HIT Policy Committee's Meaningful Use Workgroup Meetings; Notice of Meetings and Request for Comments, 2910-2911 [2011-885]
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Federal Register / Vol. 76, No. 11 / Tuesday, January 18, 2011 / Notices
means and instrumentalities for the
commission of deceptive acts and
practices, and accordingly, themselves
committed a deceptive act in violation
of Section 5 of the FTC Act.
The Commission also alleges that by
stating that the NGBA and the NAGC
endorsed Tested Green, respondents
represented expressly or impliedly that
they were independent from these
organizations, when, in fact, they own
and operate NGBA and NAGC.
Therefore, respondents’ statement of
endorsement by NGBA and NAGC was
false and misleading, in violation of
Section 5. Similarly, in light of
respondents’ express and implied
representation that these organizations
were independent, respondents’ failure
to disclose their relationship to NGBA
and NAGC was deceptive, in violation
of Section 5.
Part I of the proposed order prohibits
respondents from misrepresenting: (1)
The fact that, or degree to which, they
have, or a third party has, evaluated a
product, package, service, practice, or
program based on its environmental
benefits or attributes; (2) that
respondents have, or a third party has,
the appropriate expertise to evaluate the
environmental benefits or attributes of a
product, package, service, practice, or
program; (3) the number of certifications
issued by respondents; and (4) that a
product, package, certification, service,
practice, or program is endorsed by an
independent person or organization.
Part II of the proposed order bars
respondents, in connection with the
labeling, advertising, marketing,
promotion, offering for sale, sale, or
distribution of any product, package,
certification, service, practice, or
program, from providing others with the
means and instrumentalities to make,
expressly or impliedly, any false or
misleading statement.
Part III of the proposed order bars
respondents from making any
representation, expressly or by
implication, about any user or endorser
of a product, package, certification,
service, practice, or program, unless
they clearly and prominently disclose a
material connection with such user or
endorser, where one exists.
Parts IV through VIII of the proposed
order are reporting and compliance
provisions. Part IV requires respondents
to retain documents relating to their
compliance with the order. Part V
requires dissemination of the order to
all current and future principals,
officers, directors, managers, employees,
agents, and representatives having
responsibilities relating to the subject
matter of the order. Part VI ensures
notification to the FTC of changes in
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respondent Nonprofit Management’s
corporate status. Part VII mandates that
respondent Claeys notify the FTC of any
changes in his business affiliations or
employment. Part VIII mandates that
respondents submit a report to the
Commission detailing their compliance
with the order. Part IX provides that the
order expires after twenty (20) years,
with certain exceptions.
The purpose of this analysis is to aid
public comment on the proposed order.
It is not intended to constitute an
official interpretation of the proposed
order or to modify its terms in any way.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2011–926 Filed 1–14–11; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the National Vaccine
Advisory Committee
Office of the Assistant
Secretary for Health, Office of the
Secretary, Department of Health and
Human Services.
ACTION: Notice of meeting.
AGENCY:
As stipulated by the Federal
Advisory Committee Act, the
Department of Health and Human
Services (DHHS) is hereby giving notice
that the National Vaccine Advisory
Committee (NVAC) will hold a meeting.
The meeting is open to the public. Preregistration is required for both public
attendance and comment. Individuals
who wish to attend the meeting and/or
participate in the public comment
session should either e-mail
nvpo@hhs.gov or call 202–690–5566 to
register and provide name, organization,
and e-mail address.
DATES: The meeting will be held on
February 16, 2011 from 8:30 a.m. to 5
p.m., EDT, and February 17, 2011 from
8:30 am to 4 p.m., EDT.
ADDRESSES: Department of Health and
Human Services; Hubert H. Humphrey
Building, Room 800, 200 Independence
Avenue, SW., Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT:
National Vaccine Program Office,
Department of Health and Human
Services, Room 715–H, Hubert H.
Humphrey Building, 200 Independence
Avenue, SW., Washington, DC 20201.
Phone: (202) 690–5566; Fax: (202) 260–
1165; e-mail: nvpo@hhs.gov.
SUPPLEMENTARY INFORMATION: Pursuant
to Section 2101 of the Public Health
Service Act (42 U.S.C. 300aa–1), the
SUMMARY:
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Secretary of Health and Human Services
was mandated to establish the National
Vaccine Program to achieve optimal
prevention of human infectious diseases
through immunization and to achieve
optimal prevention against adverse
reactions to vaccines. The National
Vaccine Advisory Committee was
established to provide advice and make
recommendations to the Director of the
National Vaccine Program on matters
related to the program’s responsibilities.
The Assistant Secretary for Health
serves as Director of the National
Vaccine Program.
Topics to be discussed at the meeting
include the National Vaccine Plan,
Influenza 2010–2011 Season, H1N1
Vaccine Safety, and other related issues.
The meeting agenda will be posted on
the Web site: https://www.hhs.gov/nvpo/
nvac at least one week prior to the
meeting. Public attendance at the
meeting is limited to space available.
Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
notify the National Vaccine Program
Office at the address/phone listed above
at least one week prior to the meeting.
Members of the public will have the
opportunity to provide comments at the
meeting. Public comment will be
limited to five minutes per speaker.
Individuals who would like to submit
written statements should e-mail or fax
their comments to the National Vaccine
Program Office at least five business
days prior to the meeting.
Dated: January 7, 2011.
Bruce Gellin,
Deputy Assistant Secretary for Health,
Director, National Vaccine Program Office.
[FR Doc. 2011–868 Filed 1–14–11; 8:45 am]
BILLING CODE 4150–44–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
HIT Policy Committee’s Meaningful
Use Workgroup Meetings; Notice of
Meetings and Request for Comments
Office of the National
Coordinator for Health Information
Technology, HHS.
ACTION: Notice of Meetings and request
for comments.
AGENCY:
This notice announces the
forthcoming subcommittee meetings of a
Federal advisory committee of the
Office of the National Coordinator for
Health Information Technology (ONC).
The meeting will be open to the public.
Name of Subcommittee: HIT Policy
Committee Meaningful Use Workgroup.
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Federal Register / Vol. 76, No. 11 / Tuesday, January 18, 2011 / Notices
General Function of the
Subcommittee: to provide
recommendations to the HIT Policy
Committee on recommendations it
should consider issuing to the National
Coordinator on future stages of
meaningful use.
Date and Time: The Meaningful Use
Workgroup will hold the following
public meetings between January and
March (dates past March have not yet
been determined):
• Tuesday, March 8, 2011, 10 a.m. to
1 p.m./EDT;
• Tuesday, March 22, 2011, 10 a.m. to
1 p.m./EDT;
• Early April, 2011, date and time
TBD.
Location: All workgroup meetings
will be available via webcast; visit
https://healthit.hhs.gov for instructions
on how to listen via telephone or Web.
Please check the ONC Web site for
additional information as it becomes
available.
Contact Person: Judy Sparrow, Office
of the National Coordinator, HHS, 330 C
Street, SW., Washington, DC 20201,
202–205–4528, Fax: 202–690–6079, email: judy.sparrow@hhs.gov. Please call
the contact person for up-to-date
information on these meetings. A notice
in the Federal Register about last
minute modifications that affect a
previously announced advisory
committee meeting cannot always be
published quickly enough to provide
timely notice.
Agenda: At each meeting, the
Meaningful Use Workgroup will engage
in discussions regarding the
recommendations it should make to the
HIT Policy Committee relative to
meaningful use Stage 2.
Procedure: In order to inform its
deliberations, the Meaningful Use
Workgroup is seeking comments
particularly on proposed stage 2
measures from the public on a draft
document of preliminary
recommendations it has developed.
Please refer to ONC’s Web site at
https://healthit.hhs.gov to access this
draft document and for more
information about how to submit
comments.
Persons attending ONC’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
ONC welcomes the attendance of the
public at its advisory committee
meetings. Seating is limited at the
location, and ONC will make every
effort to accommodate persons with
physical disabilities or special needs. If
you require special accommodations
due to a disability, please contact Judy
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Sparrow at least seven (7) days in
advance of the meeting.
ONC is committed to the orderly
conduct of its advisory committee
meetings. Please visit our Web site at
https://healthit.hhs.gov for procedures
on public conduct during advisory
committee meetings.
Notice of this meeting is given under
the Federal Advisory Committee Act
(Pub. L. 92–463, 5 U.S.C., App. 2).
Dated: January 11, 2011.
Judith Sparrow,
Office of Programs and Coordination, Office
of the National Coordinator for Health
Information Technology.
[FR Doc. 2011–885 Filed 1–12–11; 4:15 pm]
BILLING CODE 4150–45–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project: ‘‘Barriers
to Meaningful Use in Medicaid.’’ In
accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by March 21, 2011.
ADDRESSES: Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection
plans, data collection instruments, and
specific details on the estimated burden
can be obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at doris.lefkowitz@AHRQ.hhs.
gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
Proposed Project
Barriers to Meaningful Use in Medicaid
The Health Information Technology
for Economic and Clinical Health
(HITECH) Act, Title XIII of Division A
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and Title IV of Division B of the
American Recovery and Reinvestment
Act of 2009 (ARRA) (Pub. L. 111–5),
provides for financial incentives for
Medicaid providers to adopt and
meaningfully use certified electronic
health record (EHR) technologies. To
ensure that eligible professionals (EPs)
are able to qualify for and access these
incentives, AHRQ proposes a two-year
project with the objective of
understanding the barriers that
Medicaid health providers encounter
along the way to achieving the
meaningful use of EHRs. This proposed
information collection will allow AHRQ
to synthesize knowledge regarding the
barriers that BPs encounter when
attempting to achieve meaningful use
and translate that knowledge to develop
technical assistance and support
implementation and use of EHRs.
Further, health care providers who
serve Medicaid beneficiaries are serving
many of AHRQ’s priority populations:
Inner city; rural; low income; minority;
women; children; elderly; and those
with special health care needs. The
project is designed to solicit actionable
recommendations on what activities can
best help Medicaid providers take
advantage of incentive payments,
achieve meaningful use, and ultimately
use health IT to improve health care for
the Medicaid population. The
information gathered under this project
will also be used to inform the
development of the Stage 2 and 3
Meaningful Use criteria.
In order to gather, analyze, and
synthesize information on the barriers to
the meaningful use criteria experienced
by Medicaid providers this research has
the following goals:
(1) Identify the barriers to eligibility
for the incentive payments; barriers to
adoption, implementation, or upgrading
of ERR systems; and barriers to
achieving meaningful use.
(2) Develop actionable
recommendations to overcoming the
barriers identified in #1 above,
including, but not limited to, technical
assistance that could be made available
to Medicaid providers.
(3) Provide data to inform the
meaningful use objectives being
developed by the Center for Medicare &
Medicaid Services (CMS) for Stages 2
and 3 of the EHR Incentive Program.
This study is being conducted by
AHRQ through its contractor, RTI
International, pursuant to AHRQ’s
statutory authority to conduct and
support research to advance both
training for health care practitioners in
the use of information systems and the
use of computer-based health records.
42 U.S.C. 299b–3(a)(2) and (6).
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Agencies
[Federal Register Volume 76, Number 11 (Tuesday, January 18, 2011)]
[Notices]
[Pages 2910-2911]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-885]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
HIT Policy Committee's Meaningful Use Workgroup Meetings; Notice
of Meetings and Request for Comments
AGENCY: Office of the National Coordinator for Health Information
Technology, HHS.
ACTION: Notice of Meetings and request for comments.
-----------------------------------------------------------------------
This notice announces the forthcoming subcommittee meetings of a
Federal advisory committee of the Office of the National Coordinator
for Health Information Technology (ONC). The meeting will be open to
the public.
Name of Subcommittee: HIT Policy Committee Meaningful Use
Workgroup.
[[Page 2911]]
General Function of the Subcommittee: to provide recommendations to
the HIT Policy Committee on recommendations it should consider issuing
to the National Coordinator on future stages of meaningful use.
Date and Time: The Meaningful Use Workgroup will hold the following
public meetings between January and March (dates past March have not
yet been determined):
Tuesday, March 8, 2011, 10 a.m. to 1 p.m./EDT;
Tuesday, March 22, 2011, 10 a.m. to 1 p.m./EDT;
Early April, 2011, date and time TBD.
Location: All workgroup meetings will be available via webcast;
visit https://healthit.hhs.gov for instructions on how to listen via
telephone or Web. Please check the ONC Web site for additional
information as it becomes available.
Contact Person: Judy Sparrow, Office of the National Coordinator,
HHS, 330 C Street, SW., Washington, DC 20201, 202-205-4528, Fax: 202-
690-6079, e-mail: judy.sparrow@hhs.gov. Please call the contact person
for up-to-date information on these meetings. A notice in the Federal
Register about last minute modifications that affect a previously
announced advisory committee meeting cannot always be published quickly
enough to provide timely notice.
Agenda: At each meeting, the Meaningful Use Workgroup will engage
in discussions regarding the recommendations it should make to the HIT
Policy Committee relative to meaningful use Stage 2.
Procedure: In order to inform its deliberations, the Meaningful Use
Workgroup is seeking comments particularly on proposed stage 2 measures
from the public on a draft document of preliminary recommendations it
has developed. Please refer to ONC's Web site at https://healthit.hhs.gov to access this draft document and for more information
about how to submit comments.
Persons attending ONC's advisory committee meetings are advised
that the agency is not responsible for providing access to electrical
outlets.
ONC welcomes the attendance of the public at its advisory committee
meetings. Seating is limited at the location, and ONC will make every
effort to accommodate persons with physical disabilities or special
needs. If you require special accommodations due to a disability,
please contact Judy Sparrow at least seven (7) days in advance of the
meeting.
ONC is committed to the orderly conduct of its advisory committee
meetings. Please visit our Web site at https://healthit.hhs.gov for
procedures on public conduct during advisory committee meetings.
Notice of this meeting is given under the Federal Advisory
Committee Act (Pub. L. 92-463, 5 U.S.C., App. 2).
Dated: January 11, 2011.
Judith Sparrow,
Office of Programs and Coordination, Office of the National Coordinator
for Health Information Technology.
[FR Doc. 2011-885 Filed 1-12-11; 4:15 pm]
BILLING CODE 4150-45-P