Office of the National Coordinator for Health Information Technology; Notice of Public Meeting, 48644-48645 [07-4151]
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Federal Register / Vol. 72, No. 164 / Friday, August 24, 2007 / Notices
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Misys Hospital Systems, Inc.
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By Direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 07–4150 Filed 8–23–07; 8:45 am]
BILLING CODE 6750–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology; Notice
of Public Meeting
Notice of intent to hold a public
meeting to share information on
establishing an American Health
Information Community Successor.
yshivers on PROD1PC66 with NOTICES
ACTION:
SUMMARY: On September 5, 2007, the
Office of the National Coordinator for
Health Information Technology will
lead a technical assistance public
meeting to share information and
VerDate Aug<31>2005
16:49 Aug 23, 2007
Jkt 211001
VoiceSignal Technologies, Inc. ...
David
Martin
and
Nancy
Knowlton.
McDonald’s Corporation ..............
Apple Inc. .....................................
VoiceSignal Technologies, Inc.
1329169 Alberta Ltd.
Boston Market Corporation.
Apple Inc.
answer detailed questions about plans
to design and establish a successor to
the American Health Information
community, including information on
the Notice of Funding Availability.
The AHIC is a federally chartered
advisory committee that provides input
and recommendations to the
Department of Health and Human
Services (HHS) on how to make health
records digital and interoperable, and
how to assure that the privacy and
security of those records are protected.
(Please visit https://www.hhs.gov/
healthit/community/background/ for
more information on the AHIC.) The
AHIC charter specifies that the AHIC
will develop and advance
recommendations to the Secretary on a
private-sector health information
community initiative that will succeed
the AHIC. The AHIC successor will
bring together public and private, notfor-profit and for-profit entities that
represent all sectors of the health
community. This new public-private
partnership will develop a unified
approach to realize an effective, secure,
interoperable nationwide health
information system that improves the
quality, safety, and efficiency of health
care in the U.S. For the purposes of
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Fmt 4703
Sfmt 4703
facilitating the establishment of the
AHIC successor and convening a
planning board, HHS will award a
Cooperative Agreement that allows for
substantial involvement by the Federal
government. Once a new legal entity is
established and after certain conditions
are met, HHS will support that entity
through additional funding that will
enable initial operations and transition
of specific AHIC responsibilities by late
Fall 2008.
September 5, 2007, from 9:30
a.m. to 12 p.m. (EDT); registration opens
at 9 a.m.
DATES:
Hubert H. Humphrey
building (200 Independence Avenue,
SW., Washington, DC 20201),
Conference Room 705A.
A link to the Web cast of the public
meeting will be available on the AHIC
transition Web site at: https://
www.hhs.gov/healthit/community/
background/AHICsuccessor.html.
Instructions will be available on the
day of the meeting about how to submit
questions or comments via phone or email.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
https://www.hhs.gov/healthit/
E:\FR\FM\24AUN1.SGM
24AUN1
Visit
Federal Register / Vol. 72, No. 164 / Friday, August 24, 2007 / Notices
community/background/
AHICsuccessor.html.
Dated: August 20, 2007.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. 07–4151 Filed 8–23–07; 8:45 am]
BILLING CODE 4150–24–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10241, CMS–
382, CMS–10247, and CMS–10246]
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: New Collection.
Title of Information Collection:
Annual State Report and Annual State
Performance Rankings.
Use: The Deficit Reduction Act of
2005 (DRA) requires CMS to contract
with a vendor to conduct a monthly
national survey of retail prescription
drug prices and to report the prices to
the States. These national average prices
will be used as a benchmark by the
States for the management of their
prescription drug programs. The law
also requires that States report their
drug utilization rates for noninnovator
multiple source drugs, their payment
rates under their State plan, and their
dispensing fees. A template will be used
yshivers on PROD1PC66 with NOTICES
AGENCY:
VerDate Aug<31>2005
14:35 Aug 23, 2007
Jkt 211001
to facilitate data collection. The States’
rankings are to be presented to the
Congress and the States.
Form Number: CMS–10241 (OMB#:
0938–NEW).
Frequency: Reporting—Yearly.
Affected Public: States, Local or Tribal
Governments.
Number of Respondents: 51.
Total Annual Responses: 51.
Total Annual Hours: 765.
2. Type of Information Collection
Request: Extension without change of a
currently approved collection.
Title of Information Collection: ESRD
Beneficiary Selection and Supporting
Regulations Contained in 42 CFR
414.330.
Use: Section 2145 amended section
1881 of the Social Security Act and
changes the way the Medicare program
pays for home dialysis services.
Medicare patients who currently receive
dialysis in a facility but later become
home dialysis patients must complete
the CMS–382 form at the time they go
to the home setting. Facilities are
required to have all Medicare home
dialysis patients choose one of two
payment methods. Under Method I, the
dialysis facility assumes responsibility
for patient care and the facility provides
all dialysis equipment and supplies
needed to dialyze at home. The facility
is required to order, store, deliver, and
pay the manufacturers and suppliers for
these items. Under Method II, the
beneficiary makes his/her own
arrangement for securing the necessary
supplies and dialysis equipment. Then,
the supplier bills the Medicare program
(Carrier) for payment.
Form Number: CMS–382 (OMB#:
0938–0372).
Frequency: Reporting—Yearly.
Affected Public: Individuals or
households.
Number of Respondents: 7400.
Total Annual Responses: 7400.
Total Annual Hours: 617.
3. Type of Information Collection
Request: New collection.
Title of Information Collection:
Sponsor application for CMS coverage
under the Medicare Clinical Trial
Research Policy.
Use: The Centers for Medicare &
Medicaid Services (CMS) has supported
the participation of beneficiaries in
clinical research through its Clinical
Trial Policy implemented through the
National coverage determination (NCD)
process since 2000. Support for
participation in clinical research studies
is provided through the coverage of
items and services that are considered
usual patient care. Usual patient care
encompasses all items and services
covered by the program for any
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48645
beneficiary, i.e., reasonable and
necessary for the diagnosis or treatment
of illness or injury to improve the
functioning of a malformed body
member.
In accordance with the Clinical Trial
Policy/Clinical Research Policy (CTP/
CRP), CMS requires study sponsors/
principal investigators to meet a set of
standards to (1) Ensure that all sponsors
and investigators conduct clinical
research so that Medicare covered items
and services are reasonable and
necessary to obtain valid research
outcomes and for treating research
participants, and (2) maximize the
health outcomes (and minimize risk) for
Medicare beneficiaries.
One of the standards states, ‘‘The
clinical research study is registered on
the ClinicalTrials.gov Web site by the
study sponsor/principal investigator
prior to the enrollment of the first study
subject.’’ In practice, we anticipate that
study sponsors/principal investigators
wishing to have their research study
listed as certified on our Web site, and
in the Federal Register will register the
study on ClinicalTrials.gov and
complete a form to CMS describing the
scope and nature of the clinical
research, discussing each of the
standards in this policy, and certifying
that all standards in this policy have
been met. CMS will only review this
form for completeness. We are seeking
OMB approval for the form.
Form Number: CMS–10247 (OMB#:
0938–New).
Frequency: Reporting—one-time.
Affected Public: Private Sector—
Business or other for-profits and not-forprofit institutions.
Number of Respondents: 4,524.
Total Annual Responses: 4,524.
Total Annual Hours: 4,524.
4. Type of Information Collection
Request: New collection.
Title of Information Collection: Cost
and Resource Utilization (CRU) Data
Collection for the Medicare Post Acute
Care Payment Reform Demonstration.
Use: The CRU data collection is part
of the Post-Acute Care Payment Reform
Demonstration mandated by Section
5008 of the Deficit Reduction Act of
2005. This demonstration is intended to
address problems with the current
Medicare payment systems for postacute care services, including those for
Long Term Care Hospitals, Inpatient
Rehabilitation Facilities, Skilled
Nursing Facilities, and Home Health
Agencies. Each of these four types of
providers currently has a separate
prospective payment system (PPS) with
its own case-mix groups, payment units,
and rates. Each case-mix grouper uses a
unique set of items to measure patients,
E:\FR\FM\24AUN1.SGM
24AUN1
Agencies
[Federal Register Volume 72, Number 164 (Friday, August 24, 2007)]
[Notices]
[Pages 48644-48645]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 07-4151]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the National Coordinator for Health Information
Technology; Notice of Public Meeting
ACTION: Notice of intent to hold a public meeting to share information
on establishing an American Health Information Community Successor.
-----------------------------------------------------------------------
SUMMARY: On September 5, 2007, the Office of the National Coordinator
for Health Information Technology will lead a technical assistance
public meeting to share information and answer detailed questions about
plans to design and establish a successor to the American Health
Information community, including information on the Notice of Funding
Availability.
The AHIC is a federally chartered advisory committee that provides
input and recommendations to the Department of Health and Human
Services (HHS) on how to make health records digital and interoperable,
and how to assure that the privacy and security of those records are
protected. (Please visit https://www.hhs.gov/healthit/community/
background/ for more information on the AHIC.) The AHIC charter
specifies that the AHIC will develop and advance recommendations to the
Secretary on a private-sector health information community initiative
that will succeed the AHIC. The AHIC successor will bring together
public and private, not-for-profit and for-profit entities that
represent all sectors of the health community. This new public-private
partnership will develop a unified approach to realize an effective,
secure, interoperable nationwide health information system that
improves the quality, safety, and efficiency of health care in the U.S.
For the purposes of facilitating the establishment of the AHIC
successor and convening a planning board, HHS will award a Cooperative
Agreement that allows for substantial involvement by the Federal
government. Once a new legal entity is established and after certain
conditions are met, HHS will support that entity through additional
funding that will enable initial operations and transition of specific
AHIC responsibilities by late Fall 2008.
DATES: September 5, 2007, from 9:30 a.m. to 12 p.m. (EDT); registration
opens at 9 a.m.
ADDRESSES: Hubert H. Humphrey building (200 Independence Avenue, SW.,
Washington, DC 20201), Conference Room 705A.
A link to the Web cast of the public meeting will be available on
the AHIC transition Web site at: https://www.hhs.gov/healthit/community/
background/AHICsuccessor.html.
Instructions will be available on the day of the meeting about how
to submit questions or comments via phone or e-mail.
FOR FURTHER INFORMATION CONTACT: Visit https://www.hhs.gov/healthit/
[[Page 48645]]
community/background/AHICsuccessor.html.
Dated: August 20, 2007.
Judith Sparrow,
Director, American Health Information Community, Office of Programs and
Coordination, Office of the National Coordinator for Health Information
Technology.
[FR Doc. 07-4151 Filed 8-23-07; 8:45 am]
BILLING CODE 4150-24-M