Office of the National Coordinator for Health Information Technology; American Health Information Community Population Health and Clinical Care Connections Workgroup Meeting, 43937 [E8-17314]
Download as PDF
Federal Register / Vol. 73, No. 146 / Tuesday, July 29, 2008 / Notices
The meeting will be available via Web
cast. For additional information, go to:
https://www.hhs.gov/healthit/ahic/
quality/quality_instruct.html.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. E8–17298 Filed 7–28–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology;
American Health Information
Community Confidentiality, Privacy, &
Security Workgroup Meeting
ACTION:
Announcement of meeting.
SUMMARY: This notice announces the
22nd meeting of the American Health
Information Community Confidentiality,
Privacy, & Security Workgroup in
accordance with the Federal Advisory
Committee Act (Pub. L. No. 92–463, 5
U.S.C., App.).
August 21, 2008, from 1 p.m. to
5 p.m. [Eastern Time].
DATES:
Mary C. Switzer Building
(330 C Street, SW., Washington, DC
20201), Conference Room 1114. Please
use the C Street entrance closest to 3rd
Street and bring photo ID for entry to a
Federal building.
ADDRESSES:
FOR FURTHER INFORMATION CONACT:
https://www.hhs.gov/healthit/ahic/
confidentiality/.
The
Workgroup Members will continue
discussing and evaluating the
confidentiality, privacy, and security
protections and requirements for
participants in electronic health
information exchange environments.
The meeting will be available via Web
cast. For additional information, go to:
https://www.hhs.gov/healthit/ahic/
cps_instruct.html.
jlentini on PROD1PC65 with NOTICES
SUPPLEMENTARY INFORMATION:
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. E8–17313 Filed 7–28–08; 8:45 am]
16:12 Jul 28, 2008
Office of the National Coordinator for
Health Information Technology;
American Health Information
Community Population Health and
Clinical Care Connections Workgroup
Meeting
ACTION:
Announcement of meeting.
SUMMARY: This notice announces the
29th meeting of the American Health
Information Community Population
Health and Clinical Care Connections
Workgroup in accordance with the
Federal Advisory Committee Act (Pub.
L. 92–463, 5 U.S.C., App.).
DATES: August 20, 2008, from 2 p.m. to
5 p.m. [Eastern Time].
ADDRESSES: Mary C. Switzer Building
(330 C Street, SW., Washington, DC
20201), Conference Room 1114. Please
use the C Street entrance closest to 3rd
Street and 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. The meeting will be
available via Web cast. For additional
information, go to: https://www.hhs.gov/
healthit/ahic/population/
pop_instruct.html.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. E8–17314 Filed 7–28–08; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2008–N–0389]
Food and Drug Administration
Amendments Act of 2007; Prohibition
Against Food to Which Drugs or
Biological Products Have Been Added;
Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; request for comments.
SUMMARY: The Food and Drug
Administration (FDA) is requesting
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HUMAN SERVICES
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43937
comments relevant to the
implementation of section 912 of the
Food and Drug Administration
Amendments Act of 2007 (FDAAA).
Section 912 of FDAAA establishes
section 301(ll) in the Federal Food,
Drug, and Cosmetic Act (the act), which
prohibits the interstate shipment of
certain foods to which an approved drug
or a licensed biological product has
been added. Section 301(ll) also
prohibits the interstate shipment of
foods containing an added drug or a
biological product that has been the
subject of substantial clinical
investigations, the existence of which
has been made public. FDA requests
that interested persons submit data,
information, and comments that will
help provide a context for the agency’s
decisions on implementation of this
provision. To encourage responsive
comments, FDA is including a series of
questions for interested persons to
consider in preparing comments.
DATES: Submit written or electronic
comments by October 27, 2008.
ADDRESSES: Submit written comments,
data, and other information to the
Division of Dockets Management (HFA–
305), Food and Drug Administration,
5630 Fishers Lane, rm. 1061, Rockville,
MD 20852. Submit electronic comments
to www.regulations.gov.
FOR FURTHER INFORMATION CONTACT:
Catherine L. Copp, Center for Food
Safety and Applied Nutrition (HFS–4),
Food and Drug Administration, 301–
436–1589, e-mail: catherine.copp@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
On September 27, 2007, the Food and
Drug Administration Amendments Act
of 2007 (Public Law 110–85) (FDAAA)
was enacted. Section 912 of FDAAA
establishes section 301(ll) in the Federal
Food, Drug, and Cosmetic Act (the act),
21 U.S.C. 331(ll), which adds the
following prohibited act to section
301.21 U.S.C. 331:
The introduction or delivery for
introduction into interstate commerce of
any food to which has been added a
drug approved under section 505, a
biological product licensed under
section 351 of the Public Health Service
Act, or a drug or a biological product for
which substantial clinical investigations
have been instituted and for which the
existence of such investigations has
been made public, unless-(1) such drug or such biological product
was marketed infood before any approval of
the drug under section 505, beforelicensure
of the biological product under such section
351, andbefore any substantial clinical
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Agencies
[Federal Register Volume 73, Number 146 (Tuesday, July 29, 2008)]
[Notices]
[Page 43937]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-17314]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the National Coordinator for Health Information
Technology; American Health Information Community Population Health and
Clinical Care Connections Workgroup Meeting
ACTION: Announcement of meeting.
-----------------------------------------------------------------------
SUMMARY: This notice announces the 29th meeting of the American Health
Information Community Population Health and Clinical Care Connections
Workgroup in accordance with the Federal Advisory Committee Act (Pub.
L. 92-463, 5 U.S.C., App.).
DATES: August 20, 2008, from 2 p.m. to 5 p.m. [Eastern Time].
ADDRESSES: Mary C. Switzer Building (330 C Street, SW., Washington, DC
20201), Conference Room 1114. Please use the C Street entrance closest
to 3rd Street and 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. The meeting will be available via Web
cast. For additional information, go to: https://www.hhs.gov/healthit/
ahic/population/pop_instruct.html.
Judith Sparrow,
Director, American Health Information Community, Office of Programs and
Coordination, Office of the National Coordinator for Health Information
Technology.
[FR Doc. E8-17314 Filed 7-28-08; 8:45 am]
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