three years. The Round 1
Rebid contract period for all product
categories except NMO DTS expired on
December 31, 2013. (Round 1 Rebid
contracts for NMO DTS ended on
December 31, 2012.) The competition
for the Round 1 Recompete began in
August of 2012 and contracts and prices
became effective on January 1, 2014.
The Round 1 Recompete contract period
expired on December 31, 2016. Round 1
2017 contracts were effective on January
1, 2017, and expired on December 31,
2018. Round 2 and NMO DTS contracts
and prices expired on June 30, 2016.
Round 2 Recompete and the NMO DTS
Recompete contracts became effective
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on July 1, 2016, and expired on
December 31, 2018.
On October 31, 2018, CMS issued a
final rule (CMS–1691–F) requiring
changes to bidding and pricing
methodologies to be implemented under
the next round of the Program. As a
result, starting January 1, 2019, there
was a temporary gap in the entire
Program that lasted two years until
December 31, 2020. When the program
resumed in January 2021, CMS
implemented a consolidated round of
competition to include most Round 1
2017 and Round 2 Recompete CBAs for
Round 2021. However, due to the 2019
novel coronavirus (COVID–19)
pandemic, and the unexpected bid
evaluation results, CMS only awarded
Round 2021 contracts for two product
categories: Off-The-Shelf (OTS) Back
and OTS Knee Braces. As a result, this
Paperwork Reduction Act (PRA)
package reflects a significant reduction
in burden, compared to previous
packages, for Round 2021 which was
implemented on January 1, 2021, and
will concluded on December 31, 2023.
This iteration of the package currently
approved under OMB control number
0938–1408 is based on data from the
first year of Round 2021 (January 1,
2021–December 31, 2021). Form
Number: CMS–10744 (OMB control
number: 0938–1408); Frequency:
Occasionally; Affected Public: Private
sector (Business or other for profits and
Not-for-profit institutions); Number of
Respondents: 179; Total Annual
Responses: 121,407; Total Annual
Hours: 97,069. (For policy questions
regarding this collection contact Julia
Howard at 410–786–845.)
Dated: August 2, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–16869 Filed 8–4–22; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10553, CMS–
R–305 and CMS–10492]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
PO 00000
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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 September 6, 2022.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
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/Regulationsand-Guidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing
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
DATES:
E:\FR\FM\05AUN1.SGM
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Agencies
[Federal Register Volume 87, Number 150 (Friday, August 5, 2022)]
[Notices]
[Pages 48030-48032]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-16869]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers: CMS-10003, CMS-1771, CMS-R-244 and CMS-10744]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
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 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 October 4, 2022.
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 website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.
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-10003--Notice of Denial of Medical Coverage (or Payment)
CMS-1771--Emergency and Foreign Hospital Services and Supporting
Regulation in 42 CFR Section 424.103
CMS-R-244--Programs of All-Inclusive Care for the Elderly (PACE)
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
[[Page 48031]]
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 of a currently
approved collection; Title: Notice of Denial of Medical Coverage (or
Payment); Use: Section 1852(g)(1)(B) of the Social Security Act (the
Act) requires Medicare health plans to provide enrollees with a written
notice in understandable language of the reasons for the denial and a
description of the applicable appeals processes.
Medicare health plans, including Medicare Advantage plans, cost
plans, and Health Care Prepayment Plans (HCPPs), are required to issue
the Notice of Denial of Medical Coverage (or Payment) (NDMCP) when a
request for either a medical service or payment is denied, in whole or
in part. Additionally, the notices inform Medicare enrollees of their
right to file an appeal, outlining the steps and timeframes for filing.
All Medicare health plans are required to use these standardized
notices. Form Number: CMS-10003 (OMB Control Number: 0938-0829);
Frequency: Annually; Affected Public: Private Sector, Business or other
for-profit and not-for-profit institutions; Number of Respondents: 937;
Number of Responses: 16,191,812; Total Annual Hours: 2,697,556. (For
policy questions regarding this collection contact Sabrina Edmonston at
410-786-3209.)
2. Type of Information Collection Request: Extension of a currently
approved collection; Title: Emergency and Foreign Hospital Services and
Supporting Regulation in 42 CFR Section 424.103; Use: Section 1866 of
the Social Security Act states that any provider of services shall be
qualified to participate in the Medicare program and shall be eligible
for payments under Medicare if it files an agreement with the Secretary
to meet the conditions outlined in this section of the Act. Section
1814(d)(1) of the Social Security Act and 42 CFR 424.100, allows
payment of Medicare benefits for a Medicare beneficiary to a
nonparticipating hospital that does not have an agreement in effect
with the Centers for Medicare and Medicaid Services. These payments can
be made if such services were emergency services and if CMS would be
required to make the payment if the hospital had an agreement in effect
and met the conditions of payment. This form is used in connection with
claims for emergency hospital services provided by hospitals that do
not have an agreement in effect under Section 1866 of the Social
Security Act.
42 CFR 424.103(b) requires that before a non-participating hospital
may be paid for emergency services rendered to a Medicare beneficiary,
a statement must be submitted that is sufficiently comprehensive to
support that an emergency existed. Form CMS-1771 contains a series of
questions relating to the medical necessity of the emergency. The
attending physician must attest that the hospitalization was required
under the regulatory emergency definition (42 CFR 424.101 attached) and
give clinical documentation to support the claim. A photocopy of the
beneficiary's hospital records may be used in lieu of the CMS-1771 if
the records contain all the information required by the form; Form
Number: CMS-1771 (OMB Control Number: 0938-0023); Frequency: Annually;
Affected Public: Private Sector, Business or other for-profit and not-
for-profit institutions; Number of Respondents: 100; Number of
Responses: 200; Total Annual Hours: 50. (For policy questions regarding
this collection contact Shauntari Cheely at 410-786-1818.)
3. Type of Information Collection Request: Revision of a currently
approved collection; Title: Programs of All-Inclusive Care for the
Elderly (PACE); Use: PACE is a pre-paid, capitated plan that provides
comprehensive health care services to frail, older adults in the
community, who are eligible for nursing home care according to state
standards. PACE programs must provide all Medicare and Medicaid covered
services; financing of this model is accomplished through prospective
capitation of both Medicare and Medicaid payments. Upon approval of a
PACE application, CMS executes a three-way program agreement with the
applicant entity and the applicable state. With certain exceptions,
this information collection addresses all operational components of the
PACE program, as defined in 42 CFR part 460. Form Number: CMS-R-244
(OMB control number: 0938-0790); Frequency: Once and occasionally;
Affected Public: Private sector (Business or other for profits and Not-
for-profit institutions); Number of Respondents: 179; Total Annual
Responses: 121,407; Total Annual Hours: 97,069. (For policy questions
regarding this collection contact Lauren Brandow at 410-786-9765.)
4. Type of Information Collection Request: Revision of a currently
approved collection; Title: Medicare Durable Medical Equipment,
Prosthetics, Orthotics, and Supplies (DMEPOS) Competitive Bidding
Program--Contracting Forms; Use: Since 1989, Medicare has been paying
for durable medical equipment, prosthetics, orthotics, and supplies
(DMEPOS) (other than customized items) using fee schedule amounts that
are calculated for each item or category of DMEPOS identified by a
Healthcare Common Procedure Coding System (HCPCS) code. Payments are
based on the average DMEPOS supplier charges on Medicare claims from
1986 and 1987 and are updated annually on a factor legislated by
Congress. For many years, the Government Accountability Office (GAO)
and the Office of Inspector General (OIG) of the United States (U.S.)
Department of Health and Human Services (HHS) have reported that these
fees are often highly inflated and that Medicare has paid higher than
market rates for several different types of DMEPOS. Due to reports of
Medicare overpayment of DMEPOS, Congress required that the Centers for
Medicare & Medicaid Services (CMS) conduct a competitive bidding
demonstration project for these items. Accordingly, CMS implemented a
demonstration project for this program from 1999-2002 which produced
significant savings for beneficiaries and taxpayers without hindering
access to DMEPOS and related services. Shortly after the successful
competitive bidding demonstrations, Congress passed the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) and
mandated a phased-in approach to implement this program over the course
of several years beginning in 2007 in 10 metropolitan statistical areas
(MSAs). This statute specifically required the Secretary to establish
and implement programs under which competitive bidding areas (CBAs) are
established throughout the U.S. for contract award purposes for the
furnishing of certain competitively priced items and services for which
payment is made under Medicare Part B. This program is commonly known
as the Medicare DMEPOS Competitive Bidding Program (the Program).
CMS conducted its first round of bidding, Round 1, for the Program
in 2007 with the help of its contractor, the Competitive Bidding
Implementation Contractor (CBIC). CMS published a Request for Bids
(RFB) and instructions for DMEPOS suppliers to submit their bids to
participate in the Program. During this first round of bidding, DMEPOS
suppliers from across the U.S. submitted bids to furnish competitively
[[Page 48032]]
bid item(s) to Medicare beneficiaries residing or traveling to Round 1
CBAs. CMS evaluated these bids and contracted with those bidders that
met all program requirements. Round 1 was successfully implemented on
July 1, 2008.
On July 15, 2008, however, Congress delayed the Program in section
154 of the Medicare Improvements for Patients and Providers Act of 2008
(MIPPA). MIPPA mandated certain changes to the Program which included,
but was not limited to: a delay of Round 1 (competition to begin in
2009) and Round 2 of the Program (competition to begin in 2011 in 70
specific MSAs); the exclusion of Puerto Rico and negative pressure
wound therapy from Round 1 and Group 3 complex rehabilitative power
wheelchairs from all rounds of competition; a process for providing
feedback to bidders regarding missing financial documentation; and a
requirement for contract suppliers to disclose to CMS information
regarding subcontracting relationships. Section 154 of MIPPA specified
that the competition for national mail-order (NMO) items and services
may be phased in after 2010. This section of MIPPA also specified that
competitions to phase-in additional areas could occur after 2011. As
required by MIPPA, CMS conducted the competition for the Round 1 Rebid
in 2009. The Round 1 Rebid contracts and prices became effective on
January 1, 2011. The Affordable Care Act (ACA), enacted on March 23,
2010, expanded the Round 2 competition by adding an additional 21 MSAs,
bringing the total MSAs for Round 2 to 91. The competition for Round 2
began in December 2011. CMS also began a NMO competition for diabetes
testing supplies (DTS) at the same time as Round 2. The Round 2 and NMO
DTS contracts and prices were implemented on July 1, 2013.
The MMA requires the Secretary to recompete contracts not less
often than once every three years. The Round 1 Rebid contract period
for all product categories except NMO DTS expired on December 31, 2013.
(Round 1 Rebid contracts for NMO DTS ended on December 31, 2012.) The
competition for the Round 1 Recompete began in August of 2012 and
contracts and prices became effective on January 1, 2014. The Round 1
Recompete contract period expired on December 31, 2016. Round 1 2017
contracts were effective on January 1, 2017, and expired on December
31, 2018. Round 2 and NMO DTS contracts and prices expired on June 30,
2016. Round 2 Recompete and the NMO DTS Recompete contracts became
effective on July 1, 2016, and expired on December 31, 2018.
On October 31, 2018, CMS issued a final rule (CMS-1691-F) requiring
changes to bidding and pricing methodologies to be implemented under
the next round of the Program. As a result, starting January 1, 2019,
there was a temporary gap in the entire Program that lasted two years
until December 31, 2020. When the program resumed in January 2021, CMS
implemented a consolidated round of competition to include most Round 1
2017 and Round 2 Recompete CBAs for Round 2021. However, due to the
2019 novel coronavirus (COVID-19) pandemic, and the unexpected bid
evaluation results, CMS only awarded Round 2021 contracts for two
product categories: Off-The-Shelf (OTS) Back and OTS Knee Braces. As a
result, this Paperwork Reduction Act (PRA) package reflects a
significant reduction in burden, compared to previous packages, for
Round 2021 which was implemented on January 1, 2021, and will concluded
on December 31, 2023. This iteration of the package currently approved
under OMB control number 0938-1408 is based on data from the first year
of Round 2021 (January 1, 2021-December 31, 2021). Form Number: CMS-
10744 (OMB control number: 0938-1408); Frequency: Occasionally;
Affected Public: Private sector (Business or other for profits and Not-
for-profit institutions); Number of Respondents: 179; Total Annual
Responses: 121,407; Total Annual Hours: 97,069. (For policy questions
regarding this collection contact Julia Howard at 410-786-845.)
Dated: August 2, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2022-16869 Filed 8-4-22; 8:45 am]
BILLING CODE 4120-01-P