Agency Information Collection Activities: Submission for OMB Review; Comment Request, 30421-30422 [E6-7944]
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Federal Register / Vol. 71, No. 102 / Friday, May 26, 2006 / Notices
Status:
Open 8 a.m.–8:30 a.m., June 13, 2006.
Closed 8:30 a.m.–5 p.m., June 13, 2006.
Closed 8:30 a.m.–5 p.m., June 14, 2006.
Purpose: The Safety and Occupational
Health Study Section will review, discuss,
and evaluate grant application(s) received in
response to the Institute’s standard grants
review and funding cycles pertaining to
research issues in occupational safety and
health and allied areas.
It is the intent of the Institute to support
broad-based research endeavors in keeping
their program goals. This will lead to
improved understanding and appreciation for
the magnitude of the aggregate health burden
associated with occupational injuries and
illnesses, as well as to support more focused
research projects, which will lead to
improvements in the delivery of occupational
safety and health services, and the
prevention of work-related injury and illness.
It is anticipated that research funding will
promote these program goals.
Matters to be Discussed: The meeting will
convene in open session from 8 a.m.–8:30
a.m. on June 13, 2006, to address matters
related to the conduct of Study Section
business. The remainder of the meeting will
proceed in closed session. The purpose of the
closed session is for the study section to
consider safety and occupational healthrelated grant applications. These portions of
the meeting will be closed to the public in
accordance with provisions set forth in
section 552b(c)(4) and (6), Title 5 U.S.C., and
the Determination of the Director,
Management Analysis and Services Office,
Centers for Disease Control and Prevention,
pursuant to section 10(d) Public Law 92–463.
Agenda items are subject to change as
priorities dictate.
For Further Information Contact: Price
Connor, Ph.D., NIOSH Health Scientist, 1600
Clifton Road, NE., Mailstop E–20, Atlanta,
Georgia 30333, telephone 404.498.2511, fax
404.498.2569.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities for
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: May 22, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–8126 Filed 5–25–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–668B, CMS–R–
284, CMS–R–205, CMS–10187, and CMS–
10116]
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
minimize the information collection
burden.
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Post Clinical
Laboratory Survey Questionnaire and
Supporting Regulations in 42 CFR
493.1771, 493.1773, and 493.1777; Use:
To provide an opportunity and a
mechanism for Clinical Laboratory
Improvement Amendments of 1988
(CLIA) laboratories surveyed by CMS or
CMS’ agents to express their satisfaction
and concerns about the CLIA survey
process.; Form Number: CMS–668B
(OMB#: 0938–0653); Frequency:
Recordkeeping, Reporting—Biennially;
Affected Public: Business or other forprofit and Not-for-profit institutions;
Number of Respondents: 21,000; Total
Annual Responses: 10,500; Total
Annual Hours: 2,625.
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Medicaid
Statistical Information System; Use:
State data are reported by the Federally
mandated electronic process, known as
Medicaid Statistical Information System
(MSIS). These data are the basis of
AGENCY:
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30421
actuarial forecasts for Medicaid service
utilization and costs; of analysis and
cost savings estimates required for
legislative initiatives relating to
Medicaid; and for responding to
requests for information from CMS
components, the Department, Congress
and other customers.; Form Number:
CMS–R–284 (OMB#: 0938–0345);
Frequency: Quarterly; Affected Public:
State, Local or Tribal Government;
Number of Respondents: 53; Total
Annual Responses: 212; Total Annual
Hours: 2,120.
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Information
Collection Requirements Referenced in
HIPAA, Title 1 for the Individual
Market, supporting regulations at 45
CFR 148.120, 148.122, 148.124, 148.126,
and 148.128, and Forms/instructions;
Use: The provisions of Title I of the
Health Insurance Portability and
Accountability Act of 1996 (HIPAA)
amend the Public Health Service Act
(PHS Act) and are designed to make it
easier for people to get access to health
care coverage, reduce the limitations
that can be put on the coverage, and
limit the issuers’ ability to terminate
coverage. This information collection
requirement will ensure that issuers in
the individual market comply with Title
1 of HIPAA, provide individuals with
certificates of creditable coverage
necessary to demonstrate prior
creditable coverage, file the necessary
documentation with CMS for review in
States that have Federal direct
enforcement, and ensure States’
flexibility to implement State alternative
mechanisms. Individuals and their
dependents need certificates of
creditable coverage to take advantage of
the rights they have under HIPAA.
States and CMS need the information
supplied by issuers to properly perform
their regulatory functions under HIPAA
and or existing State law.; Form
Number: CMS–R–205 (OMB#: 0938–
0703); Frequency: Recordkeeping, Third
party disclosure, and Reporting—On
Occasion; Affected Public: Individuals
or Households, Business or other forprofit, Not-for-profit institutions and
Federal, State, Local or Tribal
Government; Number of Respondents:
1,042; Total Annual Responses:
2,987,501; Total Annual Hours: 868,147.
4. Type of Information Collection
Request: New collection; Title of
Information Collection: Evaluation of
the Demonstration of Coverage of
Chiropractic Services Under Medicare;
Use: Section 651 of the Medicare
Prescription Drug, Improvement and
Modernization Act of 2003, authorizes a
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Federal Register / Vol. 71, No. 102 / Friday, May 26, 2006 / Notices
two-year demonstration ‘‘to evaluate the
feasibility and advisability of covering
chiropractic services under Medicare’’.
The Demonstration aims to evaluate
both the costs and the benefits of
expanded coverage for chiropractic
services. The evaluation will examine
the achievements as well as the
difficulties inherent in demonstration
implementation. The study includes a
descriptive evaluation of the program, a
survey of a total of 2,000 beneficiaries
using expanded services, analyses of
medical claims to determine service
utilization and expenditures, as well as
the cost impact on the Medicare
program. These data will allow the
researchers to examine use,
effectiveness, and satisfaction of
Medicare beneficiaries with the
chiropractic services they receive in
relation to their demographic and
clinical characteristics. The results will
help CMS to understand the user’s
experience with chiropractic services
and with this Medicare demonstration.;
Form Number: CMS–10187 (OMB#:
0938-New); Frequency: Reporting—
Monthly; Affected Public: Individuals or
Households; Number of Respondents:
2000; Total Annual Responses: 2000;
Total Annual Hours: 667.
5. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Conditions of
Payment of Power Mobility Devices,
including Power Wheelchairs and
Power-Operated Vehicles (CMS–3017–
IFC); Use: CMS–3017–IFC (Conditions
for Payment of Power Mobility Devices,
including Power Wheelchairs and
Power-Operated Vehicles) provides
further guidance with respect to the
prescribing of and payment for Power
Mobility Devices (PMDs). This rule
defines the term power mobility devices
(PMDs) as power wheelchairs and
power operated vehicles (POVs or
scooters). This rule conforms our
regulations to section 302(a)(2)(E)(iv) of
the Medicare Prescription Drug,
Improvement, and Modernization Act of
2003 (MMA). The MMA mandated: (1)
A face-to-face examination of the
individual be conducted by a physician
(as defined in section 1861(r)(1) of the
Social Security Act (the Act)), a
physician assistant, a nurse practitioner
or a clinical nurse specialist (as those
terms are defined in section 1861(aa)(5)
of the Act; and (2) that payment may not
be made for a power wheelchair unless
the physician or treating practitioner
has written a prescription for the item.
With this information collection
request, CMS is seeking approval for the
collection requirements associated with
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CMS–3017–IFC (70 FR 50940).; Form
Number: CMS–10116 (OMB#: 0938–
0971); Frequency: Recordkeeping and
Reporting—On occasion; Affected
Public: Business or other for-profit, Notfor-profit institutions, Federal
government, State, Local, or Tribal
governments; Number of Respondents:
17,000; Total Annual Responses:
37,400; Total Annual Hours: 37,400.
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.
Written comments and
recommendations for the proposed
information collections must be mailed
or faxed within 30 days of this notice
directly to the OMB desk officer: OMB
Human Resources and Housing Branch,
Attention: Carolyn Lovett, New
Executive Office Building, Room 10235,
Washington, DC 20503. Fax Number:
(202) 395–6974.
Dated: May 15, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E6–7944 Filed 5–25–06; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–4117–FN]
Medicare Program; Approval of URAC
for Deeming Authority for Medicare
Advantage Health Maintenance
Organizations and Local Preferred
Provider Organizations
Centers for Medicare &
Medicaid Services (CMS), HHS.
ACTION: Final notice.
AGENCY:
SUMMARY: This final notice announces
the approval of URAC for deeming
authority as a national accreditation
organization for health maintenance
organizations and local preferred
provider organizations participating in
the Medicare Advantage program, for a
term of 6 years upon publication of this
notice in the Federal Register. This
notice describes the processes and
criteria used in evaluating the
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application. We did not receive any
public comments during the public
comment period, which ended on April
28, 2006.
FOR FURTHER INFORMATION CONTACT:
Shaheen Halim, Ph.D., (410) 786–0641.
I. Background
Under the Medicare program, eligible
beneficiaries may receive covered
services through a managed care
organization (MCO) that has a Medicare
Advantage (MA) (formerly,
Medicare+Choice) contract with the
Centers for Medicare & Medicaid
Services (CMS). The regulations
specifying the Medicare requirements
that must be met in order for an MCO
to enter into an MA contract with CMS
are located at 42 CFR part 422. These
regulations implement Part C of Title
XVIII of the Social Security Act (the
Act), which specifies the services that
an MCO must provide and the
requirements that the organization must
meet to be an MA contractor. Other
relevant sections of the Act are Parts A
and B of Title XVIII and Part A of Title
XI pertaining to the provision of
services by Medicare-certified providers
and suppliers.
Generally, for an organization to enter
into an MA contract, the organization
must be licensed by the State as a riskbearing organization as set forth in part
422 of our regulations. Additionally, the
organization must file an application
demonstrating that it meets other
Medicare requirements in part 422 of
our regulations. Following approval of
the contract, we engage in routine
monitoring and oversight audits of the
MA organization to ensure continuing
compliance. The monitoring and
oversight audit process is
comprehensive and uses a written
protocol that itemizes the Medicare
requirements the MA organization must
meet.
As an alternative for meeting some
Medicare requirements, an MA
organization may be exempt from our
monitoring of certain requirements in
subsets listed in section 1852(e)(4)(B) of
the Act as a result of an MA
organization’s accreditation by a CMSapproved accrediting organization (AO).
In essence, the Secretary ‘‘deems’’ that
the Medicare requirements are met
based on a determination that the AO’s
standards are at least as stringent as
Medicare requirements.
An organization that applies for MA
deeming authority is generally
recognized by the industry as an entity
that accredits MCOs that are licensed as
a health maintenance organization
(HMO) or a preferred provider
organization (PPO). As we specify at
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Agencies
[Federal Register Volume 71, Number 102 (Friday, May 26, 2006)]
[Notices]
[Pages 30421-30422]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-7944]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-668B, CMS-R-284, CMS-R-205, CMS-10187, and
CMS-10116]
Agency Information Collection Activities: Submission for OMB
Review; 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), 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 minimize the information
collection burden.
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Post Clinical
Laboratory Survey Questionnaire and Supporting Regulations in 42 CFR
493.1771, 493.1773, and 493.1777; Use: To provide an opportunity and a
mechanism for Clinical Laboratory Improvement Amendments of 1988 (CLIA)
laboratories surveyed by CMS or CMS' agents to express their
satisfaction and concerns about the CLIA survey process.; Form Number:
CMS-668B (OMB: 0938-0653); Frequency: Recordkeeping,
Reporting--Biennially; Affected Public: Business or other for-profit
and Not-for-profit institutions; Number of Respondents: 21,000; Total
Annual Responses: 10,500; Total Annual Hours: 2,625.
2. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Medicaid
Statistical Information System; Use: State data are reported by the
Federally mandated electronic process, known as Medicaid Statistical
Information System (MSIS). These data are the basis of actuarial
forecasts for Medicaid service utilization and costs; of analysis and
cost savings estimates required for legislative initiatives relating to
Medicaid; and for responding to requests for information from CMS
components, the Department, Congress and other customers.; Form Number:
CMS-R-284 (OMB: 0938-0345); Frequency: Quarterly; Affected
Public: State, Local or Tribal Government; Number of Respondents: 53;
Total Annual Responses: 212; Total Annual Hours: 2,120.
3. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Information
Collection Requirements Referenced in HIPAA, Title 1 for the Individual
Market, supporting regulations at 45 CFR 148.120, 148.122, 148.124,
148.126, and 148.128, and Forms/instructions; Use: The provisions of
Title I of the Health Insurance Portability and Accountability Act of
1996 (HIPAA) amend the Public Health Service Act (PHS Act) and are
designed to make it easier for people to get access to health care
coverage, reduce the limitations that can be put on the coverage, and
limit the issuers' ability to terminate coverage. This information
collection requirement will ensure that issuers in the individual
market comply with Title 1 of HIPAA, provide individuals with
certificates of creditable coverage necessary to demonstrate prior
creditable coverage, file the necessary documentation with CMS for
review in States that have Federal direct enforcement, and ensure
States' flexibility to implement State alternative mechanisms.
Individuals and their dependents need certificates of creditable
coverage to take advantage of the rights they have under HIPAA. States
and CMS need the information supplied by issuers to properly perform
their regulatory functions under HIPAA and or existing State law.; Form
Number: CMS-R-205 (OMB: 0938-0703); Frequency: Recordkeeping,
Third party disclosure, and Reporting--On Occasion; Affected Public:
Individuals or Households, Business or other for-profit, Not-for-profit
institutions and Federal, State, Local or Tribal Government; Number of
Respondents: 1,042; Total Annual Responses: 2,987,501; Total Annual
Hours: 868,147.
4. Type of Information Collection Request: New collection; Title of
Information Collection: Evaluation of the Demonstration of Coverage of
Chiropractic Services Under Medicare; Use: Section 651 of the Medicare
Prescription Drug, Improvement and Modernization Act of 2003,
authorizes a
[[Page 30422]]
two-year demonstration ``to evaluate the feasibility and advisability
of covering chiropractic services under Medicare''. The Demonstration
aims to evaluate both the costs and the benefits of expanded coverage
for chiropractic services. The evaluation will examine the achievements
as well as the difficulties inherent in demonstration implementation.
The study includes a descriptive evaluation of the program, a survey of
a total of 2,000 beneficiaries using expanded services, analyses of
medical claims to determine service utilization and expenditures, as
well as the cost impact on the Medicare program. These data will allow
the researchers to examine use, effectiveness, and satisfaction of
Medicare beneficiaries with the chiropractic services they receive in
relation to their demographic and clinical characteristics. The results
will help CMS to understand the user's experience with chiropractic
services and with this Medicare demonstration.; Form Number: CMS-10187
(OMB: 0938-New); Frequency: Reporting--Monthly; Affected
Public: Individuals or Households; Number of Respondents: 2000; Total
Annual Responses: 2000; Total Annual Hours: 667.
5. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: Conditions of
Payment of Power Mobility Devices, including Power Wheelchairs and
Power-Operated Vehicles (CMS-3017-IFC); Use: CMS-3017-IFC (Conditions
for Payment of Power Mobility Devices, including Power Wheelchairs and
Power-Operated Vehicles) provides further guidance with respect to the
prescribing of and payment for Power Mobility Devices (PMDs). This rule
defines the term power mobility devices (PMDs) as power wheelchairs and
power operated vehicles (POVs or scooters). This rule conforms our
regulations to section 302(a)(2)(E)(iv) of the Medicare Prescription
Drug, Improvement, and Modernization Act of 2003 (MMA). The MMA
mandated: (1) A face-to-face examination of the individual be conducted
by a physician (as defined in section 1861(r)(1) of the Social Security
Act (the Act)), a physician assistant, a nurse practitioner or a
clinical nurse specialist (as those terms are defined in section
1861(aa)(5) of the Act; and (2) that payment may not be made for a
power wheelchair unless the physician or treating practitioner has
written a prescription for the item. With this information collection
request, CMS is seeking approval for the collection requirements
associated with CMS-3017-IFC (70 FR 50940).; Form Number: CMS-10116
(OMB: 0938-0971); Frequency: Recordkeeping and Reporting--On
occasion; Affected Public: Business or other for-profit, Not-for-profit
institutions, Federal government, State, Local, or Tribal governments;
Number of Respondents: 17,000; Total Annual Responses: 37,400; Total
Annual Hours: 37,400.
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.
Written comments and recommendations for the proposed information
collections must be mailed or faxed within 30 days of this notice
directly to the OMB desk officer: OMB Human Resources and Housing
Branch, Attention: Carolyn Lovett, New Executive Office Building, Room
10235, Washington, DC 20503. Fax Number: (202) 395-6974.
Dated: May 15, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E6-7944 Filed 5-25-06; 8:45 am]
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