Disease, Disability, and Injury Prevention and Control Special Emphasis Panel (SEP): Occupational Health and Safety Research, Program Announcement 04038 and Small Grants in Occupational Safety and Health, Program Announcement 04021, 75465 [E5-7550]
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Federal Register / Vol. 70, No. 243 / Tuesday, December 20, 2005 / Notices
product label even absent those
requirements.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
William Blumenthal,
General Counsel.
[FR Doc. E5–7531 Filed 12–19–05; 8:45 am]
Food and Drug Administration
BILLING CODE 6750–01–P
Notice of Approval of Supplemental
New Animal Drug Application;
Tilmicosin
AGENCY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
ACTION:
Centers for Disease Control and
Prevention
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Occupational
Health and Safety Research, Program
Announcement 04038 and Small
Grants in Occupational Safety and
Health, Program Announcement 04021
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC)
announces the following meeting:
Name: Disease, Disability, and Injury
Prevention and Control Special Emphasis
Panel (SEP): Occupational Health and Safety
Research, Program Announcement 04038 and
Small Grants in Occupational Safety and
Health, Program Announcement 04021.
Time and Date: 1 p.m.–3 p.m., January 13,
2006 (Closed).
Place: National Institute for Occupational
Safety and Health, CDC, 1600 Clifton Road,
NE., Mailstop E–74, Atlanta, GA 30333
Telephone Number (404) 498–2582.
Status: The meeting will be closed to the
public in accordance with provisions set
forth in section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director,
Management Analysis and Services Office,
CDC, pursuant to Public Law 92–463.
Matters To Be Considered: The meeting
will include the review, discussion, and
evaluation of applications received in
response to: Occupational Health and Safety
Research, Program Announcement 04038 and
Small Grants in Occupational Safety and
Health, Program Announcement 04021.
Contact Person For More Information:
Charles Rafferty, Ph.D., Scientific Review
Administrator, National Institute for
Occupational Safety and Health, CDC, 1600
Clifton Road, NE., Mailstop E–74, Atlanta,
GA 30333, Telephone Number (404) 498–
2582. The Director, Management Analysis
and Services Office, has been delegated the
authority to sign Federal Register notices
pertaining to announcements of meetings and
other committee management activities, for
both CDC and the Agency for Toxic
Substances and Disease Registry.
Dated: December 13, 2005.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E5–7550 Filed 12–19–05; 8:45 am]
BILLING CODE 4163–18–P
VerDate Aug<31>2005
19:23 Dec 19, 2005
Jkt 208001
Food and Drug Administration,
HHS.
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is providing
notice that it has approved a
supplemental new animal drug
application (NADA) filed by Elanco
Animal Health. The approved NADA
provides for the veterinary prescription
use of an injectable solution of
tilmicosin phosphate for respiratory
disease in cattle and sheep. This
supplemental NADA adds user safety
information to product labeling.
FOR FURTHER INFORMATION CONTACT: Joan
C. Gotthardt, Center for Veterinary
Medicine (HFV–130), Food and Drug
Administration, 7500 Standish Pl.,
Rockville, MD 20855, 301–827–7571, email: joan.gotthardt@fda.gov.
SUPPLEMENTARY INFORMATION: Elanco
Animal Health, A Division of Eli Lilly
& Co., Lilly Corporate Center,
Indianapolis, IN 46285, filed a
supplement to NADA 140–929 for
MICOTIL 300 (tilmicosin phosphate), an
injectable solution available by
veterinary prescription for use in the
treatment and control of respiratory
disease in cattle and in the treatment of
respiratory disease in sheep. This
supplemental NADA adds user safety
information to product labeling related
to the mechanism of toxicity and
medical intervention. In accordance
with section 512(i) of the Federal Food,
Drug, and Cosmetic Act (the act) (21
U.S.C. 360b(i)) and part 514 (21 CFR
part 514) in §§ 514.105(a) and
514.106(a), the Center for Veterinary
Medicine is providing notice that this
supplemental NADA is approved as of
December 2, 2005. The basis of approval
is discussed in the freedom of
information summary.
In accordance with the freedom of
information provisions of 21 CFR part
20 and § 514.11(e)(2)(ii), a summary of
safety and effectiveness data and
information submitted to support
approval of this application may be seen
in the Division of Dockets Management
(HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852, between 9
a.m. and 4 p.m., Monday through
Friday.
PO 00000
Frm 00021
Fmt 4703
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75465
FDA has determined under 21 CFR
25.33(a)(1) that this action is of a type
that does not individually or
cumulatively have a significant effect on
the human environment. Therefore,
neither an environmental assessment
nor an environmental impact statement
is required.
Dated: December 8, 2005.
Bernadette Dunham,
Deputy Director, Office of New Animal Drug
Evaluation, Center for Veterinary Medicine.
[FR Doc. 05–24269 Filed 12–19–05; 8:45 am]
BILLING CODE 4160–01–S
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2005N–0485]
Regulatory Process for Pediatric
Mechanical Circulatory Support
Devices (Ventricular Assist Devices)
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of public meeting.
SUMMARY: The Food and Drug
Administration (FDA) is announcing the
following public meeting: Regulatory
Process for Pediatric Mechanical
Circulatory Support Devices
(Ventricular Assist Devices). The topics
of discussion are the agency’s activities
regarding the regulation and approval of
circulatory support devices used for
temporary support in pediatric patients.
Date and Time: The public meeting
will be held on January 20, 2006, from
9 a.m. to 12 p.m. The agency is
requiring registration by December 30,
2005.
Location: The public meeting will be
held at the Center for Devices and
Radiological Health, rm. 20B, 9200
Corporate Blvd., Rockville, MD 20850.
Contact: Eric Chen, Center for Devices
and Radiological Health (HFZ–450),
Food and Drug Administration, 9200
Corporate Blvd., 301–443–8262, ext.
146, e-mail: eac@cdrh.fda.gov, or
Michael Berman (HFZ–170), 12725
Twinbrook Pkwy., 301–827–4744, email: mrb@cdrh.fda.gov. If you need
special accommodations due to a
disability, please contact Eric Chen, at
least 7 days in advance of the meeting.
Registration: There is no fee to attend
the workshop; however, because space
is limited, registration is required.
Please submit registration information
(including name, title, firm name,
address, e-mail address, telephone
number, and fax number) by December
30, 2005 (see Contact). Background
information for the workshop will be
E:\FR\FM\20DEN1.SGM
20DEN1
Agencies
[Federal Register Volume 70, Number 243 (Tuesday, December 20, 2005)]
[Notices]
[Page 75465]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E5-7550]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Disease, Disability, and Injury Prevention and Control Special
Emphasis Panel (SEP): Occupational Health and Safety Research, Program
Announcement 04038 and Small Grants in Occupational Safety and Health,
Program Announcement 04021
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), the Centers for Disease Control and
Prevention (CDC) announces the following meeting:
Name: Disease, Disability, and Injury Prevention and Control
Special Emphasis Panel (SEP): Occupational Health and Safety
Research, Program Announcement 04038 and Small Grants in
Occupational Safety and Health, Program Announcement 04021.
Time and Date: 1 p.m.-3 p.m., January 13, 2006 (Closed).
Place: National Institute for Occupational Safety and Health,
CDC, 1600 Clifton Road, NE., Mailstop E-74, Atlanta, GA 30333
Telephone Number (404) 498-2582.
Status: The meeting will be closed to the public in accordance
with provisions set forth in section 552b(c)(4) and (6), Title 5
U.S.C., and the Determination of the Director, Management Analysis
and Services Office, CDC, pursuant to Public Law 92-463.
Matters To Be Considered: The meeting will include the review,
discussion, and evaluation of applications received in response to:
Occupational Health and Safety Research, Program Announcement 04038
and Small Grants in Occupational Safety and Health, Program
Announcement 04021.
Contact Person For More Information: Charles Rafferty, Ph.D.,
Scientific Review Administrator, National Institute for Occupational
Safety and Health, CDC, 1600 Clifton Road, NE., Mailstop E-74,
Atlanta, GA 30333, Telephone Number (404) 498-2582. The Director,
Management Analysis and Services Office, has been delegated the
authority to sign Federal Register notices pertaining to
announcements of meetings and other committee management activities,
for both CDC and the Agency for Toxic Substances and Disease
Registry.
Dated: December 13, 2005.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. E5-7550 Filed 12-19-05; 8:45 am]
BILLING CODE 4163-18-P