Agency Information Collection Activities: Proposed Collection; Comment Request, 26819 [E7-9079]
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Federal Register / Vol. 72, No. 91 / Friday, May 11, 2007 / Notices
Federal Advisory Committee Act (Pub.
L. 92–463, 5 U.S.C., App.).
DATES: June 15, 2007, from 10 a.m. to
3:30 p.m. [Eastern time].
ADDRESSES: Hubert H. Humphrey
Building (200 Independence Avenue,
SW., Washington, DC 20201),
Conference Room 705A (please bring
photo ID for entry to a Federal building).
FOR FURTHER INFORMATION CONTACT:
https://www.hhs.gov/healthit/ahic/
population/.
SUPPLEMENTARY INFORMATION: The
Workgroup will continue its discussion
on how to facilitate the flow of reliable
health information among population
health and clinical care systems
necessary to protect and improve the
public’s health. This meeting will focus
on countermeasure allocation,
distribution and administration, as well
as automated integration with response
registries.
The meeting will be available via Web
cast. For additional information, go to:
https://www.hhs.gov/healthit/ahic/
population/pop_instruct.html.
Dated: May 3, 2007.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. 07–2328 Filed 5–10–07; 8:45 am]
BILLING CODE 4150–24–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–855]
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,
ycherry on PROD1PC64 with NOTICES
AGENCY:
VerDate Aug<31>2005
21:09 May 10, 2007
Jkt 211001
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
Enrollment Application; Form Number:
CMS–855 (OMB#: 0938–0685); Use: The
primary function of the Medicare
enrollment application is to gather
information from a provider or supplier
that tells us who it is, whether it meets
certain qualifications to be a health care
provider or supplier, where it practices
or renders its services, the identity of
the owners of the enrolling entity, and
information necessary to establish the
correct claims payment. The goal of
evaluating and revising the Medicare
enrollment applications is to simplify
and clarify the information collection
without jeopardizing our need to collect
specific information.
We are proposing revisions to the
CMS–855B to incorporate changes
adopted in CMS–1321–FC (71 FR
69624), ‘‘Revisions to Payment Policies
and Five-Year Review of Relative Value
Units Under the Physician Fee Schedule
for CY 2007 and Other Changes to
Payment Under Part B; Revisions to
Ambulance Fee Schedule; Ambulatory
Inflation Factor Update for CY 2007.’’
Specifically, CMS is revising the CMS–
855B to:
• Add instructions to Attachment 2
that explain the independent diagnostic
testing facility (IDTF) liability insurance
requirements in 42 CFR 410.33(g)(6).
• Require that an IDTF submit copies
of its comprehensive liability insurance
policy in Section 17.
• List all of the new IDTF standards
on a separate page in Attachment 2.
• Remove the supplier type
‘‘Voluntary Health/Charitable Agency’’
from Section 2A.
In addition, we are trying to enhance
our ability to identify whether a hospital
qualifies as a ‘‘specialty hospital.’’ To
this end, we propose to revise the CMS–
855A to include a specific box that
specialty hospitals must check when
completing the application. Instructions
explaining the definition of a ‘‘specialty
hospital’’ will also be added to the form.
We also provide clarification of the term
‘‘primary practice location’’ in the
instructions in Section 4 of the CMS–
855A. This clarification does not change
any data elements on the form. We are
also removing the data element
‘‘Medicare Year-End Cost Report Date’’
in Section 2 of the CMS–855A, as this
information is no longer needed.
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26819
Frequency: Recordkeeping and
Reporting—On occasion; Affected
Public: Business or other for-profit and
Not-for-profit institutions; Number of
Respondents: 400,000; Total Annual
Responses: 400,000; Total Annual
Hours: 1,001,503.33.
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 10, 2007.
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 3, 2007.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E7–9079 Filed 5–10–07; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Substance Abuse and Mental Health
Services Administration
Current List of Laboratories Which
Meet Minimum Standards To Engage in
Urine Drug Testing for Federal
Agencies
Substance Abuse and Mental
Health Services Administration, HHS.
ACTION: Notice.
AGENCY:
SUMMARY: The Department of Health and
Human Services (HHS) notifies Federal
agencies of the laboratories currently
certified to meet the standards of
Subpart C of the Mandatory Guidelines
for Federal Workplace Drug Testing
Programs (Mandatory Guidelines). The
Mandatory Guidelines were first
published in the Federal Register on
April 11, 1988 (53 FR 11970), and
subsequently revised in the Federal
Register on June 9, 1994 (59 FR 29908),
on September 30, 1997 (62 FR 51118),
and on April 13, 2004 (69 FR 19644).
E:\FR\FM\11MYN1.SGM
11MYN1
Agencies
[Federal Register Volume 72, Number 91 (Friday, May 11, 2007)]
[Notices]
[Page 26819]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-9079]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-855]
Agency Information Collection Activities: Proposed Collection;
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) 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
Enrollment Application; Form Number: CMS-855 (OMB: 0938-0685);
Use: The primary function of the Medicare enrollment application is to
gather information from a provider or supplier that tells us who it is,
whether it meets certain qualifications to be a health care provider or
supplier, where it practices or renders its services, the identity of
the owners of the enrolling entity, and information necessary to
establish the correct claims payment. The goal of evaluating and
revising the Medicare enrollment applications is to simplify and
clarify the information collection without jeopardizing our need to
collect specific information.
We are proposing revisions to the CMS-855B to incorporate changes
adopted in CMS-1321-FC (71 FR 69624), ``Revisions to Payment Policies
and Five-Year Review of Relative Value Units Under the Physician Fee
Schedule for CY 2007 and Other Changes to Payment Under Part B;
Revisions to Ambulance Fee Schedule; Ambulatory Inflation Factor Update
for CY 2007.'' Specifically, CMS is revising the CMS-855B to:
Add instructions to Attachment 2 that explain the
independent diagnostic testing facility (IDTF) liability insurance
requirements in 42 CFR 410.33(g)(6).
Require that an IDTF submit copies of its comprehensive
liability insurance policy in Section 17.
List all of the new IDTF standards on a separate page in
Attachment 2.
Remove the supplier type ``Voluntary Health/Charitable
Agency'' from Section 2A.
In addition, we are trying to enhance our ability to identify
whether a hospital qualifies as a ``specialty hospital.'' To this end,
we propose to revise the CMS-855A to include a specific box that
specialty hospitals must check when completing the application.
Instructions explaining the definition of a ``specialty hospital'' will
also be added to the form. We also provide clarification of the term
``primary practice location'' in the instructions in Section 4 of the
CMS-855A. This clarification does not change any data elements on the
form. We are also removing the data element ``Medicare Year-End Cost
Report Date'' in Section 2 of the CMS-855A, as this information is no
longer needed. Frequency: Recordkeeping and Reporting--On occasion;
Affected Public: Business or other for-profit and Not-for-profit
institutions; Number of Respondents: 400,000; Total Annual Responses:
400,000; Total Annual Hours: 1,001,503.33.
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 10, 2007.
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 3, 2007.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E7-9079 Filed 5-10-07; 8:45 am]
BILLING CODE 4120-01-P