Agency Information Collection Activities: Proposed Collection; Comment Request, 43449-43450 [E8-17117]
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Federal Register / Vol. 73, No. 144 / Friday, July 25, 2008 / Notices
TO: Heads of Federal Agencies
SUBJECT: Relocation Allowances—
Standard Mileage Rate for Moving
Purposes
1. What is the purpose of this
bulletin? This bulletin informs agencies
that on June 23, 2008, the IRS
announced an eight cent increase in the
Standard Mileage Rate for moving
purposes from 19 cents to 27 cents per
mile. This new Standard Mileage Rate
for moving purposes is effective July 1,
2008, through December 31, 2008, and
applies to relocations undertaken by
Federal employees during this time
period.
2. What is the background of this
bulletin? On December 11, 2007, GSA
published FTR Amendment 2007–06 in
the Federal Register (72 FR 70234)
specifying that the IRS Standard
Mileage Rate for moving purposes
would be the rate at which agencies will
reimburse an employee for using a
privately owned vehicle (POV) for
relocation worldwide. The amendment
indicated that the change to the IRS
Standard Mileage Rate for moving
purposes applied to relocations on and
after September 25, 2007, and that GSA
would publish a bulletin announcing
any changes to that rate made by the IRS
thereafter.
3. Who should I call for further
information? For further information,
contact Mr. Ed Davis, Office of
Governmentwide Policy (M), Office of
Travel, Transportation, and Asset
Management (MT), General Services
Administration at (202) 208–7638 or via
e-mail at ed.davis@gsa.gov.
By delegation of the Administrator of
General Services,
Kevin Messner,
Acting Associate Administrator,
Office of Governmentwide Policy.
[FR Doc. E8–17091 Filed 7–24–08; 8:45 am]
BILLING CODE 6820–14–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
mstockstill on PROD1PC66 with NOTICES
[Document Identifier: CMS–10166, CMS–
10182, and CMS–846–849, 854, 10125,
10126, and 10269]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
AGENCY:
VerDate Aug<31>2005
17:15 Jul 24, 2008
Jkt 214001
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: Payment Error
Rate Measurement in Medicaid and the
State Children’s Health Insurance
Program (SCHIP); Use: The Improper
Payments Information Act (IPIA) of
2002 requires CMS to produce national
error rates for Medicaid and State
Children’s Health Insurance Program
(SCHIP). To comply with the IPIA, CMS
will engage a Federal contractor to
produce the error rates in Medicaid and
SCHIP.
The states will be requested to submit,
at their option, test data which include
full claims details to the contractor prior
to the quarterly submissions to detect
potential problems in the dataset to and
ensure the quality of the data. These
states will be required to submit
quarterly claims data to the contractor
who will pull a statistically valid
random sample, each quarter, by strata,
so that medical and data processing
reviews can be performed. State-specific
error rates will be based on these review
results.
CMS needs to collect the claims data,
medical policies, and other information
from states as well as medical records
from providers in order for the
contractor to sample and review
adjudicated claims in those states
selected for review. Based on the
reviews, state-specific error rates will be
calculated which will serve as the basis
for calculating national Medicaid and
SCHIP error rates.
This revision of the currently
approved collection contains minor
revisions to the information collection
requirements. There is a 10-hour
increase in burden per state per program
as part of a new process. Based on the
past experience in PERM operation, the
adjustment is made to ensure the quality
of the data will comply with the data
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
43449
requirement during the measurement.
Form Number: CMS–10166 (OMB#
0938–0974); Frequency: Quarterly,
Yearly; Affected Public: State, Local or
Tribal Governments; Number of
Respondents: 34; Total Annual
Responses: 4,080; Total Annual Hours:
28,560.
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Model
Creditable Coverage Disclosure Notices;
Use: Section 1860D–1 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003 (MMA) and
implementing regulations at 42 CFR
423.56 require that entities that offer
prescription drug benefits under any of
the types of coverage described in 42
CFR 423.56(b) provide a disclosure of
creditable coverage status to all
Medicare Part D eligible individuals
covered under the entity’s plan
informing them whether such coverage
meets the actuarial requirements
specified in guidelines provided by
CMS.
These disclosure notices must be
provided to Part D eligible individuals,
at minimum, at the following times: (1)
Prior to an individual’s initial
enrollment period for Part D, as
described under § 423.38(a); (2) prior to
the effective date of enrollment in the
entity’s coverage, and upon any change
in creditable status; (3) prior to the
commencement of the Part D Annual
Coordinated Election Period (ACEP)
which begins on November 15 of each
year, as defined in § 423.38(b); and (4)
upon request by the individual. In an
effort to reduce the burden associated
with providing these notices, our final
regulations allow most entities to
provide notices of creditable and noncreditable status with other information
materials that these entities distribute to
beneficiaries.
This collection has been updated by
eliminating the separate Model
Personalized Disclosure Notice. CMS
has incorporated the personalized
information into the Model Creditable
Disclosure Notice and the Model NonCreditable Disclosure Notice for use by
the public. Form Number: CMS–10182
(OMB# 0938–0990); Frequency: Yearly
and Semi-annually; Affected Public:
Federal Government, Business or Other
For-Profits and Not-for-Profit
Institutions, and State, Local or Tribal
Governments; Number of Respondents:
1,225,173; Total Annual Responses:
1,225,173; Total Annual Hours: 522,204.
3. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Durable Medical
E:\FR\FM\25JYN1.SGM
25JYN1
mstockstill on PROD1PC66 with NOTICES
43450
Federal Register / Vol. 73, No. 144 / Friday, July 25, 2008 / Notices
Equipment Medicare Administrative
Contractors (MAC), Certificates of
Medical Necessity; Use: The certificate
of medical necessity (CMN) collects
information required to help determine
the medical necessity of certain items.
CMS requires CMNs where there may be
a vulnerability to the Medicare program.
Each initial claim for these items must
have an associated CMN for the
beneficiary. Suppliers (those who bill
for the items) complete the
administrative information (e.g.,
patient’s name and address, items
ordered, etc.) on each CMN. The 1994
Amendments to the Social Security Act
require that the supplier also provide a
narrative description of the items
ordered and all related accessories, their
charge for each of these items, and the
Medicare fee schedule allowance (where
applicable). The supplier then sends the
CMN to the treating physician or other
clinicians (e.g., physician assistant,
LPN, etc.) who completes questions
pertaining to the beneficiary’s medical
condition and signs the CMN. The
physician or other clinician returns the
CMN to the supplier who has the option
to maintain a copy and then submits the
CMN (paper or electronic) to CMS,
along with a claim for reimbursement.
Form Number: CMS–846–849, 854,
10125, 10126, 10269 (OMB# 0938–
0679); Frequency: Occasionally;
Affected Public: Business or other forprofit and Not-for-profit institutions;
Number of Respondents: 59,200; Total
Annual Responses: 6,480,000; Total
Annual Hours: 1,296,000.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
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 September 23, 2008:
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
VerDate Aug<31>2005
17:15 Jul 24, 2008
Jkt 214001
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number llllll, Room
C4–26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Dated: July 18, 2008.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E8–17117 Filed 7–24–08; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–1396–N]
Medicare Program; Announcement of
Three New Members to the Advisory
Panel on Ambulatory Payment
Classification (APC) Groups
Centers for Medicare &
Medicaid Services (CMS), Department
of Health and Human Services (DHHS).
ACTION: Notice.
AGENCY:
SUMMARY: This notice announces three
new members selected to serve on the
Advisory Panel on Ambulatory Payment
Classification (APC) Groups (the Panel).
The purpose of the Panel is to review
the APC groups and their associated
weights and to advise the Secretary,
DHHS (the Secretary), and the
Administrator, CMS (the
Administrator), concerning the clinical
integrity of the APC groups and their
associated weights. We will consider the
Panel’s advice as we prepare the annual
updates of the hospital outpatient
prospective payment system (OPPS).
FOR FURTHER INFORMATION CONTACT: For
inquiries about the Panel, please contact
the Designated Federal Official (DFO):
Shirl Ackerman-Ross, DFO, CMS, CMM,
HAPG, DOC, 7500 Security Boulevard,
Mail Stop C4–05–17, Baltimore, MD
21244–1850. Phone (410) 786–4474.
APC Panel E-Mail Address: The Email address for the Panel is as follows:
CMS APCPanel@cms.hhs.gov.
Note: There is NO underscore in this email address; there is a SPACE between CMS
and APCPanel.
News Media Contact: News media
representatives must contact our Public
Affairs Office at (202) 690–6145.
CMS Advisory Committees Hotlines:
The CMS Federal Advisory Committee
Hotline is 1–877–449–5659 (toll free)
and (410) 786–9379 (local) for
additional Panel information.
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
Web Sites: For additional information
regarding the APC Panel membership,
meetings, agendas, and updates to the
Panel’s activities, please search our Web
site at the following Uniform Resource
Locator (URL): https://www.cms.hhs.gov/
FACA/05_AdvisoryPanelonAmbulatory
PaymentClassificationGroups.asp#
TopOfPage.
Note: There is an underscore after FACA/
05 (like this _); there is no space.
The public may also access the
following URL for the Federal Advisory
Committee Act Web site to obtain APC
Panel information: https://
www.fido.gov/facadatabase/logon.asp.
A copy of the Panel’s Charter and other
pertinent information are on both Web
sites mentioned above. You may also email the Panel DFO at the above e-mail
address for a copy of the Charter.
SUPPLEMENTARY INFORMATION:
I. Background
The Secretary is required by section
1833(t)(9)(A) of the Social Security Act
(the Act), as amended and redesignated
by sections 201(h) and 202(a)(2) of the
Medicare, Medicaid, and SCHIP
Balanced Budget Refinement Act of
1999 (BBRA) (Pub. L. 106–113), to
consult with an expert outside advisory
Panel regarding the clinical integrity of
the APC groups and relative payment
weights that are components of the
Medicare hospital OPPS.
The APC Panel meets up to three
times annually. The Charter requires
that the Panel must be fairly balanced in
its membership in terms of the points of
view represented and the functions to
be performed. The Panel consists of up
to 15 members, who are representatives
of providers, and a Chair. Each Panel
member must be employed full-time by
a hospital, hospital system, or other
Medicare provider subject to payment
under the OPPS. The Secretary or
Administrator selects the Panel
membership based upon either selfnominations or nominations submitted
by Medicare providers and other
interested organizations. All members
must have technical expertise to enable
them to participate fully in the work of
the Panel. This expertise encompasses
hospital payment systems; hospital
medical-care delivery systems; provider
billing systems; APC groups, Current
Procedural Terminology codes, and
alpha-numeric Healthcare Common
Procedure Coding System codes; and
the use and payment of drugs and
medical devices in the outpatient
setting, as well as other forms of
relevant expertise.
The Charter requires that all members
have a minimum of 5 years experience
E:\FR\FM\25JYN1.SGM
25JYN1
Agencies
[Federal Register Volume 73, Number 144 (Friday, July 25, 2008)]
[Notices]
[Pages 43449-43450]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-17117]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10166, CMS-10182, and CMS-846-849, 854,
10125, 10126, and 10269]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services.
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: Payment Error
Rate Measurement in Medicaid and the State Children's Health Insurance
Program (SCHIP); Use: The Improper Payments Information Act (IPIA) of
2002 requires CMS to produce national error rates for Medicaid and
State Children's Health Insurance Program (SCHIP). To comply with the
IPIA, CMS will engage a Federal contractor to produce the error rates
in Medicaid and SCHIP.
The states will be requested to submit, at their option, test data
which include full claims details to the contractor prior to the
quarterly submissions to detect potential problems in the dataset to
and ensure the quality of the data. These states will be required to
submit quarterly claims data to the contractor who will pull a
statistically valid random sample, each quarter, by strata, so that
medical and data processing reviews can be performed. State-specific
error rates will be based on these review results.
CMS needs to collect the claims data, medical policies, and other
information from states as well as medical records from providers in
order for the contractor to sample and review adjudicated claims in
those states selected for review. Based on the reviews, state-specific
error rates will be calculated which will serve as the basis for
calculating national Medicaid and SCHIP error rates.
This revision of the currently approved collection contains minor
revisions to the information collection requirements. There is a 10-
hour increase in burden per state per program as part of a new process.
Based on the past experience in PERM operation, the adjustment is made
to ensure the quality of the data will comply with the data requirement
during the measurement. Form Number: CMS-10166 (OMB 0938-
0974); Frequency: Quarterly, Yearly; Affected Public: State, Local or
Tribal Governments; Number of Respondents: 34; Total Annual Responses:
4,080; Total Annual Hours: 28,560.
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Model Creditable
Coverage Disclosure Notices; Use: Section 1860D-1 of the Medicare
Prescription Drug, Improvement, and Modernization Act of 2003 (MMA) and
implementing regulations at 42 CFR 423.56 require that entities that
offer prescription drug benefits under any of the types of coverage
described in 42 CFR 423.56(b) provide a disclosure of creditable
coverage status to all Medicare Part D eligible individuals covered
under the entity's plan informing them whether such coverage meets the
actuarial requirements specified in guidelines provided by CMS.
These disclosure notices must be provided to Part D eligible
individuals, at minimum, at the following times: (1) Prior to an
individual's initial enrollment period for Part D, as described under
Sec. 423.38(a); (2) prior to the effective date of enrollment in the
entity's coverage, and upon any change in creditable status; (3) prior
to the commencement of the Part D Annual Coordinated Election Period
(ACEP) which begins on November 15 of each year, as defined in Sec.
423.38(b); and (4) upon request by the individual. In an effort to
reduce the burden associated with providing these notices, our final
regulations allow most entities to provide notices of creditable and
non-creditable status with other information materials that these
entities distribute to beneficiaries.
This collection has been updated by eliminating the separate Model
Personalized Disclosure Notice. CMS has incorporated the personalized
information into the Model Creditable Disclosure Notice and the Model
Non-Creditable Disclosure Notice for use by the public. Form Number:
CMS-10182 (OMB 0938-0990); Frequency: Yearly and Semi-
annually; Affected Public: Federal Government, Business or Other For-
Profits and Not-for-Profit Institutions, and State, Local or Tribal
Governments; Number of Respondents: 1,225,173; Total Annual Responses:
1,225,173; Total Annual Hours: 522,204.
3. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Durable Medical
[[Page 43450]]
Equipment Medicare Administrative Contractors (MAC), Certificates of
Medical Necessity; Use: The certificate of medical necessity (CMN)
collects information required to help determine the medical necessity
of certain items. CMS requires CMNs where there may be a vulnerability
to the Medicare program. Each initial claim for these items must have
an associated CMN for the beneficiary. Suppliers (those who bill for
the items) complete the administrative information (e.g., patient's
name and address, items ordered, etc.) on each CMN. The 1994 Amendments
to the Social Security Act require that the supplier also provide a
narrative description of the items ordered and all related accessories,
their charge for each of these items, and the Medicare fee schedule
allowance (where applicable). The supplier then sends the CMN to the
treating physician or other clinicians (e.g., physician assistant, LPN,
etc.) who completes questions pertaining to the beneficiary's medical
condition and signs the CMN. The physician or other clinician returns
the CMN to the supplier who has the option to maintain a copy and then
submits the CMN (paper or electronic) to CMS, along with a claim for
reimbursement. Form Number: CMS-846-849, 854, 10125, 10126, 10269
(OMB 0938-0679); Frequency: Occasionally; Affected Public:
Business or other for-profit and Not-for-profit institutions; Number of
Respondents: 59,200; Total Annual Responses: 6,480,000; Total Annual
Hours: 1,296,000.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web Site 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.
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 September 23, 2008:
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.
Dated: July 18, 2008.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E8-17117 Filed 7-24-08; 8:45 am]
BILLING CODE 4120-01-P