Anesthetic and Life Support Drugs Advisory Committee; Notice of Meeting, 5723-5724 [E7-1991]
Download as PDF
Federal Register / Vol. 72, No. 25 / Wednesday, February 7, 2007 / Notices
20201), Conference Room 4090 (please
bring photo ID for entry to a Federal
building).
FOR FURTHER INFORMATION CONTACT:
https://www.hhs.gov/healthit/ahic/
confidentiality/.
The
Workgroup members will discuss
supplemental Identity Proofing
Recommendations and Workgroup
priorities for the rest of the year. The
Workgroup plans to publish questions
for public comment in the Federal
Register before this meeting.
This meeting will be available via
Web cast at https://www.hhs.gov/
healthit/ahic/cps_instruct.html.
SUPPLEMENTARY INFORMATION:
BILLING CODE 4150–24–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology,
American Health Information
Community Electronic Health Records
Workgroup Meeting
ACTION:
Dated: January 30, 2007.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. 07–514 Filed 2–6–07; 8:45 am]
BILLING CODE 4150–24–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the National Coordinator for
Health Information Technology;
American Health Information
Community Personalized Healthcare
Workgroup Meeting
ACTION:
Dated: January 29, 2007.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. 07–515 Filed 2–6–07; 8:45 am]
Announcement of meeting.
SUMMARY: This notice announces the
2nd meeting of the American Health
Information Community Personalized
Healthcare Workgroup in accordance
with the Federal Advisory Committee
Act (Pub. L. No. 92–463, 5 U.S.C., App.).
February 21, 2007, from 1 p.m.
to 3 p.m.
DATES:
Mary C. Switzer Building
(330 C Street, SW., Washington, DC
20201), Conference Room 4090 (please
bring photo ID for entry to a Federal
building).
ADDRESSES:
Announcement of meeting.
SUMMARY: This notice announces the
13th meeting of the American Health
Information Community Electronic
Health Records Workgroup in
accordance with the Federal Advisory
Committee Act (Pub. L. No. 92–463, 5
U.S.C., App.).
DATES: February 22, 2007, from 1 p.m.
to 4 p.m./Eastern.
ADDRESSES: Mary C. Switzer Building
(330 C Street, SW., Washington, DC
20201), Conference Room 4090 (please
bring photo ID for entry to a Federal
building).
FOR FURTHER INFORMATION CONTACT:
https://www.hhs.gov/healthit/ahic/
healthrecords/.
SUPPLEMENTARY INFORMATION: The
workgroup will continue its discussion
of the barriers and drivers of EHR
adoption. For additional information, go
to https://www.hhs.gov/healthit/ahic/
healthrecords/ehr_instruct.html.
Dated: January 29, 2007.
Judith Sparrow,
Director, American Health Information
Community, Office of Programs and
Coordination, Office of the National
Coordinator for Health Information
Technology.
[FR Doc. 07–516 Filed 2–6–07; 8:45 am]
BILLING CODE 4150–24–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
FOR FURTHER INFORMATION CONTACT:
Food and Drug Administration
https://www.hhs.gov/healthit/ahic/
healthcare/.
The
Workgroup will discuss standards for
personalized healthcare and upcoming
visioning exercise. For additional
information, go to https://www.hhs.gov/
healthit/ahic/healthcare/
phc_instruct.html.
sroberts on PROD1PC70 with NOTICES
SUPPLEMENTARY INFORMATION:
VerDate Aug<31>2005
21:36 Feb 06, 2007
Jkt 211001
Anesthetic and Life Support Drugs
Advisory Committee; Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
5723
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Anesthetic and
Life Support Drugs Advisory
Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on March 29, 2007, from 8 a.m. to
5 p.m.
Location: Doubletree Hotel &
Executive Meeting Center, 1750
Rockville Pike, Rockville, MD. The hotel
telephone number is 301–468–1100.
Contact Person: Cathy A. Groupe,
Center for Drug Evaluation and Research
(HFD–21), Food and Drug
Administration, 5600 Fishers Lane (for
express delivery, 5630 Fishers Lane, rm.
1093), Rockville, MD 20857, 301–827–
7001, FAX: 301–827–6776, e-mail:
Cathy.Groupe@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), code
3014512529. Please call the information
line for up-to-date information on this
meeting.
Agenda: The committee will do the
following: (1) Receive presentations
regarding neurodegenerative findings in
juvenile animals exposed to anesthetic
drugs (e.g., ketamine); and (2) discuss
the relevance of these findings to
pediatric patients and provide guidance
for future preclinical and clinical
studies.
FDA intends to make background
material available to the public no later
than 1 business day before the meeting.
If FDA is unable to post background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/ohrms/
dockets/ac/acmenu.htm, click on the
year 2007 and scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before March 15, 2007.
Oral presentations from the public will
be scheduled between approximately 1
p.m. to 2 p.m. Those desiring to make
formal oral presentations should notify
the contact person and submit a brief
statement of the general nature of the
evidence or arguments they wish to
present, the names and addresses of
E:\FR\FM\07FEN1.SGM
07FEN1
5724
Federal Register / Vol. 72, No. 25 / Wednesday, February 7, 2007 / Notices
proposed participants, and an
indication of the approximate time
requested to make their presentation on
or before March 7, 2007. Time allotted
for each presentation may be limited. If
the number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak on or before March 8,
2007.
Persons attending FDA’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
a disability, please contact Cathy
Groupe at least 7 days in advance of the
meeting.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app. 2).
Dated: February 1, 2007.
Randall W. Lutter,
Associate Commissioner for Policy and
Planning.
[FR Doc. E7–1991 Filed 2–6–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Antiviral Drugs Advisory Committee;
Notice of Meeting
AGENCY:
Food and Drug Administration,
HHS.
sroberts on PROD1PC70 with NOTICES
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Antiviral Drugs
Advisory Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on April 24, 2007, from 8 a.m. to
4 p.m.
Location: Food and Drug
Administration, Center for Drug
Evaluation and Research Advisory
Committee Conference Room, rm. 1066,
5630 Fishers Lane, Rockville, MD.
VerDate Aug<31>2005
21:36 Feb 06, 2007
Jkt 211001
Contact Person: Cicely Reese, Center
for Drug Evaluation and Research (HFD–
21), Food and Drug Administration,
5600 Fishers Lane (for express delivery,
5630 Fishers Lane, rm. 1093) Rockville,
MD 20857, 301–827–7001, FAX: 301–
827–6776, e-mail:
cicely.reese@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington, DC area), code
3014512531. Please call the Information
Line for up-to-date information on this
meeting.
Agenda: The committee will discuss
new drug application (NDA) 022–128,
maraviroc 300 milligram tablets, Pfizer,
Inc., proposed for the treatment of
antiretroviral-experienced patients with
chemokine (c-c motif) receptor 5
(CCR5)—tropic human
immunodeficiency virus (HIV).
FDA intends to make background
material available to the public no later
than 1 business day before the meeting.
If FDA is unable to post the background
material on its Web site prior to the
meeting, the background material will
be made publicly available at the
location of the advisory committee
meeting, and the background material
will be posted on FDA’s Web site after
the meeting. Background material is
available at https://www.fda.gov/ohrms/
dockets/ac/acmenu.htm, click on the
year 2007 and scroll down to the
appropriate advisory committee link.
Procedure: Interested persons may
present data, information, or views,
orally or in writing, on issues pending
before the committee. Written
submissions may be made to the contact
person on or before April 3, 2007. Oral
presentations from the public will be
scheduled between approximately 1
p.m. and 2 p.m. Those desiring to make
formal oral presentations should notify
the contact person and submit a brief
statement of the general nature of the
evidence or arguments they wish to
present, the names and addresses of
proposed participants, and an
indication of the approximate time
requested to make their presentation on
or before March 26, 2007. Time allotted
for each presentation may be limited. If
the number of registrants requesting to
speak is greater than can be reasonably
accommodated during the scheduled
open public hearing session, FDA may
conduct a lottery to determine the
speakers for the scheduled open public
hearing session. The contact person will
notify interested persons regarding their
request to speak by March 27, 2007.
Persons attending FDA’s advisory
committee meetings are advised that the
agency is not responsible for providing
access to electrical outlets.
PO 00000
Frm 00050
Fmt 4703
Sfmt 4703
FDA welcomes the attendance of the
public at its advisory committee
meetings and will make every effort to
accommodate persons with physical
disabilities or special needs. If you
require special accommodations due to
adisability, please contact Cicely Reese
at least 7 days in advance of the
meeting.
Notice of this meeting is given under
the Federal Advisory Committee Act (5
U.S.C. app 2).
Dated: February 1, 2007.
Randall W. Lutter,
Associate Commissioner for Policy and
Planning.
[FR Doc. E7–1900 Filed 2–6–07; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Vaccines and Related Biological
Products Advisory Committee; Notice
of Meeting
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
This notice announces a forthcoming
meeting of a public advisory committee
of the Food and Drug Administration
(FDA). The meeting will be open to the
public.
Name of Committee: Vaccines and
Related Biological Products Advisory
Committee.
General Function of the Committee:
To provide advice and
recommendations to the agency on
FDA’s regulatory issues.
Date and Time: The meeting will be
held on February 27, 2007, from 8 a.m.
to 5:30 p.m. and on February 28, 2007,
from 8 a.m. to 4:15 p.m.
Location: Hilton Hotel, Washington
DC North/Gaithersburg, 620 Perry
Pkwy., Gaithersburg, MD 20877.
Contact Person: Christine Walsh or
Denise Royster, Center for Biologics
Evaluation and Research (HFM–71),
Food and Drug Administration, 1401
Rockville Pike, Rockville, MD 20852,
301–827–0314, or FDA Advisory
Committee Information Line, 1–800–
741–8138 (301–443–0572 in the
Washington, DC area), code 301–451–
2391. Please call the Information Line
for up-to-date information on this
meeting.
Agenda: On February 27, 2007, in the
morning session, the committee will
hear presentations and make
recommendations on the safety and
effectiveness of an H5N1 inactivated
E:\FR\FM\07FEN1.SGM
07FEN1
Agencies
[Federal Register Volume 72, Number 25 (Wednesday, February 7, 2007)]
[Notices]
[Pages 5723-5724]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E7-1991]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Anesthetic and Life Support Drugs Advisory Committee; Notice of
Meeting
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
This notice announces a forthcoming meeting of a public advisory
committee of the Food and Drug Administration (FDA). The meeting will
be open to the public.
Name of Committee: Anesthetic and Life Support Drugs Advisory
Committee.
General Function of the Committee: To provide advice and
recommendations to the agency on FDA's regulatory issues.
Date and Time: The meeting will be held on March 29, 2007, from 8
a.m. to 5 p.m.
Location: Doubletree Hotel & Executive Meeting Center, 1750
Rockville Pike, Rockville, MD. The hotel telephone number is 301-468-
1100.
Contact Person: Cathy A. Groupe, Center for Drug Evaluation and
Research (HFD-21), Food and Drug Administration, 5600 Fishers Lane (for
express delivery, 5630 Fishers Lane, rm. 1093), Rockville, MD 20857,
301-827-7001, FAX: 301-827-6776, e-mail: Cathy.Groupe@fda.hhs.gov, or
FDA Advisory Committee Information Line, 1-800-741-8138 (301-443-0572
in the Washington, DC area), code 3014512529. Please call the
information line for up-to-date information on this meeting.
Agenda: The committee will do the following: (1) Receive
presentations regarding neurodegenerative findings in juvenile animals
exposed to anesthetic drugs (e.g., ketamine); and (2) discuss the
relevance of these findings to pediatric patients and provide guidance
for future preclinical and clinical studies.
FDA intends to make background material available to the public no
later than 1 business day before the meeting. If FDA is unable to post
background material on its Web site prior to the meeting, the
background material will be made publicly available at the location of
the advisory committee meeting, and the background material will be
posted on FDA's Web site after the meeting. Background material is
available at https://www.fda.gov/ohrms/dockets/ac/acmenu.htm, click on
the year 2007 and scroll down to the appropriate advisory committee
link.
Procedure: Interested persons may present data, information, or
views, orally or in writing, on issues pending before the committee.
Written submissions may be made to the contact person on or before
March 15, 2007. Oral presentations from the public will be scheduled
between approximately 1 p.m. to 2 p.m. Those desiring to make formal
oral presentations should notify the contact person and submit a brief
statement of the general nature of the evidence or arguments they wish
to present, the names and addresses of
[[Page 5724]]
proposed participants, and an indication of the approximate time
requested to make their presentation on or before March 7, 2007. Time
allotted for each presentation may be limited. If the number of
registrants requesting to speak is greater than can be reasonably
accommodated during the scheduled open public hearing session, FDA may
conduct a lottery to determine the speakers for the scheduled open
public hearing session. The contact person will notify interested
persons regarding their request to speak on or before March 8, 2007.
Persons attending FDA's advisory committee meetings are advised
that the agency is not responsible for providing access to electrical
outlets.
FDA welcomes the attendance of the public at its advisory committee
meetings and will make every effort to accommodate persons with
physical disabilities or special needs. If you require special
accommodations due to a disability, please contact Cathy Groupe at
least 7 days in advance of the meeting.
Notice of this meeting is given under the Federal Advisory
Committee Act (5 U.S.C. app. 2).
Dated: February 1, 2007.
Randall W. Lutter,
Associate Commissioner for Policy and Planning.
[FR Doc. E7-1991 Filed 2-6-07; 8:45 am]
BILLING CODE 4160-01-S