Agency Information Collection Activities: Submission for OMB Review; Comment Request, 57631-57632 [E8-23415]
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Federal Register / Vol. 73, No. 193 / Friday, October 3, 2008 / Notices
executive, physician, and clinical
engagement. Hospitals leaders will take
the HLQAT instrument via Web-based
technology. This function will be
carried out in conjunction with CMS
and the Quality Improvement
Organization (QIO) 9th Scope of Work
(SOW), to convey the importance of this
effort in relation to Medicare and other
public priorities. This administration of
the HLQAT seeks responses from
approximately a dozen leaders in each
hospital, including physicians (e.g.,
CEO, CMO), board members, directorlevel, and mid-level clinical managers—
these responses can provide a multilevel representation of hospital
leadership showing its commitment to
institutional change. Form Number:
CMS–10272 (OMB# 0938–New);
Frequency: Occasionally; Affected
Public: Private Sector—Business or
Other for-profits; Number of
Respondents: 18,000; Total Annual
Responses: 36,000; Total Annual Hours:
44,820.
4. Type of Information Collection
Request: New collection; Title of
Information Collection: Emergency and
Non-Emergency Ambulance Transports
and Beneficiary Signature Requirements
in 42 CFR 424.36(b); Use: In the CY
2008 Physician Fee Schedule (PFS) final
rule with comment period, we created
an additional exception to the
beneficiary signature requirements in
§ 424.36(b) for emergency ambulance
transports (72 FR 66406). The exception
allows ambulance providers and
suppliers to sign the claim on behalf of
the beneficiary, at the time of transport,
provided that certain documentation
requirements are met. Following
publication of the CY 2008 PFS final
rule with comment period, ambulance
provider and supplier stakeholders
requested that we extend the exception
in § 424.36(b)(6) to non-emergency
ambulance transports, in instances
where the beneficiary is physically or
mentally incapable of signing the claim
form.
The current submission of this
information collection request relates to
the collection of documentation
pertaining to non-emergency ambulance
transports. In addition, we are updating
the collection of information that relates
to the collection of documentation
pertaining to emergency ambulance
transports. Form Number: CMS–10242
(OMB# 0938–1049); Frequency:
Occasionally; Affected Public: Private
Sector—Business or Other for-profits
and Not-for-profit institutions; Number
of Respondents: 9,000; Total Annual
Responses: 13,185,835; Total Annual
Hours: 1,098,819.
VerDate Aug<31>2005
23:33 Oct 02, 2008
Jkt 217001
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 December 2, 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 lll, Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: September 26, 2008.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E8–23414 Filed 10–2–08; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10261, CMS–
10182, CMS–10166 and CMS–10150]
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
AGENCY:
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
57631
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: New collection; Title of
Information Collection: Part C Medicare
Advantage (MA) Reporting
Requirements and Supporting
Regulations in 42 CFR 422.516 (a); Use:
CMS has authority to establish reporting
requirements for Medicare Advantage
Organizations (MAOs) as described in
42 CFR 422.516(a). Under that authority,
each MAO must have an effective
procedure to develop, compile,
evaluate, and report to CMS, to its
enrollees, and to the general public, at
the times and in the manner that CMS
requires, and while safeguarding the
confidentiality of the doctor-patient
relationship, statistics and other
information with respect to the cost of
its operations, patterns of service
utilization, availability, accessibility,
and acceptability of its services,
developments in the health status of its
enrollees, and other matters that CMS
may require.
CMS will not require cost plans to
comply with the following reporting
requirements: Benefit utilization;
procedure frequency; and serious
reportable adverse events. However,
CMS has determined that it is essential
that all beneficiaries understand rules
and requirements of the Medicare plans
which they are being invited to join.
Prospective enrollees in cost plans
should be furnished accurate
information by qualified sales people,
consistent with CMS’ expectation for
prospective enrollees in other play
types. Thus, CMS is requiring reporting
on certain measures CMS’ believes is
critical in monitoring cost plans.
Additionally, CMS believes that section
1876(i)(1)(D) of the Act, and 42 CFR
417.126(a)(6) permits CMS to require
cost plans to report to CMS the data
identified as follows: Provider network
adequacy; grievances; organization
determinations/reconsiderations;
employer group plan sponsor; agent
training and testing; agent commission
structure and plan oversight of agents.
Data collected via Medicare Part C
Reporting Requirements will be an
integral resource for oversight,
E:\FR\FM\03OCN1.SGM
03OCN1
mstockstill on PROD1PC66 with NOTICES
57632
Federal Register / Vol. 73, No. 193 / Friday, October 3, 2008 / Notices
monitoring, compliance and auditing
activities necessary to ensure quality
provision of the benefits provided by
MA plans to enrollees. Refer to the
‘‘Summary of Revisions’’ document for
a list of the recent collection changes.
Form Number: CMS–10261 (OMB#
0938–New); Frequency: Yearly,
Quarterly, and Semi-annually; Affected
Public: Business or other for-profits;
Number of Respondents: 718; Total
Annual Responses: 12,709; Total
Annual Hours: 286,944.
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:
VerDate Aug<31>2005
23:33 Oct 02, 2008
Jkt 217001
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: Payment Error
Rate Measurement in Medicaid and the
State Children 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 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.
4.Type of Information Collection
Request: Extension without change of a
currently approved collection; Title of
Information Collection: Collection of
Drug Pricing and Network Pharmacy
Data from Medicare Prescription Drug
Plans (PDPs and MA–PDs) and
Supporting Regulations in 42 CFR
423.48; Use: Both stand alone
prescription drug plans (PDPs) and
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
Medicare Advantage Prescription Drug
(MA–PDs) plans are required to submit
drug pricing and pharmacy network
data to CMS and these data are made
publicly available to people with
Medicare through the Medicare
Prescription Drug Plan Finder Web tool
on https://www.medicare.gov. Drug
prices vary across a plans pharmacy
network based on the contracts that
each plan negotiates with each
pharmacy or pharmacy chain in their
networks. The pharmacy networks can
change during the course of the year as
new pharmacies open, close, change
ownership, or plans negotiate new
contracts with pharmacies resulting in
different dispensing fees for
prescriptions. Drug prices also change
frequently due to the daily fluctuation
of the Average Wholesale Price (AWP),
thus plans increase or decrease their
drug prices to reflect these changes. The
purpose of the data is to enable
prospective and current Medicare
beneficiaries to compare, learn, select
and enroll in a plan that best meets their
needs. The database structure provides
the necessary drug pricing and
pharmacy network information to
accurately communicate plan
information in a comparative format.
Form Number: CMS–10150 (OMB#
0938–0951); Frequency: Bi-weekly;
Affected Public: Business or other forprofits; Number of Respondents: 680;
Total Annual Responses: 17,680; Total
Annual Hours: 70,720.
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 by the OMB desk officer at
the address below, no later than 5 p.m.
onNovember 3, 2008.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS Desk
Officer, New Executive Office Building,
Room 10235, Washington, DC 20503,
Fax Number: (202) 395–6974.
Dated: September 26, 2008.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E8–23415 Filed 10–2–08; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\03OCN1.SGM
03OCN1
Agencies
[Federal Register Volume 73, Number 193 (Friday, October 3, 2008)]
[Notices]
[Pages 57631-57632]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-23415]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10261, CMS-10182, CMS-10166 and CMS-10150]
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: New collection; Title of
Information Collection: Part C Medicare Advantage (MA) Reporting
Requirements and Supporting Regulations in 42 CFR 422.516 (a); Use: CMS
has authority to establish reporting requirements for Medicare
Advantage Organizations (MAOs) as described in 42 CFR 422.516(a). Under
that authority, each MAO must have an effective procedure to develop,
compile, evaluate, and report to CMS, to its enrollees, and to the
general public, at the times and in the manner that CMS requires, and
while safeguarding the confidentiality of the doctor-patient
relationship, statistics and other information with respect to the cost
of its operations, patterns of service utilization, availability,
accessibility, and acceptability of its services, developments in the
health status of its enrollees, and other matters that CMS may require.
CMS will not require cost plans to comply with the following
reporting requirements: Benefit utilization; procedure frequency; and
serious reportable adverse events. However, CMS has determined that it
is essential that all beneficiaries understand rules and requirements
of the Medicare plans which they are being invited to join. Prospective
enrollees in cost plans should be furnished accurate information by
qualified sales people, consistent with CMS' expectation for
prospective enrollees in other play types. Thus, CMS is requiring
reporting on certain measures CMS' believes is critical in monitoring
cost plans. Additionally, CMS believes that section 1876(i)(1)(D) of
the Act, and 42 CFR 417.126(a)(6) permits CMS to require cost plans to
report to CMS the data identified as follows: Provider network
adequacy; grievances; organization determinations/reconsiderations;
employer group plan sponsor; agent training and testing; agent
commission structure and plan oversight of agents.
Data collected via Medicare Part C Reporting Requirements will be
an integral resource for oversight,
[[Page 57632]]
monitoring, compliance and auditing activities necessary to ensure
quality provision of the benefits provided by MA plans to enrollees.
Refer to the ``Summary of Revisions'' document for a list of the recent
collection changes. Form Number: CMS-10261 (OMB 0938-New);
Frequency: Yearly, Quarterly, and Semi-annually; Affected Public:
Business or other for-profits; Number of Respondents: 718; Total Annual
Responses: 12,709; Total Annual Hours: 286,944.
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: Payment Error
Rate Measurement in Medicaid and the State Children 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 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.
4.Type of Information Collection Request: Extension without change
of a currently approved collection; Title of Information Collection:
Collection of Drug Pricing and Network Pharmacy Data from Medicare
Prescription Drug Plans (PDPs and MA-PDs) and Supporting Regulations in
42 CFR 423.48; Use: Both stand alone prescription drug plans (PDPs) and
Medicare Advantage Prescription Drug (MA-PDs) plans are required to
submit drug pricing and pharmacy network data to CMS and these data are
made publicly available to people with Medicare through the Medicare
Prescription Drug Plan Finder Web tool on https://www.medicare.gov. Drug
prices vary across a plans pharmacy network based on the contracts that
each plan negotiates with each pharmacy or pharmacy chain in their
networks. The pharmacy networks can change during the course of the
year as new pharmacies open, close, change ownership, or plans
negotiate new contracts with pharmacies resulting in different
dispensing fees for prescriptions. Drug prices also change frequently
due to the daily fluctuation of the Average Wholesale Price (AWP), thus
plans increase or decrease their drug prices to reflect these changes.
The purpose of the data is to enable prospective and current Medicare
beneficiaries to compare, learn, select and enroll in a plan that best
meets their needs. The database structure provides the necessary drug
pricing and pharmacy network information to accurately communicate plan
information in a comparative format. Form Number: CMS-10150
(OMB 0938-0951); Frequency: Bi-weekly; Affected Public:
Business or other for-profits; Number of Respondents: 680; Total Annual
Responses: 17,680; Total Annual Hours: 70,720.
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 by the OMB desk
officer at the address below, no later than 5 p.m. onNovember 3, 2008.
OMB, Office of Information and Regulatory Affairs, Attention: CMS
Desk Officer, New Executive Office Building, Room 10235, Washington, DC
20503, Fax Number: (202) 395-6974.
Dated: September 26, 2008.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E8-23415 Filed 10-2-08; 8:45 am]
BILLING CODE 4120-01-P