Agency Information Collection Activities: Proposed Collection; Comment Request, 13878-13880 [2013-04752]
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13878
Federal Register / Vol. 78, No. 41 / Friday, March 1, 2013 / Notices
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than March 28,
2013.
A. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. Eagle Bancshares, Inc., Eagle,
Nebraska; to become a bank holding
company by acquiring 100 percent of
the voting shares of Eagle State Bank,
Eagle, Nebraska.
Board of Governors of the Federal Reserve
System, February 25, 2013.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
[FR Doc. 2013–04765 Filed 2–28–13; 8:45 am]
(BHC Act), Regulation Y (12 CFR part
225), and all other applicable statutes
and regulations to become a bank
holding company and/or to acquire the
assets or the ownership of, control of, or
the power to vote shares of a bank or
bank holding company and all of the
banks and nonbanking companies
owned by the bank holding company,
including the companies listed below.
The applications listed below, as well
as other related filings required by the
Board, are available for immediate
inspection at the Federal Reserve Bank
indicated. The applications will also be
available for inspection at the offices of
the Board of Governors. Interested
persons may express their views in
writing on the standards enumerated in
the BHC Act (12 U.S.C. 1842(c)). If the
proposal also involves the acquisition of
a nonbanking company, the review also
includes whether the acquisition of the
nonbanking company complies with the
standards in section 4 of the BHC Act
(12 U.S.C. 1843). Unless otherwise
noted, nonbanking activities will be
conducted throughout the United States.
Unless otherwise noted, comments
regarding each of these applications
must be received at the Reserve Bank
indicated or the offices of the Board of
Governors not later than March 25,
2013.
A. Federal Reserve Bank of Kansas
City (Dennis Denney, Assistant Vice
President) 1 Memorial Drive, Kansas
City, Missouri 64198–0001:
1. BancFirst Corporation, Oklahoma
City, Oklahoma; to acquire control of
Spirit Bankcorp, Inc., Bristow,
Oklahoma, and thereby indirectly
acquire voting shares of SpiritBank,
Tulsa, Oklahoma.
Board of Governors of the Federal Reserve
System, February 25, 2013.
Margaret McCloskey Shanks,
Deputy Secretary of the Board.
[FR Doc. 2013–04766 Filed 2–28–13; 8:45 am]
BILLING CODE 6210–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
BILLING CODE 6210–01–P
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[Document Identifiers CMS–588 and CMS–
10169]
FEDERAL RESERVE SYSTEM
Formations of, Acquisitions by, and
Mergers of Bank Holding Companies
The companies listed in this notice
have applied to the Board for approval,
pursuant to the Bank Holding Company
Act of 1956 (12 U.S.C. 1841 et seq.)
VerDate Mar<15>2010
16:40 Feb 28, 2013
Jkt 229001
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
AGENCY:
PO 00000
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Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
estimate or any other aspect of this
collection of information, including any
of the following subjects: (1) The
necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions;
(2) the accuracy of the estimated
burden; (3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and (4) the use of
automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
1. Type of Information Collection
Request: Revision of a currently
approved collection. Title of
Information Collection: Electronic
Funds Transfers Authorization
Agreement Use: The primary function of
the Electronic Funds Transfer
Authorization Agreement (CMS 588) is
to gather information from a provider/
supplier to establish an electronic
payment process.
The legal authority to collect this
information is found in Section 1815(a)
of the Social Security Act. This section
provides authority for the Secretary of
Health and Human Services to pay
providers/suppliers of Medicare
services. Under 31 U.S.C. 3332(f)(1), all
federal payments, including Medicare
payments to providers and suppliers,
shall be made by electronic funds
transfer. 31 U.S.C. 7701 (c) requires that
any person or entity doing business
with the federal government must
provide their Tax Identification Number
(TIN).
The goal of this submission is to
renew the data collection. Only two
minor revisions for systems
requirements will be made at this time,
specifically adding a street address line
for the location of the financial
institution and adding an additional
National Provider Identification (NPI)
number collection field for those
providers/suppliers who have more
than one NPI. Form Number: CMS–588
(OCN: 0938–0626). Frequency:
Occasionally. Affected Public: Private
Sector (business or other for-profits) and
Not-for-profit institutions. Number of
Respondents: 94,000. Total Annual
Responses: 94,000. Total Annual Hours:
23,500. (For policy questions regarding
this collection contact Kim McPhillips
at 410–786–5374. For all other issues
call 410–786–1326.)
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Federal Register / Vol. 78, No. 41 / Friday, March 1, 2013 / Notices
2. Type of Information Collection
Request: Revision of a currently
approved collection. Title of
Information Collection: Medicare
Durable Medical Equipment,
Prosthetics, Orthotics and Supplies
(DMEPOS) Competitive Bidding
Program. Use: Since 1989, Medicare has
been paying for durable medical
equipment (DME) and supplies (other
than customized items) using fee
schedule amounts that are calculated for
each item or category of DME identified
by a Healthcare Common Procedure
Coding System code. Payments are
based on the average 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
and the Office of Inspector General of
the U.S. Department of Health and
Human Services have reported that
these fees are often highly inflated and
that Medicare has paid higher than
market rates for several different types
of DME. Due to reports of Medicare
overpayment of DME and supplies,
Congress required that 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 a
successful demonstration of the
competitive bidding program, Congress
passed the Medicare Prescription Drug,
Improvement and Modernization Act of
2003 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). The statute
specifically required the Secretary to
establish and implement programs
under which competitive bidding areas
are established throughout the United
States 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.’’
CMS conducted its first round of
bidding for the Medicare DMEPOS
Competitive Bidding Program in 2007
with the help of its contractor, the
Competitive Bidding Implementation
Contractor. CMS published a Request
for Bids instructions and accompanying
forms for suppliers to submit their bids
to participate in the program. During
this first round of bidding, DMEPOS
suppliers from across the U.S. submitted
VerDate Mar<15>2010
16:40 Feb 28, 2013
Jkt 229001
bids identifying the MSA(s) to service
and the competitively bid item(s) they
wished to furnish to Medicare
beneficiaries. CMS evaluated these bids
and contracted with those suppliers that
met all program requirements. The first
round of bidding was successfully
implemented on July 1, 2008.
On July 15, 2008, however, Congress
delayed this program in section 154 of
the Medicare Improvements for Patients
and Providers Act of 2008 (MIPPA).
MIPPA mandated certain changes to the
competitive bidding program which
included, but are not limited to: A delay
of Rounds 1 (competition began in 2009)
and 2 of the program (competition began
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 suppliers regarding missing
financial documentation; and a
requirement for contract suppliers to
disclose to CMS information regarding
subcontracting relationships. Section
154 of the MIPPA specified that the
competition for national mail order
items and services may be phased in
after 2010 and established a rule
requiring that a bidder demonstrate that
its bid covers 50 percent (or higher) of
the types of diabetic testing strips, based
on volume (the ‘‘50 percent rule’’) for
national mail order competitions. 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, 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 competition for National
Mail Order of Diabetic Testing Supplies
at the same time as Round 2. The Round
2 and National Mail-Order contracts and
prices have a target implementation date
of July 1, 2013.
The MMA requires the Secretary to recompete contracts not less often than
once every 3 years. Most Round 1 Rebid
contracts will expire on December 31,
2013. (Round 1 Rebid contracts for mailorder diabetic testing supplies ended on
December 31, 2012.) Consequently, we
are currently in the process of recompeting the competitive bidding
contracts in the Round 1 Rebid areas.
The most recent approval for this
information collection request (ICR) was
issued by OMB on October 10, 2012.
Since then, CMS has decided to
sequentially update the paperwork
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13879
burden necessary to administer the
program as it expands nationally and
cycles through multiple rounds of
competition. Specifically, we are now
seeking to update our burden estimates
for certain contract maintenance forms
for Round 2 and the national mail-order
competitions. These include Form C
and the Contract Supplier’s Disclosure
of Subcontractors form. We are also
requesting approval of two additional
forms: The Change of Ownership
(CHOW) Purchaser Form and the CHOW
Contract Supplier Notification Form,
which will be utilized in all rounds of
competition. Finally, we are retaining
without change Forms A, B, and D and
their associated burden under this ICR.
We note that the information collection
for Forms A and B is already complete.
We intend to continue use of the Forms
in future rounds of competition. Form
Number: CMS–10169 (OCN: 0938–
1016). Frequency: Occasionally.
Affected Public: Private Sector (business
or other for-profits) and Individuals or
households. Number of Respondents:
19,035. Total Annual Responses:
19,035. Total Annual Hours: 9,311. (For
policy questions regarding this
collection contact Michael Keane at
410–786–4495. For all other issues call
410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or
Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by April 30, 2013:
1. Electronically. You may submit
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) 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.
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Federal Register / Vol. 78, No. 41 / Friday, March 1, 2013 / Notices
or passport) and to state the purpose of their
visit.
Dated: February 26, 2013.
Martique Jones,
Deputy Director, Regulations Development
Group, Office of Strategic Operations and
Regulatory Affairs.
Dated: February 25, 2013.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–04752 Filed 2–28–13; 8:45 am]
BILLING CODE 4120–01–P
[FR Doc. 2013–04740 Filed 2–28–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Clinical Center; Notice of Meeting
National Institutes of Health
mstockstill on DSK4VPTVN1PROD with NOTICES
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of a meeting of the NIH
Advisory Board for Clinical Research.
The meeting will be open to the
public as indicated below, with
attendance limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the Contact Person listed below
in advance of the meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in section
552b(c)(6), Title 5 U.S.C., as amended to
discuss personnel matters, the
disclosure of which would constitute a
clearly unwarranted invasion of privacy.
Name of Committee: NIH Advisory Board
for Clinical Research.
Date: March 18, 2013.
Open: 10:00 a.m. to 1:15 p.m.
Agenda: To review the FY14 Clinical
Center Budget.
Place: National Institutes of Health,
Building 10, 10 Center Drive, CRC Medical
Board Room 4–2551, Bethesda, MD 20892.
Closed: 1:15 p.m. to 2:00 p.m.
Agenda: To discuss personnel matters and/
or issues of which the premature disclosure
may affect outcomes.
Place: National Institutes of Health,
Building 10, 10 Center Drive, CRC Medical
Board Room 4–2551, Bethesda, MD 20892.
Contact Person: Maureen E Gormley,
Executive Secretary, Mark O. Hatfield
Clinical Research Center, National Institutes
of Health, Building 10, Room 6–2551,
Bethesda, MD 20892, (301) 496–2897.
Any interested person may file written
comments with the committee by forwarding
the statement to the Contact Person listed on
this notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
In the interest of security, NIH has
instituted stringent procedures for entrance
onto the NIH campus. All visitor vehicles,
including taxicabs, hotel, and airport shuttles
will be inspected before being allowed on
campus. Visitors will be asked to show one
form of identification (for example, a
government-issued photo ID, driver’s license,
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16:40 Feb 28, 2013
Jkt 229001
National Heart, Lung, and Blood
Institute; Notice of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Heart, Lung, and
Blood Initial Review Group, Heart, Lung, and
Blood Program Project Review Committee.
Date: March 22, 2013.
Time: 8:00 a.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Doubletree Hotel Bethesda,
(Formerly Holiday Inn Select), 8120
Wisconsin Avenue, Bethesda, MD 20814.
Contact Person: Jeffrey H Hurst, Ph.D.,
Scientific Review Officer, Office of Scientific
Review/DERA, National Heart, Lung, and
Blood Institute, National Institutes of Health,
6701 Rockledge Drive, Room 7208, Bethesda,
MD 20892, 301–435–0303,
hurstj@nhlbi.nih.gov.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.233, National Center for
Sleep Disorders Research; 93.837, Heart and
Vascular Diseases Research; 93.838, Lung
Diseases Research; 93.839, Blood Diseases
and Resources Research, National Institutes
of Health, HHS)
Dated: February 25, 2013.
Michelle Trout,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–04739 Filed 2–28–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: Center for Scientific
Review Special Emphasis Panel, Systems
Biology and Networks Specials.
Date: March 12, 2013.
Time: 3:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health, 6701
Rockledge Drive, Bethesda, MD 20892
(Telephone Conference Call).
Contact Person: Barbara J Thomas, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 2218,
MSC 7890, Bethesda, MD 20892, 301–435–
0603, bthomas@csr.nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.306, Comparative Medicine;
93.333, Clinical Research, 93.306, 93.333,
93.337, 93.393–93.396, 93.837–93.844,
93.846–93.878, 93.892, 93.893, National
Institutes of Health, HHS)
Dated: February 25, 2013.
Melanie J. Gray,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2013–04736 Filed 2–28–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meetings.
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Agencies
[Federal Register Volume 78, Number 41 (Friday, March 1, 2013)]
[Notices]
[Pages 13878-13880]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-04752]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifiers CMS-588 and CMS-10169]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS) is publishing the following summary of proposed
collections for public comment. Interested persons are invited to send
comments regarding this burden estimate or any other aspect of this
collection of information, including any of the following subjects: (1)
The necessity and utility of the proposed information collection for
the proper performance of the agency's functions; (2) the accuracy of
the estimated burden; (3) ways to enhance the quality, utility, and
clarity of the information to be collected; and (4) the use of
automated collection techniques or other forms of information
technology to minimize the information collection burden.
1. Type of Information Collection Request: Revision of a currently
approved collection. Title of Information Collection: Electronic Funds
Transfers Authorization Agreement Use: The primary function of the
Electronic Funds Transfer Authorization Agreement (CMS 588) is to
gather information from a provider/supplier to establish an electronic
payment process.
The legal authority to collect this information is found in Section
1815(a) of the Social Security Act. This section provides authority for
the Secretary of Health and Human Services to pay providers/suppliers
of Medicare services. Under 31 U.S.C. 3332(f)(1), all federal payments,
including Medicare payments to providers and suppliers, shall be made
by electronic funds transfer. 31 U.S.C. 7701 (c) requires that any
person or entity doing business with the federal government must
provide their Tax Identification Number (TIN).
The goal of this submission is to renew the data collection. Only
two minor revisions for systems requirements will be made at this time,
specifically adding a street address line for the location of the
financial institution and adding an additional National Provider
Identification (NPI) number collection field for those providers/
suppliers who have more than one NPI. Form Number: CMS-588 (OCN: 0938-
0626). Frequency: Occasionally. Affected Public: Private Sector
(business or other for-profits) and Not-for-profit institutions. Number
of Respondents: 94,000. Total Annual Responses: 94,000. Total Annual
Hours: 23,500. (For policy questions regarding this collection contact
Kim McPhillips at 410-786-5374. For all other issues call 410-786-
1326.)
[[Page 13879]]
2. Type of Information Collection Request: Revision of a currently
approved collection. Title of Information Collection: Medicare Durable
Medical Equipment, Prosthetics, Orthotics and Supplies (DMEPOS)
Competitive Bidding Program. Use: Since 1989, Medicare has been paying
for durable medical equipment (DME) and supplies (other than customized
items) using fee schedule amounts that are calculated for each item or
category of DME identified by a Healthcare Common Procedure Coding
System code. Payments are based on the average 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 and the Office of Inspector General of the U.S. Department of
Health and Human Services have reported that these fees are often
highly inflated and that Medicare has paid higher than market rates for
several different types of DME. Due to reports of Medicare overpayment
of DME and supplies, Congress required that 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
a successful demonstration of the competitive bidding program, Congress
passed the Medicare Prescription Drug, Improvement and Modernization
Act of 2003 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). The statute specifically required the
Secretary to establish and implement programs under which competitive
bidding areas are established throughout the United States 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.''
CMS conducted its first round of bidding for the Medicare DMEPOS
Competitive Bidding Program in 2007 with the help of its contractor,
the Competitive Bidding Implementation Contractor. CMS published a
Request for Bids instructions and accompanying forms for 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
identifying the MSA(s) to service and the competitively bid item(s)
they wished to furnish to Medicare beneficiaries. CMS evaluated these
bids and contracted with those suppliers that met all program
requirements. The first round of bidding was successfully implemented
on July 1, 2008.
On July 15, 2008, however, Congress delayed this program in section
154 of the Medicare Improvements for Patients and Providers Act of 2008
(MIPPA). MIPPA mandated certain changes to the competitive bidding
program which included, but are not limited to: A delay of Rounds 1
(competition began in 2009) and 2 of the program (competition began 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 suppliers regarding missing financial
documentation; and a requirement for contract suppliers to disclose to
CMS information regarding subcontracting relationships. Section 154 of
the MIPPA specified that the competition for national mail order items
and services may be phased in after 2010 and established a rule
requiring that a bidder demonstrate that its bid covers 50 percent (or
higher) of the types of diabetic testing strips, based on volume (the
``50 percent rule'') for national mail order competitions. 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, 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 competition for National Mail Order of Diabetic
Testing Supplies at the same time as Round 2. The Round 2 and National
Mail-Order contracts and prices have a target implementation date of
July 1, 2013.
The MMA requires the Secretary to re-compete contracts not less
often than once every 3 years. Most Round 1 Rebid contracts will expire
on December 31, 2013. (Round 1 Rebid contracts for mail-order diabetic
testing supplies ended on December 31, 2012.) Consequently, we are
currently in the process of re-competing the competitive bidding
contracts in the Round 1 Rebid areas.
The most recent approval for this information collection request
(ICR) was issued by OMB on October 10, 2012. Since then, CMS has
decided to sequentially update the paperwork burden necessary to
administer the program as it expands nationally and cycles through
multiple rounds of competition. Specifically, we are now seeking to
update our burden estimates for certain contract maintenance forms for
Round 2 and the national mail-order competitions. These include Form C
and the Contract Supplier's Disclosure of Subcontractors form. We are
also requesting approval of two additional forms: The Change of
Ownership (CHOW) Purchaser Form and the CHOW Contract Supplier
Notification Form, which will be utilized in all rounds of competition.
Finally, we are retaining without change Forms A, B, and D and their
associated burden under this ICR. We note that the information
collection for Forms A and B is already complete. We intend to continue
use of the Forms in future rounds of competition. Form Number: CMS-
10169 (OCN: 0938-1016). Frequency: Occasionally. Affected Public:
Private Sector (business or other for-profits) and Individuals or
households. Number of Respondents: 19,035. Total Annual Responses:
19,035. Total Annual Hours: 9,311. (For policy questions regarding this
collection contact Michael Keane at 410-786-4495. For all other issues
call 410-786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web site address at https://www.cms.hhs.gov/PaperworkReductionActof1995,
or Email your request, including your address, phone number, OMB
number, and CMS document identifier, to Paperwork@cms.hhs.gov, or call
the Reports Clearance Office on (410) 786-1326.
In commenting on the proposed information collections please
reference the document identifier or OMB control number. To be assured
consideration, comments and recommendations must be submitted in one of
the following ways by April 30, 2013:
1. Electronically. You may submit 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) 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.
[[Page 13880]]
Dated: February 26, 2013.
Martique Jones,
Deputy Director, Regulations Development Group, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2013-04752 Filed 2-28-13; 8:45 am]
BILLING CODE 4120-01-P