Agency Information Collection Activities: Submission for OMB Review; Comment Request, 8877-8878 [E8-2804]
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8877
Federal Register / Vol. 73, No. 32 / Friday, February 15, 2008 / Notices
then send reports to CDC using deidentified data. It is from these reports
that CDC is able to determine funding
levels.
In addition to reporting child blood
lead levels, many laboratories also
report adult blood lead levels. Thus, this
OMB request would also like to include
the Adult Blood Lead Epidemiology and
Surveillance Program (ABLES). The
ABLES Program is a state-based
surveillance system under which
participating States provide information
to CDC’s National Institute for
Occupational Safety and Health
(NIOSH) on laboratory reported blood
lead levels among adults. For all adults
(16 and older) the State will provide
data on all laboratory reports when the
adult’s blood lead level is equal to or
greater than 25 mcg/dl. These data are
to be consolidated into a single data
submission by task time periods.
The ABLES program ultimately aims
to collect the complete list of variables
for all blood lead tests, including blood
lead levels less than 25 mcg/dl, and
urges all States to progressively supply
this information as it becomes available.
All data submissions must be delivered
in the supplied format providing a field
for 20 variables, even if some variables
have no data available at the time.
The use of both Childhood Lead
Surveillance System and the ABLES
Program will allow us to systematically
track pockets of exposure to lead. It will
also allow us to fully understand
exposure potential and ways in which
to prevent future sources of lead
poisoning. Both systems are invaluable
and will no doubt help us as we
continue our stride in the elimination of
lead poisoning in our nation.
There is no cost to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
response per
respondent
Number of
respondents
Respondents
Average
burden per
response
(in hrs.)
Total burden
hours
State and Local Health Departments for Child Surveillance ...........................
State and Local Health Departments for Adult Surveillance ...........................
42
40
4
4
2
2
336
320
Total ..........................................................................................................
........................
........................
........................
656
Dated: February 6, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–2836 Filed 2–14–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10242, CMS–
10165, CMS–10251, CMS–R–218 and CMS–
10252]
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
rwilkins on PROD1PC63 with NOTICES
AGENCY:
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15:58 Feb 14, 2008
Jkt 214001
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: Revisions to
Payment Policies Under the Physician
Fee Schedule, Other Changes to
Payment Under Part B, and Revisions to
Payment Policies for Ambulance
Services for CY 2008 (42 CFR 424.36—
Signature Requirements); Use: Section
42 CFR 424.33(a)(3) states that all claims
must be signed by the beneficiary or the
beneficiary’s representative (in
accordance with 42 CFR 424.36(b)).
Section 42 CFR 424.36(a) states that the
beneficiary’s signature is required on a
claim unless the beneficiary has died or
the provisions of 424.36(b), (c), or (d)
apply. The statutory authority requiring
a beneficiary’s signature on a claim
submitted by a provider is located in
section 1835(a) and in 1814(a) of the
Social Security Act (the Act), for Part B
and Part A services, respectively. The
authority requiring a beneficiary’s
signature for supplier claims is implicit
in sections 1842(b)(3)(B)(ii) and in
1848(g)(4) of the Act. Because it is very
difficult to obtain a beneficiary’s
signature (or the signature of a person
authorized to sign on behalf of the
beneficiary) on a claim when the
beneficiary is being transported by
ambulance in emergency situations,
PO 00000
Frm 00034
Fmt 4703
Sfmt 4703
CMS is proposing that, for emergency
ambulance transport services, an
ambulance provider or supplier may
submit the claim without a beneficiary’s
signature, as long as certain
documentation requirements are met.
The information collected will be used
by CMS contractors (both, fiscal
intermediaries and carriers) that process
and pay emergency ambulance transport
claims. Form Number: CMS–10242
(OMB#: 0938–New); Frequency:
Reporting: Hourly, Daily, Weekly,
Monthly and Yearly; Affected Public:
Business or other for-profit and Not-forprofit institutions; Number of
Respondents: 9,000; Total Annual
Responses: 6,500,000; Total Annual
Hours: 541,667.
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Electronic
Health Record; Use: The purpose of this
demonstration project is to reward the
delivery of high-quality care supported
by the adoption and use of electronic
health records in small to medium-sized
primary care physician practices. While
this is separate and distinct from the
Medicare Care Management
Performance (MCMP) Demonstration, it
expands upon the foundation created by
the MCMP Demonstration, which was
mandated by Section 649 of the
Medicare Prescription Drug,
Improvement and Modernization Act of
2003. The electronic health record
demonstration will be operational for a
5-year period and will be operated
E:\FR\FM\15FEN1.SGM
15FEN1
rwilkins on PROD1PC63 with NOTICES
8878
Federal Register / Vol. 73, No. 32 / Friday, February 15, 2008 / Notices
under section 402 demonstration waiver
authority. The information to be
obtained as part of the application form
is necessary to document basic
information for physician practices that
intend to participate in this
demonstration initiative. Form Number:
CMS–10165 (OMB#: 0938–0965);
Frequency: Once; Affected Public:
Private sector—Business or other forprofit; Number of Respondents: 2400;
Total Annual Responses: 2400; Total
Annual Hours: 520.
3. Type of Information Collection
Request: New Collection; Title of
Information Collection: State Plan Preprint for Integrated Medicare and
Medicaid Programs; Use: Information
submitted via the State Plan
Amendment (SPA) pre-print will be
used by CMS Central and Regional
Offices to analyze a State’s proposal to
implement integrated Medicare and
Medicaid programs. The pre-print is an
optional document for use by States to
highlight the arrangements between a
State and Medicare Advantage Special
Needs Plans that are also providing
Medicaid services. State Medicaid
Agencies will complete the SPA preprint and submit it to CMS for a
comprehensive analysis. The pre-print
provides the opportunity for States to
confirm that their integrated care model
complies with both Federal statutory
and regulatory requirements. The preprint contains assurances, check-off
items, and areas for States to describe
policies and procedures for subjects
such as enrollment, marketing and
quality assurance. Based on comments
received during the 60-day comment
period, both the instructions and preprint have been revised. Form Numbers:
CMS–10251 (OMB#: 0938–NEW);
Frequency: Reporting—Once; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 30; Total
Annual Hours: 600.
4. Type of Information Collection
Request: Extension of currently
approved collection; Title of
Information Collection: Information
Collection Requirements Contained in
45 CFR Part 162; HIPAA Standards for
Electronic Transactions; Use: This
submission contains information
collection requirements in HCFA–0149–
F, CMS–0003–P, CMS–0005–P, and
CMS–003/005–F. This collection
establishes standards for electronic
transactions and for code sets to be used
in those transactions. The collection
standardizes the approximately 400
formats of electronic health care claims
used in the United States. The use of
these standards significantly reduces the
administrative burden associated with
VerDate Aug<31>2005
15:58 Feb 14, 2008
Jkt 214001
paper documents, lowers operating
costs, and improves data quality for
health care providers and health plans;
Form Number: CMS–R–218 (OMB#
0938–0866); Frequency: On occasion;
Affected Public: Business or other forprofit; Number of Respondents:
3,400,000; Total Annual Responses:
3,400,000; Total Annual Hours: 1.
5. Type of Information Collection
Request: New collection; Title of
Information Collection: Certificate of
Destruction for Data Acquired from the
Centers for Medicare and Medicaid
Services; Use: The Certificate of
Destruction will be used by recipients of
CMS data to certify that they have
destroyed the data they have received
through a CMS Data Use Agreement
(DUA). The DUA requires the
destruction of the data at the completion
of the project/expiration of the DUA.
The DUA addresses the conditions
under which CMS will disclose and the
User will maintain CMS data that are
protected by the Privacy Act of 1974,
§ 552a and the Health Insurance
Portability Accountability Act of 1996.
CMS has developed policies and
procedures for such disclosures that are
based on the Privacy Act and the Health
Insurance Portability Act (HIPAA). The
Certificate of Destruction is required to
close out the DUA and to ensure the
data are destroyed and not used for
another purpose. Form Number: CMS–
10252 (OMB# 0938-New); Frequency:
On occasion; Affected Public: Business
or other for-profit; Number of
Respondents: 500; Total Annual
Responses: 500; Total Annual Hours:
84.
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.
on March 17, 2008.
OMB Human Resources and Housing
Branch, Attention: Carolyn Lovett, New
Executive Office Building, Room 10235,
Washington, DC 20503, Fax Number:
(202) 395–6974.
PO 00000
Frm 00035
Fmt 4703
Sfmt 4703
Dated: February 8, 2008.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E8–2804 Filed 2–14–08; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–267]
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
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: Medicare
Advantage Program Requirements
Referenced in 42 CFR part 422; Use: The
information collection requirements are
mandated by 42 CFR part 422. Section
4001 of the Balanced Budget Act of 1997
(BBA) added sections 1851 through
1859 to the Social Security Act to
establish this program. The Medicare,
Medicaid, and SCHIP Benefits
Improvement Act and Protection Act of
2000, also added new requirements in
addition to the Medicare Prescription
Drug, Improvement, and Modernization
Act of 2003.
Medicare Advantage (MA)
organizations (formerly M+C
organizations) and potential MA
organizations (applicants) use the
information discussed to comply with
the eligibility requirements and the MA
AGENCY:
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Agencies
[Federal Register Volume 73, Number 32 (Friday, February 15, 2008)]
[Notices]
[Pages 8877-8878]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-2804]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10242, CMS-10165, CMS-10251, CMS-R-218 and
CMS-10252]
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: Revisions to Payment Policies Under the
Physician Fee Schedule, Other Changes to Payment Under Part B, and
Revisions to Payment Policies for Ambulance Services for CY 2008 (42
CFR 424.36--Signature Requirements); Use: Section 42 CFR 424.33(a)(3)
states that all claims must be signed by the beneficiary or the
beneficiary's representative (in accordance with 42 CFR 424.36(b)).
Section 42 CFR 424.36(a) states that the beneficiary's signature is
required on a claim unless the beneficiary has died or the provisions
of 424.36(b), (c), or (d) apply. The statutory authority requiring a
beneficiary's signature on a claim submitted by a provider is located
in section 1835(a) and in 1814(a) of the Social Security Act (the Act),
for Part B and Part A services, respectively. The authority requiring a
beneficiary's signature for supplier claims is implicit in sections
1842(b)(3)(B)(ii) and in 1848(g)(4) of the Act. Because it is very
difficult to obtain a beneficiary's signature (or the signature of a
person authorized to sign on behalf of the beneficiary) on a claim when
the beneficiary is being transported by ambulance in emergency
situations, CMS is proposing that, for emergency ambulance transport
services, an ambulance provider or supplier may submit the claim
without a beneficiary's signature, as long as certain documentation
requirements are met. The information collected will be used by CMS
contractors (both, fiscal intermediaries and carriers) that process and
pay emergency ambulance transport claims. Form Number: CMS-10242
(OMB: 0938-New); Frequency: Reporting: Hourly, Daily, Weekly,
Monthly and Yearly; Affected Public: Business or other for-profit and
Not-for-profit institutions; Number of Respondents: 9,000; Total Annual
Responses: 6,500,000; Total Annual Hours: 541,667.
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Electronic Health
Record; Use: The purpose of this demonstration project is to reward the
delivery of high-quality care supported by the adoption and use of
electronic health records in small to medium-sized primary care
physician practices. While this is separate and distinct from the
Medicare Care Management Performance (MCMP) Demonstration, it expands
upon the foundation created by the MCMP Demonstration, which was
mandated by Section 649 of the Medicare Prescription Drug, Improvement
and Modernization Act of 2003. The electronic health record
demonstration will be operational for a 5-year period and will be
operated
[[Page 8878]]
under section 402 demonstration waiver authority. The information to be
obtained as part of the application form is necessary to document basic
information for physician practices that intend to participate in this
demonstration initiative. Form Number: CMS-10165 (OMB: 0938-
0965); Frequency: Once; Affected Public: Private sector--Business or
other for-profit; Number of Respondents: 2400; Total Annual Responses:
2400; Total Annual Hours: 520.
3. Type of Information Collection Request: New Collection; Title of
Information Collection: State Plan Pre-print for Integrated Medicare
and Medicaid Programs; Use: Information submitted via the State Plan
Amendment (SPA) pre-print will be used by CMS Central and Regional
Offices to analyze a State's proposal to implement integrated Medicare
and Medicaid programs. The pre-print is an optional document for use by
States to highlight the arrangements between a State and Medicare
Advantage Special Needs Plans that are also providing Medicaid
services. State Medicaid Agencies will complete the SPA pre-print and
submit it to CMS for a comprehensive analysis. The pre-print provides
the opportunity for States to confirm that their integrated care model
complies with both Federal statutory and regulatory requirements. The
pre-print contains assurances, check-off items, and areas for States to
describe policies and procedures for subjects such as enrollment,
marketing and quality assurance. Based on comments received during the
60-day comment period, both the instructions and pre-print have been
revised. Form Numbers: CMS-10251 (OMB: 0938-NEW); Frequency:
Reporting--Once; Affected Public: State, Local, or Tribal Governments;
Number of Respondents: 56; Total Annual Responses: 30; Total Annual
Hours: 600.
4. Type of Information Collection Request: Extension of currently
approved collection; Title of Information Collection: Information
Collection Requirements Contained in 45 CFR Part 162; HIPAA Standards
for Electronic Transactions; Use: This submission contains information
collection requirements in HCFA-0149-F, CMS-0003-P, CMS-0005-P, and
CMS-003/005-F. This collection establishes standards for electronic
transactions and for code sets to be used in those transactions. The
collection standardizes the approximately 400 formats of electronic
health care claims used in the United States. The use of these
standards significantly reduces the administrative burden associated
with paper documents, lowers operating costs, and improves data quality
for health care providers and health plans; Form Number: CMS-R-218
(OMB 0938-0866); Frequency: On occasion; Affected Public:
Business or other for-profit; Number of Respondents: 3,400,000; Total
Annual Responses: 3,400,000; Total Annual Hours: 1.
5. Type of Information Collection Request: New collection; Title of
Information Collection: Certificate of Destruction for Data Acquired
from the Centers for Medicare and Medicaid Services; Use: The
Certificate of Destruction will be used by recipients of CMS data to
certify that they have destroyed the data they have received through a
CMS Data Use Agreement (DUA). The DUA requires the destruction of the
data at the completion of the project/expiration of the DUA. The DUA
addresses the conditions under which CMS will disclose and the User
will maintain CMS data that are protected by the Privacy Act of 1974,
Sec. 552a and the Health Insurance Portability Accountability Act of
1996. CMS has developed policies and procedures for such disclosures
that are based on the Privacy Act and the Health Insurance Portability
Act (HIPAA). The Certificate of Destruction is required to close out
the DUA and to ensure the data are destroyed and not used for another
purpose. Form Number: CMS-10252 (OMB 0938-New); Frequency: On
occasion; Affected Public: Business or other for-profit; Number of
Respondents: 500; Total Annual Responses: 500; Total Annual Hours: 84.
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. on March 17, 2008.
OMB Human Resources and Housing Branch, Attention: Carolyn Lovett,
New Executive Office Building, Room 10235, Washington, DC 20503, Fax
Number: (202) 395-6974.
Dated: February 8, 2008.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E8-2804 Filed 2-14-08; 8:45 am]
BILLING CODE 4120-01-P