Anti-Infective Drugs Advisory Committee Meeting; Amendment of Notice, 51833 [06-7310]
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Federal Register / Vol. 71, No. 169 / Thursday, August 31, 2006 / Notices
electronically each every fiscal year at
https://www.grants.gov.
Joan E. Ohl,
Commissioner, Administration on Children,
Youth and Families.
[FR Doc. 06–7364 Filed 8–30–06; 8:45 am]
BILLING CODE 4184–01–P
Dated: August 25, 2006.
Randall W. Lutter,
Associate Commissioner for Policy and
Planning.
[FR Doc. 06–7310 Filed 8–30–06; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
Anti-Infective Drugs Advisory
Committee Meeting; Amendment of
Notice
AGENCY:
BILLING CODE 4160–01–S
Food and Drug Administration,
HHS.
ACTION:
Notice.
erjones on PROD1PC72 with NOTICES
15:29 Aug 30, 2006
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
The Food and Drug
Administration (FDA) is announcing an
amendment to the notice of a meeting of
the Anti-Infective Drugs Advisory
Committee. This meeting was
announced in the Federal Register of
July 25, 2006 (71 FR 42096). The
amendment is being made to reflect a
change in the Date and Time and
Agenda portions of the document. The
meeting scheduled for September 11,
2006, has been cancelled. There are no
other changes.
FOR FURTHER INFORMATION CONTACT:
Sohail Mosaddegh, 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:
sohail.mosaddegh@fda.hhs.gov, or FDA
Advisory Committee Information Line,
1–800–741–8138 (301–443–0572 in the
Washington DC area), code 3014512530.
Please call the Information Line for upto-date information on this meeting.
SUPPLEMENTARY INFORMATION: In the
Federal Register of July 25, 2006 (71 FR
42096), FDA announced that a meeting
of the Anti-Infective Drugs would be
held on September 11 and 12, 2006. On
page 42096, in the second column, the
Date and Time portion of the meeting is
amended to read as follows:
Date and Time: The meeting will held
on September 12, 2006, from 8 a.m. to
5 p.m.
On page 42096, third column, the
Agenda portion of the meeting is
amended to read as follows:
Agenda: On September 12, 2006, the
committee will discuss supplemental
SUMMARY:
VerDate Aug<31>2005
new drug application (sNDA) 21–158/S–
006, FACTIVE (gemifloxacin mesylate)
Tablets, submitted by Oscient
Pharmaceuticals Corp., for the proposed
treatment of acute baterial sinusitis.
This notice is issued under the
Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14,
relating to advisory committees.
Jkt 208001
Proposed Data Collection; Comment
Request; California Health Interview
Survey 2007
SUMMARY: In compliance with the
requirement of Section 3506(c)(2)(A) of
the Paperwork Reduction Act of 1995
for opportunity for public comment on
proposed data collection projects,
National Cancer Institute (NCI), the
National Institute of Health (NIH) will
publish periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
The first California Health Interview
Survey (CHIS) Cancer Control Module
(CCM) took place in 2001 (2000 CHIS
CCM, OMB No. 0925–0478, Federal
Register, May 8, 2000, Vol. 65, No. 89,
p. 26620). The second survey took place
in 2003 (2003 CHIS CCM, OMB No.
0925–0518, Federal Register, October 3,
2002, Volume 67, No. 192, pp. 62067–
62068) and the third in 2005 (2005 CHIS
CCM, OMB No. 0925–0000, Federal
Register, Vol. 69, No. 150, Aug. 5, 2004,
pp. 47450–47451, and Federal Register,
Vol. 70, No. 1, Jan. 3, 2005, pp. 93–94).
Proposed Collection
Title: California Health Interview
Survey (CHIS) 2007 Cancer Control
Module (CCM). Type of Information
Collection Request: New. Need and Use
of Information Collection: The NCI has
sponsored three Cancer Control
Modules in the California Health
Interview Survey (CHIS), and will be
sponsoring a fourth to be administered
in 2007.
The CHIS is a telephone survey
designed to provide population-based,
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
51833
standardized health-related data to
assess California’s progress in meeting
Healthy People 2010 objectives for the
nation and the state. The CHIS sample
is designed to provide statistically
reliable estimates statewide, for
California counties, and for California’s
ethnically and racially diverse
population. Initiated by the UCLA
Center for Health Policy Research, the
California Department of Health
Services, and the California Public
Health Institute, the survey is funded by
a number of public and private sources.
It was first administered in 2001 to
55,428 adults and subsequently in 2003
and 2005 to 42,043 and 43,020 adults
respectively. These adults are a
representative sample of California’s
non-institutionalized population living
in households.
CHIS 2007, the fourth bi-annual
survey, is planned for administration to
55,000 adult Californians. The cancer
control module, which is similar to that
administered in CHIS 2001, CHIS 2003,
and CHIS 2005, will allow NCI to
examine trends in breast cancer
screening and diagnosis, as well as to
study other cancer-related topics such
as diet, physical activity, and obesity.
Because California is the most
populous and the most racially and
ethnically diverse state in the nation,
the CHIS 2007 sample will yield
adequate numbers of respondents in key
ethnic and racial groups, including
African Americans, Latinos, Asians, and
American Indian/Alaska Natives. The
Latino group will include large numbers
of respondents in the Mexican, Central
American, South American, and other
Latino subgroups; the Asian group will
include large numbers of respondents in
the Chinese, Filipino, Japanese,
Vietnamese, and Korean subgroups. NCI
will compare the CHIS and National
Health Interview Survey (NHIS) data in
order to conduct comparative analyses
and better estimate cancer risk factors
and screening among racial/ethnic
minority populations. The CHIS sample
size also permits NCI to create estimates
for ethnic subdomains of the
population, for which NHIS has
insufficient numbers for analysis.
Frequency of Response: One-time.
Affected public: Individuals or
households. Types of Respondents: U.S.
adults (persons 18 years of age and
older).
The annual reporting burden is as
follows.
E:\FR\FM\31AUN1.SGM
31AUN1
Agencies
[Federal Register Volume 71, Number 169 (Thursday, August 31, 2006)]
[Notices]
[Page 51833]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 06-7310]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
Anti-Infective Drugs Advisory Committee Meeting; Amendment of
Notice
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is announcing an
amendment to the notice of a meeting of the Anti-Infective Drugs
Advisory Committee. This meeting was announced in the Federal Register
of July 25, 2006 (71 FR 42096). The amendment is being made to reflect
a change in the Date and Time and Agenda portions of the document. The
meeting scheduled for September 11, 2006, has been cancelled. There are
no other changes.
FOR FURTHER INFORMATION CONTACT: Sohail Mosaddegh, 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:
sohail.mosaddegh@fda.hhs.gov, or FDA Advisory Committee Information
Line, 1-800-741-8138 (301-443-0572 in the Washington DC area), code
3014512530. Please call the Information Line for up-to-date information
on this meeting.
SUPPLEMENTARY INFORMATION: In the Federal Register of July 25, 2006 (71
FR 42096), FDA announced that a meeting of the Anti-Infective Drugs
would be held on September 11 and 12, 2006. On page 42096, in the
second column, the Date and Time portion of the meeting is amended to
read as follows:
Date and Time: The meeting will held on September 12, 2006, from 8
a.m. to 5 p.m.
On page 42096, third column, the Agenda portion of the meeting is
amended to read as follows:
Agenda: On September 12, 2006, the committee will discuss
supplemental new drug application (sNDA) 21-158/S-006, FACTIVE
(gemifloxacin mesylate) Tablets, submitted by Oscient Pharmaceuticals
Corp., for the proposed treatment of acute baterial sinusitis.
This notice is issued under the Federal Advisory Committee Act (5
U.S.C. app. 2) and 21 CFR part 14, relating to advisory committees.
Dated: August 25, 2006.
Randall W. Lutter,
Associate Commissioner for Policy and Planning.
[FR Doc. 06-7310 Filed 8-30-06; 8:45 am]
BILLING CODE 4160-01-S