Agency Information Collection Activities: Proposed Collection; Comment Request, 39812-39813 [E7-13904]
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Federal Register / Vol. 72, No. 139 / Friday, July 20, 2007 / Notices
Reserve Bank indicated. The notices
also will be available for inspection at
the office of the Board of Governors.
Interested persons may express their
views in writing to the Reserve Bank
indicated for that notice or to the offices
of the Board of Governors. Comments
must be received not later than August
6, 2007.
A. Federal Reserve Bank of Chicago
(Burl Thornton, Assistant Vice
President) 230 South LaSalle Street,
Chicago, Illinois 60690-1414:
1. David A. Davis, Muskego,
Wisconsin; to acquire voting shares of
Capital Commerce Bancorp, Inc., and
thereby indirectly acquire voting shares
of MW Bank, both of Milwaukee,
Wisconsin.
Board of Governors of the Federal Reserve
System, July 17, 2007.
Robert deV. Frierson,
Deputy Secretary of the Board.
[FR Doc. E7–14066 Filed 7–19–07; 8:45 am]
BILLING CODE 6210–01–S
GENERAL SERVICES
ADMINISTRATION
Request for Comments on Proposed
Federal Emergency Travel Guide
Office of Governmentwide
Policy, General Services Administration
(GSA).
ACTION: Notice of intent and request for
comments.
mstockstill on PROD1PC66 with NOTICES
AGENCY:
SUMMARY: The General Services
Administration (GSA) is proposing to
create a Federal Emergency Travel
Guide in the event of evacuation,
catastrophic event or natural disaster.
The guide is intended to prepare the
Federal Government to continue official
travel operations in an emergency
situation while safeguarding Federal
employees officially away from their
official or temporary duty stations. The
guide, non-regulatory in nature, will
serve as a supplement to the Federal
Travel Regulation (FTR) (41 CFR
chapters 300–304).
DATES: Please submit comments by
September 18, 2007.
ADDRESSES: Written comments should
be sent to Ms. Jane Groat, Travel Policy
Management (MTT), Office of
Governmentwide Policy, General
Services Administration, 1800 F Street,
NW., Washington, DC 20405. E-mail
comments may be sent to
perdiem@gsa.gov. Please entitle your
letter or e-mail with ‘‘Federal
Emergency Travel Guide comments’’.
VerDate Aug<31>2005
16:19 Jul 19, 2007
Jkt 211001
Jane
Groat, Travel Policy Management
(MTT), telephone 202–501–4318.
SUPPLEMENTARY INFORMATION: To access
the draft guide, you may visit https://
www.gsa.gov/travelpolicy (click
Library). A hard copy of the draft guide
is not available.
GSA is interested to learn from
Federal, (1) how to improve the draft
guide; (2) whether Federal agencies and
employees agree that the guide will be
a useful tool; (3) what Federal agencies
already have related policies in place
(and identify a web site)—employees on
site in support of an incident of
National significance are generally
under the effect of a National Response
Plan and follow those established
guides; (4) what kinds of things need to
be added to the guide for
governmentwide benefit; and (5) any
other related comment/suggestion.
If you comment, please include your
name, title, your capacity (i.e., an
employee, an official, or an Emergency
Response Team), telephone, agency,
email and hard addresses. Are you
commenting from personal experience
as a traveler, a supervisor/manager, or
an Emergency Response Team? Have
you had a need for emergency guides?
If you survived a horrific event or
emergency, what help/assistance was
needed the most, where did
expectations and support fall short, and
what would your recommendations be?
If you are a private sector travel or
transportation service provider to the
Government, we will also welcome your
comments.
FOR FURTHER INFORMATION CONTACT:
Dated: July 16, 2007.
Patrick Mc Connell,
Acting Director, Travel Policy Management.
[FR Doc. E7–14052 Filed 7–19–07; 8:45 am]
BILLING CODE 6820–14–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10224, CMS–
10240 and CMS–10052]
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
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
AGENCY:
PO 00000
Frm 00029
Fmt 4703
Sfmt 4703
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: New collection; Title of
Information Collection: HCPCS Level II
Code Modification Request Process;
Use: For Medicare and other health
insurance programs to ensure that
claims are processed in an orderly and
consistent manner, standardized coding
systems are essential. The Healthcare
Common Procedure Coding System
(HCPCS) Level II Code Set is one of the
standard code sets used for this
purpose. Level II of the HCPCS, also
referred to as alpha-numeric codes, is a
standardized coding system that is used
primarily to identify products, supplies,
and services not included in the Current
Procedural Terminology (CPT) codes,
such as ambulatory services and durable
medical equipment, prosthetics,
orthotics, and supplies (DMEPOS) when
used in the home or outpatient setting.
As technology evolves and new
products are developed, there are
continuous changes to the HCPCS
codeset. Modifications to the HCPCS are
initiated via application form submitted
by any interested stakeholder. These
applications have been received on an
on-going basis with an annual deadline
for each cycle. In October 2003, the
Secretary of Health and Human Services
delegated CMS authority to maintain
and distribute HCPCS Level II Codes. As
a result, the National Panel was
delineated and CMS continued with the
decision-making process under its
current structure, the CMS HCPCS
Workgroup.
CMS’ Council on Technological
Innovation (CTI) has instituted a
number of improvements to the HCPCS
process. Specific process refinements
include public notification of CMS’
preliminary decisions, and a new
opportunity to respond to CMS’
preliminary decisions at a public
meeting before a final decision is
reached by the workgroup. CMS has
streamlined the form into a userfriendly application. The content of the
material is the same, but the questions
E:\FR\FM\20JYN1.SGM
20JYN1
mstockstill on PROD1PC66 with NOTICES
Federal Register / Vol. 72, No. 139 / Friday, July 20, 2007 / Notices
have been refined. CMS is also
preparing a system of records (SOR)
notice.
Applications are received, and
distributed to all workgroup members.
Workgroup members review the
material and provide comments at the
HCPCS workgroup meetings.
Discussions are posted to CMS’ HCPCS
website. Final decisions are released to
the applicant via letter; and all resulting
modifications to the HCPCS codes are
reflected on the HCPCS update. Form
Number: CMS–10224 (OMB#: 0938–
New); Frequency: Reporting:
Occasionally; Affected Public: Business
or other for-profit and State, Local or
Tribal Government; Number of
Respondents: 300; Total Annual
Responses: 300; Total Annual Hours:
3,300.
2. Type of Information Collection
Request: New collection; Title of
Information Collection: Data Collection
for the Nursing Home Value-Based
Purchasing (NHVBP) Demonstration;
Use: The NHVBP Demonstration is a
CMS ‘‘pay-for-performance’’ initiative to
improve the quality of care furnished to
Medicare beneficiaries residing in
nursing homes. Under this three-year
demonstration project, CMS will assess
the performance of nursing homes based
on selected quality measures, and then
make additional payments to those
nursing homes that achieve a higher
performance based on those measures.
In the first year of the demonstration,
quality will be assessed based on the
following four domains: staffing,
appropriate hospitalizations, outcome
measures from the minimum data set
(MDS), and survey deficiencies.
Additional quality measures may be
added in the second and third years of
the demonstration as deemed
appropriate.
The main purpose of the NHVBP data
collection effort is to gather information
that will enable CMS to determine
which nursing homes will be eligible to
receive incentive payments under the
NHVBP Demonstration. All measures
included in the MDS outcomes, survey
deficiency, and appropriate
hospitalization domains can be
calculated from existing secondary data
sources, such as the MDS, annual
nursing home certification surveys, and
Medicare claims data. However, for the
staffing domain, no satisfactory
alternative source for these data has
been identified. Therefore, CMS will
collect payroll-based staffing and
resident census information to help
assess the quality of care in
participating nursing homes. CMS will
additionally collect data on two
measures, staff immunization status and
VerDate Aug<31>2005
16:19 Jul 19, 2007
Jkt 211001
use of resident care experience surveys,
which may be included in the payment
determination during the second and
third years of the demonstration. Form
Number: CMS–10240 (OMB#: 0938–
New); Frequency: Reporting: Once;
Affected Public: Business or other forprofit and not-for-profit institutions;
Number of Respondents: 1,250; Total
Annual Responses: 2,000; Total Annual
Hours: 49,170.
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Recognition of
pass-through payment for additional
(new) categories of devices under the
Outpatient Prospective Payment System
and Supporting Regulations in 42 CFR,
Part 419; Use: Section 201(b) of the
Balanced Budget Act of 1999 amended
section 1833(t) of the Social Security
Act (the Act) by adding new section
1833(t)(6). This provision requires the
Secretary to make additional payments
to hospitals for a period of 2 to 3 years
for certain drugs, radiopharmaceuticals,
biological agents, medical devices and
brachytherapy devices. Section
1833(t)(6)(A)(iv) establishes the criteria
for determining the application of this
provision to new items. Section
1833(t)(6)(C)(ii) provides that the
additional payment for medical devices
be the amount by which the hospital’s
charges for the device, adjusted to cost,
exceed the portion of the otherwise
applicable hospital outpatient
department fee schedule amount
determined by the Secretary to be
associated with the device. Section 402
of the Benefits Improvement and
Protection Act of 2000 made changes to
the transitional pass-through provision
for medical devices. The most
significant change is the required use of
categories as the basis for determining
transitional pass-through eligibility for
medical devices, through the addition of
section 1833(t)(6)(B) of the Act.
Interested parties such as hospitals,
device manufacturers, pharmaceutical
companies, and physicians apply for
transitional pass-through payment for
certain items used with services covered
in the outpatient prospective payment
system. After CMS receives all
requested information, CMS will
evaluate the information to determine if
the creation of an additional category of
medical devices for transitional passthrough payments is justified. Form
Number: CMS–10052 (OMB#: 0938–
0857); Frequency: Reporting: Yearly;
Affected Public: Business or other forprofit; Number of Respondents: 10;
Total Annual Responses: 10; Total
Annual Hours: 160.
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39813
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.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received at the address below, no
later than 5 p.m. on September 18, 2007.
CMS, Office of Strategic Operations
and Regulatory Affairs, Division of
Regulations Development—C, Attention:
Bonnie L Harkless, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: July 12, 2007.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E7–13904 Filed 7–19–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–244 and
CMS–18F5]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
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), Department of Health
and Human Services, 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 function;
(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
AGENCY:
E:\FR\FM\20JYN1.SGM
20JYN1
Agencies
[Federal Register Volume 72, Number 139 (Friday, July 20, 2007)]
[Notices]
[Pages 39812-39813]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-13904]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10224, CMS-10240 and CMS-10052]
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: New collection; Title of
Information Collection: HCPCS Level II Code Modification Request
Process; Use: For Medicare and other health insurance programs to
ensure that claims are processed in an orderly and consistent manner,
standardized coding systems are essential. The Healthcare Common
Procedure Coding System (HCPCS) Level II Code Set is one of the
standard code sets used for this purpose. Level II of the HCPCS, also
referred to as alpha-numeric codes, is a standardized coding system
that is used primarily to identify products, supplies, and services not
included in the Current Procedural Terminology (CPT) codes, such as
ambulatory services and durable medical equipment, prosthetics,
orthotics, and supplies (DMEPOS) when used in the home or outpatient
setting. As technology evolves and new products are developed, there
are continuous changes to the HCPCS codeset. Modifications to the HCPCS
are initiated via application form submitted by any interested
stakeholder. These applications have been received on an on-going basis
with an annual deadline for each cycle. In October 2003, the Secretary
of Health and Human Services delegated CMS authority to maintain and
distribute HCPCS Level II Codes. As a result, the National Panel was
delineated and CMS continued with the decision-making process under its
current structure, the CMS HCPCS Workgroup.
CMS' Council on Technological Innovation (CTI) has instituted a
number of improvements to the HCPCS process. Specific process
refinements include public notification of CMS' preliminary decisions,
and a new opportunity to respond to CMS' preliminary decisions at a
public meeting before a final decision is reached by the workgroup. CMS
has streamlined the form into a user-friendly application. The content
of the material is the same, but the questions
[[Page 39813]]
have been refined. CMS is also preparing a system of records (SOR)
notice.
Applications are received, and distributed to all workgroup
members. Workgroup members review the material and provide comments at
the HCPCS workgroup meetings. Discussions are posted to CMS' HCPCS
website. Final decisions are released to the applicant via letter; and
all resulting modifications to the HCPCS codes are reflected on the
HCPCS update. Form Number: CMS-10224 (OMB: 0938-New);
Frequency: Reporting: Occasionally; Affected Public: Business or other
for-profit and State, Local or Tribal Government; Number of
Respondents: 300; Total Annual Responses: 300; Total Annual Hours:
3,300.
2. Type of Information Collection Request: New collection; Title of
Information Collection: Data Collection for the Nursing Home Value-
Based Purchasing (NHVBP) Demonstration; Use: The NHVBP Demonstration is
a CMS ``pay-for-performance'' initiative to improve the quality of care
furnished to Medicare beneficiaries residing in nursing homes. Under
this three-year demonstration project, CMS will assess the performance
of nursing homes based on selected quality measures, and then make
additional payments to those nursing homes that achieve a higher
performance based on those measures. In the first year of the
demonstration, quality will be assessed based on the following four
domains: staffing, appropriate hospitalizations, outcome measures from
the minimum data set (MDS), and survey deficiencies. Additional quality
measures may be added in the second and third years of the
demonstration as deemed appropriate.
The main purpose of the NHVBP data collection effort is to gather
information that will enable CMS to determine which nursing homes will
be eligible to receive incentive payments under the NHVBP
Demonstration. All measures included in the MDS outcomes, survey
deficiency, and appropriate hospitalization domains can be calculated
from existing secondary data sources, such as the MDS, annual nursing
home certification surveys, and Medicare claims data. However, for the
staffing domain, no satisfactory alternative source for these data has
been identified. Therefore, CMS will collect payroll-based staffing and
resident census information to help assess the quality of care in
participating nursing homes. CMS will additionally collect data on two
measures, staff immunization status and use of resident care experience
surveys, which may be included in the payment determination during the
second and third years of the demonstration. Form Number: CMS-10240
(OMB: 0938-New); Frequency: Reporting: Once; Affected Public:
Business or other for-profit and not-for-profit institutions; Number of
Respondents: 1,250; Total Annual Responses: 2,000; Total Annual Hours:
49,170.
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Recognition of
pass-through payment for additional (new) categories of devices under
the Outpatient Prospective Payment System and Supporting Regulations in
42 CFR, Part 419; Use: Section 201(b) of the Balanced Budget Act of
1999 amended section 1833(t) of the Social Security Act (the Act) by
adding new section 1833(t)(6). This provision requires the Secretary to
make additional payments to hospitals for a period of 2 to 3 years for
certain drugs, radiopharmaceuticals, biological agents, medical devices
and brachytherapy devices. Section 1833(t)(6)(A)(iv) establishes the
criteria for determining the application of this provision to new
items. Section 1833(t)(6)(C)(ii) provides that the additional payment
for medical devices be the amount by which the hospital's charges for
the device, adjusted to cost, exceed the portion of the otherwise
applicable hospital outpatient department fee schedule amount
determined by the Secretary to be associated with the device. Section
402 of the Benefits Improvement and Protection Act of 2000 made changes
to the transitional pass-through provision for medical devices. The
most significant change is the required use of categories as the basis
for determining transitional pass-through eligibility for medical
devices, through the addition of section 1833(t)(6)(B) of the Act.
Interested parties such as hospitals, device manufacturers,
pharmaceutical companies, and physicians apply for transitional pass-
through payment for certain items used with services covered in the
outpatient prospective payment system. After CMS receives all requested
information, CMS will evaluate the information to determine if the
creation of an additional category of medical devices for transitional
pass-through payments is justified. Form Number: CMS-10052
(OMB: 0938-0857); Frequency: Reporting: Yearly; Affected
Public: Business or other for-profit; Number of Respondents: 10; Total
Annual Responses: 10; Total Annual Hours: 160.
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 E-mail 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.
To be assured consideration, comments and recommendations for the
proposed information collections must be received at the address below,
no later than 5 p.m. on September 18, 2007.
CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development--C, Attention: Bonnie L Harkless,
Room C4-26-05, 7500 Security Boulevard, Baltimore, Maryland 21244-1850.
Dated: July 12, 2007.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E7-13904 Filed 7-19-07; 8:45 am]
BILLING CODE 4120-01-P