Agency Information Collection Activities: Proposed Collection; Comment Request, 29156 [E6-7510]
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29156
Federal Register / Vol. 71, No. 97 / Friday, May 19, 2006 / Notices
M/S e–28, 1600 Clifton Road, NE., Atlanta,
Georgia 30333, telephone (404) 498–0622.
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 NCEH/ATSDR.
Dated: May 12, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 06–4694 Filed 5–18–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–262 and CMS
10196]
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
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: Extension of a currently
approved collection; Title of
Information Collection: Plan Benefit
Package (PBP) and Formulary
Submission for Medicare Advantage
(MA) Plans and Prescription Drug Plans
(PDPs); Use: Under the Medicare
Modernization Act (MMA), Medicare
Advantage (MA) and Prescription Drug
Plan (PDP) organizations are required to
submit plan benefit packages for all
Medicare beneficiaries residing in their
service area. CMS requires that MA and
PDP organizations submit a completed
wwhite on PROD1PC61 with NOTICES
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17:37 May 18, 2006
Jkt 208001
formulary and PBP as part of the annual
bidding process. During this process,
organizations prepare their proposed
plan benefit packages for the upcoming
contract year and submit them to CMS
for review and approval; Form Number:
CMS–R–262 (OMB#: 0938–0763);
Frequency: On occasion, Annually, and
Other: As required by new legislation;
Affected Public: Business or other forprofit and Not-for-profit institutions;
Number of Respondents: 553; Total
Annual Responses: 5,807; Total Annual
Hours: 13,272.
2. Type of Information Collection
Request: New Collection; Title of
Information Collection: Medicare Part C
Audit Guide, Version 4.0 and
Supporting Regulation contained in 42
CFR 423.502; Use™ The Medicare
Modernization Act provides CMS the
regulatory authority to audit, evaluate,
or inspect any Part C sponsors’
performance related to the law in the
areas including enrollment &
disenrollment, marketing, benefits and
beneficiary protections, quality
assurance, provider relations and
contracts. The information collected
will be an integral resource for
oversight, monitoring, compliance, and
auditing activities necessary to ensure
quality provision of the Part C Medicare
Advantage benefit to beneficiaries. Form
Number: CMS–10196 (OMB#: 0938New); Frequency: Recordkeeping and
Reporting—Annually; Affected Public:
Business or other for-profit; Number of
Respondents: 393; Total Annual
Responses: 393; Total Annual Hours:
12,576.
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 July 18, 2006.
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.
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
Dated: May 10, 2006.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E6–7510 Filed 5–18–06; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–718BP, 719BP,
720BP, 721BP, SUM, STAFFING, SC1 and
SC2]
Agency Information Collection
Activities: Submission for OMB
Review; 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
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: Business
Proposal Forms for Quality
Improvement Organizations (QIOs); Use:
The submission of proposal information
by current QIOs and other bidders, on
the appropriate forms, will satisfy
CMS’s need for meaningful, consistent,
and verifiable data with which to
evaluate contract proposals. The
Government will be able to compare the
costs reported by the QIOs on the cost
reports to the proposed costs noted on
the business proposal forms.
Subsequent contract and modification
negotiations will be based on historic
cost data. The business proposal forms
will be one element of the historical cost
data from which we can analyze future
AGENCY:
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[Federal Register Volume 71, Number 97 (Friday, May 19, 2006)]
[Notices]
[Page 29156]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-7510]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-R-262 and CMS 10196]
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: Extension of a currently
approved collection; Title of Information Collection: Plan Benefit
Package (PBP) and Formulary Submission for Medicare Advantage (MA)
Plans and Prescription Drug Plans (PDPs); Use: Under the Medicare
Modernization Act (MMA), Medicare Advantage (MA) and Prescription Drug
Plan (PDP) organizations are required to submit plan benefit packages
for all Medicare beneficiaries residing in their service area. CMS
requires that MA and PDP organizations submit a completed formulary and
PBP as part of the annual bidding process. During this process,
organizations prepare their proposed plan benefit packages for the
upcoming contract year and submit them to CMS for review and approval;
Form Number: CMS-R-262 (OMB: 0938-0763); Frequency: On
occasion, Annually, and Other: As required by new legislation; Affected
Public: Business or other for-profit and Not-for-profit institutions;
Number of Respondents: 553; Total Annual Responses: 5,807; Total Annual
Hours: 13,272.
2. Type of Information Collection Request: New Collection; Title of
Information Collection: Medicare Part C Audit Guide, Version 4.0 and
Supporting Regulation contained in 42 CFR 423.502; Use: The Medicare
Modernization Act provides CMS the regulatory authority to audit,
evaluate, or inspect any Part C sponsors' performance related to the
law in the areas including enrollment & disenrollment, marketing,
benefits and beneficiary protections, quality assurance, provider
relations and contracts. The information collected will be an integral
resource for oversight, monitoring, compliance, and auditing activities
necessary to ensure quality provision of the Part C Medicare Advantage
benefit to beneficiaries. Form Number: CMS-10196 (OMB: 0938-
New); Frequency: Recordkeeping and Reporting--Annually; Affected
Public: Business or other for-profit; Number of Respondents: 393; Total
Annual Responses: 393; Total Annual Hours: 12,576.
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 July 18, 2006.
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: May 10, 2006.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E6-7510 Filed 5-18-06; 8:45 am]
BILLING CODE 4120-01-P
