Agency Information Collection Activities: Proposed Collection; Comment Request, 4202-4203 [E9-1435]
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Federal Register / Vol. 74, No. 14 / Friday, January 23, 2009 / Notices
submitted manuscripts, and grant
applications submitted to NIH in 2004,
he falsely claimed that transgenic mice
had been generated with the monofunctional lentiviral vectors with c–
Myc, Ras or Akt under the control of the
CD4 promoter, when they had not, and
that transgenic mice had been generated
with the bi-functional lentiviral vectors
with CD4–c–Myc, Ras or Akt– and U6–
shRNAs targeting luciferase, Bcl–2, or
Bim proteins, when they had not. The
effect of these misrepresentations was
the reported false conclusion that a
cytokine-stimulated proto-oncogene
network regulated CD4+ T-cell survival
and responses to foreign and self
antigens.
8. While at MIT, Dr. Luk Van Parijs
admitted that in presentations and
submitted manuscripts in 2004, he
falsely claimed that mice injected with
plasmids carrying shRNAs for Bcl–2,
Akt1 and Akt2, complexed to
polyethylene imine (PEI) showed a
significant reduction in c–myc-induced
tumor growth, when the experiments
had not been done.
9. While at MIT, Dr. Luk Van Parijs
admitted that in presentations in 2004,
he falsely claimed that shRNAs
designed using algorithms developed in
2004 were more effective to silence
target genes than the shRNAs designed
with algorithms in 2002.
10. While at MIT, Dr. Luk Van Parijs
admitted that in multiple presentations,
submitted manuscripts, a grant
application submitted to NIH, and in the
text of Current Opinions in Molec.
Therapeutics, 6:136, 2004, he falsely
claimed that an in vivo RNAi screen
was developed to identify genes in
cytokine and apoptosis pathways that
accelerated or suppressed Myc-induced
tumorigenesis in lethally irradiated
mice, by using bi-functional lentiviral
vectors that expressed c-Myc under
control of the CMV enhancer-b-actin
promoter (CAG) and U6-driven shRNAs
designed to silence 168 selected genes,
when the experiments had not been
done.
11. While at MIT, Dr. Luk Van Parijs
admitted that in a submitted manuscript
in 2004 and a grant application
submitted to NIH in 2003, he falsely
claimed that with the use of retroviral
vectors with Bim and activated Ras, Akt
or Myc, he showed that the IL–2stimulated activation of proto-oncogene
pathways functioned to promote the
survival of T cells following antigen
encounter by regulating Bim and Bcl–2
pathways, when the experiments that
were performed were inconclusive.
Dr. Van Parijs has entered into a
Voluntary Exclusion Agreement in
which he has voluntarily agreed, for a
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period of five (5) years, beginning on
December 22, 2008:
(1) to exclude himself from any
contracting or subcontracting with any
agency of the United States Government
and from eligibility or involvement in
nonprocurement programs of the United
States Government referred to as
‘‘covered transactions’’ pursuant to
HHS’ Implementation (2 CFR Part 376 et
seq.) of OMB Guidelines to Agencies on
Government wide Debarment and
Suspension (2 CFR, Part 180); and
(2) To exclude himself from serving in
any advisory capacity to PHS, including
but not limited to service on any PHS
advisory committee, board, and/or peer
review committee, or as a consultant.
FOR FURTHER INFORMATION CONTACT:
Director, Division of Investigative
Oversight, Office of Research Integrity,
1101 Wootton Parkway, Suite 750,
Rockville, MD 20852, (240) 453–8800.
The times shown above are for the full
Committee meeting. Subcommittee breakout
sessions can be scheduled for late in the
afternoon of the first day and second day and
in the morning prior to the full Committee
meeting on the second day. Agendas for these
breakout sessions will be posted on the
NCVHS website (URL below) when available.
For Further Information Contact:
Substantive program information as well as
summaries of meetings and a roster of
committee members may be obtained from
Marjorie S. Greenberg, Executive Secretary,
NCVHS, National Center for Health Statistics,
Centers for Disease Control and Prevention,
3311 Toledo Road, Room 2402, Hyattsville,
Maryland 20782, telephone (301) 458–4245.
Information also is available on the NCVHS
home page of the HHS Web site: https://
www.ncvhs.hhs.gov/, where further
information including an agenda will be
posted when available.
Should you require reasonable
accommodation, please contact the CDC
Office of Equal Employment Opportunity on
(301) 458–4EEO (4336) as soon as possible.
Dated: January 14, 2009.
Chris B. Pascal,
Director, Office of Research Integrity.
[FR Doc. E9–1453 Filed 1–22–09; 8:45 am]
Dated: January 12, 2009.
James Scanlon,
Deputy Assistant Secretary for Science and
Data Policy, Office of the Assistant Secretary
for Planning and Evaluation.
[FR Doc. E9–1445 Filed 1–22–09; 8:45 am]
BILLING CODE 4150–31–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Committee on Vital and Health
Statistics: Meeting
Pursuant to the Federal Advisory
Committee Act, the Department of
Health and Human Services (HHS)
announces the following advisory
committee meeting.
Name: National Committee on Vital and
Health Statistics (NCVHS), Full Committee
Meeting.
Time and Date:
February 25, 2009, 9 a.m.–3 p.m. February
26, 2009, 10 a.m.–4 p.m.
Place: Hubert Humphrey Building, 200
Independence Avenue, SW., Room 505A,
Washington, DC 20201.
Status: Open.
Purpose: At this meeting the Committee
will hear presentations and hold discussions
on several health data policy topics. On the
morning of the first day the Committee will
hear updates from the Department, the HHS
Data Council, the Center for Medicare and
Medicaid Services, as well as update on the
transition to the new administration. There
will also be an ONC update on the NHIN
Conference. In the afternoon there will be a
speaker on de-identification of health data
from the Center for Democracy and
Technology.
On the morning of the second day there
will be a briefing on international
terminology and an update on Health
Statistics for the 21st Century. There will also
be an update from NCHS Board of Scientific
Counselors and an overview of emerging and
innovative sources of health data.
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10273]
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.
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23JAN1
mstockstill on PROD1PC66 with NOTICES
Federal Register / Vol. 74, No. 14 / Friday, January 23, 2009 / Notices
1. Type of Information Collection
Request: New collection; Title of
Information Collection: Evaluation of
the Medicare Care Management
Performance Demonstration (MCMP)
and the Electronic Health Records
Demonstration (EHRD); Use: The MCMP
demonstration was authorized under
Section 649 of the Medicare
Prescription Drug, Improvement, and
Modernization Act of 2003. This is a
three year pay for performance
demonstration with physicians to
promote the adoption and use of health
information technology (HIT) to
improve the quality of care for eligible
chronically ill Medicare beneficiaries.
MCMP targets small to medium sized
primary care practices with up to 10
physicians. Practices must provide care
to at least 50 Medicare beneficiaries.
Physicians will receive payments for
meeting or exceeding performance
standards for quality of care. They will
also receive an additional incentive
payment for electronic submission of
performance measures via their
electronic health record (EHR) system.
These payments are in addition to their
normal payments for providing service
to Medicare beneficiaries. The Office
System Survey (OSS) will be used to
assess progress of physician practices in
implementation and use of EHRs and
related HIT functionalities.
The EHR demonstration is authorized
under section 402 of the Medicare
Waiver Authority. The goal of this six
year pay for performance demonstration
is to foster the implementation and
adoption of EHRs and HIT in order to
improve the quality of care provided by
physician practices. The EHRD expands
upon the MCMP Demonstration and
will test whether performance-based
financial incentives (1) increase
physician practices’ adoption and use of
electronic health records (EHRs), and (2)
improve the quality of care that
practices deliver to chronically ill
patients. The EHRD targets small to
medium sized primary care practices
with up to 20 physicians. Practices must
provide care to at least 50 Medicare
beneficiaries. Approximately 2,400
practices will be enrolled in the
demonstration across 12 sites. Practices
will be randomly assigned to a
treatment and control group. The OSS
will be used to assess progress of
physician practices in implementation
and use of EHRs and related HIT
functionalities, and to determine
incentive payments for treatment
practices. In-person and telephone
discussions with community partners
and physician practices will be used to
learn about practices’ experiences and
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strategies in adopting and using EHRs,
as well as the factors that help or hinder
their efforts. Form Number: CMS–10273
(OMB# 0938—New); Frequency:
Annually, Biennially and Once;
Affected Public: Business or other forprofit; Number of Respondents: 3434;
Total Annual Responses: 3434; Total
Annual Hours: 2586.
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/Paperwork
ReductionActof1995, 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.
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 March 24, 2009:
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 l, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: January 14, 2009.
Michelle Shortt,
Director, Regulations Development Group,
Office of Strategic Operations and Regulatory
Affairs.
[FR Doc. E9–1435 Filed 1–22–09; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[CMS–2899–FN]
Medicare and Medicaid Programs;
Approval of the Accreditation
Commission for Health Care,
Incorporated for Continued Deeming
Authority for Home Health Agencies
AGENCY: Centers for Medicare &
Medicaid Services (CMS), HHS.
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ACTION:
4203
Final notice.
SUMMARY: This notice announces our
decision to approve the Accreditation
Commission for Health Care,
Incorporated (ACHC) for continued
recognition as a national accreditation
program for home health agencies
(HHAs) seeking to participate in the
Medicare or Medicaid programs.
DATES: Effective Date: This final notice
is effective February 24, 2009 through
February 24, 2015.
FOR FURTHER INFORMATION CONTACT:
Lillian Williams, (410) 786–8636.
Patricia Chmielewski, (410) 786–6899.
SUPPLEMENTARY INFORMATION:
I. Background
Under the Medicare program, eligible
beneficiaries may receive selected
covered services from a home health
agency (HHA) provided certain
requirements are met. Sections 1861(m)
and (o), 1891, and 1895 of the Social
Security Act (the Act) authorize the
Secretary to establish distinct criteria for
facilities seeking designation as an
HHA. Under this authority, the
minimum requirements that an HHA
must meet to participate in Medicare are
set forth in regulations at 42 CFR part
484 and 42 CFR part 409, which
determine the basis and scope of HHAcovered services, and the conditions for
Medicare payment for home health care.
Regulations concerning provider
agreements are at 42 CFR part 489 and
those pertaining to activities relating to
the survey and certification of facilities
are at 42 CFR part 488.
Generally, to enter into an agreement,
an HHA must first be certified by a State
survey agency as complying with
conditions or requirements set forth in
part 484 of our regulations. Then, the
HHA is subject to regular surveys by a
State survey agency to determine
whether it continues to meet those
requirements. There is an alternative,
however, to surveys by State agencies.
Section 1865(a)(1) of the Act (as
redesignated under section 125 of the
Medicare Improvements for Patients and
Providers Act of 2008 (MIPPA) (Pub. L.
110–275) provides that, if a provider
entity demonstrates through
accreditation by an approved national
accreditation organization that all
applicable Medicare conditions are met
or exceeded, we may ‘‘deem’’ those
provider entities as having met
Medicare requirements. (We note that
section 125 of MIPPA redesignated
subsections (b) through (e) of subsection
1865 of the Act as (a) through (d)
respectively.) Accreditation by an
accreditation organization is voluntary
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Agencies
[Federal Register Volume 74, Number 14 (Friday, January 23, 2009)]
[Notices]
[Pages 4202-4203]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E9-1435]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10273]
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.
[[Page 4203]]
1. Type of Information Collection Request: New collection; Title of
Information Collection: Evaluation of the Medicare Care Management
Performance Demonstration (MCMP) and the Electronic Health Records
Demonstration (EHRD); Use: The MCMP demonstration was authorized under
Section 649 of the Medicare Prescription Drug, Improvement, and
Modernization Act of 2003. This is a three year pay for performance
demonstration with physicians to promote the adoption and use of health
information technology (HIT) to improve the quality of care for
eligible chronically ill Medicare beneficiaries. MCMP targets small to
medium sized primary care practices with up to 10 physicians. Practices
must provide care to at least 50 Medicare beneficiaries. Physicians
will receive payments for meeting or exceeding performance standards
for quality of care. They will also receive an additional incentive
payment for electronic submission of performance measures via their
electronic health record (EHR) system. These payments are in addition
to their normal payments for providing service to Medicare
beneficiaries. The Office System Survey (OSS) will be used to assess
progress of physician practices in implementation and use of EHRs and
related HIT functionalities.
The EHR demonstration is authorized under section 402 of the
Medicare Waiver Authority. The goal of this six year pay for
performance demonstration is to foster the implementation and adoption
of EHRs and HIT in order to improve the quality of care provided by
physician practices. The EHRD expands upon the MCMP Demonstration and
will test whether performance-based financial incentives (1) increase
physician practices' adoption and use of electronic health records
(EHRs), and (2) improve the quality of care that practices deliver to
chronically ill patients. The EHRD targets small to medium sized
primary care practices with up to 20 physicians. Practices must provide
care to at least 50 Medicare beneficiaries. Approximately 2,400
practices will be enrolled in the demonstration across 12 sites.
Practices will be randomly assigned to a treatment and control group.
The OSS will be used to assess progress of physician practices in
implementation and use of EHRs and related HIT functionalities, and to
determine incentive payments for treatment practices. In-person and
telephone discussions with community partners and physician practices
will be used to learn about practices' experiences and strategies in
adopting and using EHRs, as well as the factors that help or hinder
their efforts. Form Number: CMS-10273 (OMB 0938--New);
Frequency: Annually, Biennially and Once; Affected Public: Business or
other for-profit; Number of Respondents: 3434; Total Annual Responses:
3434; Total Annual Hours: 2586.
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 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.
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 March 24, 2009:
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 --, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
Dated: January 14, 2009.
Michelle Shortt,
Director, Regulations Development Group, Office of Strategic Operations
and Regulatory Affairs.
[FR Doc. E9-1435 Filed 1-22-09; 8:45 am]
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