Advisory Committee for Injury Prevention and Control: Notice of Charter Renewal, 66334-66335 [E6-19151]
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66334
Federal Register / Vol. 71, No. 219 / Tuesday, November 14, 2006 / Notices
Dated: November 6, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–19146 Filed 11–13–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–07–0604]
Agency Forms Undergoing Paperwork
Reduction Act Review
The Centers for Disease Control and
Prevention (CDC) publishes a list of
information collection requests under
review by the Office of Management and
Budget (OMB) in compliance with the
Paperwork Reduction Act (44 U.S.C.
Chapter 35). To request a copy of these
requests, call the CDC Reports Clearance
Officer at (404) 639–5960 or send an email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
DC or by fax to (202) 395–6974. Written
comments should be received within 30
days of this notice.
Proposed Project
School Associated Violent Death
Surveillance System—Extension—
National Center for Injury Prevention
and Control (NCIPC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Division of Violence Prevention
(DVP), National Center for Injury
Prevention and Control (NCIPC)
proposes to maintain a system for the
surveillance of school-associated
homicides and suicides. The system
will rely on existing public records and
interviews with law enforcement
officials and school officials. The
purpose of the system is to (1) estimate
the rate of school-associated violent
death in the United States and (2)
identify common features of schoolassociated violent deaths. The system
will contribute to the understanding of
fatal violence associated with schools,
guide further research in the area, and
help direct ongoing and future
prevention programs.
Violence is the leading cause of death
among young people, and increasingly
recognized as an important public
health and social issue. In 1998, over
3,500 school aged children (5 to 18
years old) in the United States died
violent deaths due to suicide, homicide,
and unintentional firearm injuries. The
vast majority of these fatal injuries were
not school associated. However,
whenever a homicide or suicide occurs
in or around school, it becomes a matter
of particularly intense public interest
and concern. NCIPC conducted the first
scientific study of school-associated
violent deaths during the 1992–99
academic years to establish the true
extent of this highly visible problem.
Despite the important role of schools as
a setting for violence research and
prevention interventions, relatively
little scientific or systematic work has
been done to describe the nature and
level of fatal violence associated with
schools. Until NCIPC conducted the first
nationwide investigation of violent
deaths associated with schools, public
health and education officials had to
rely on limited local studies and
estimated numbers to describe the
extent of school-associated violent
death.
The system will draw cases from the
entire United States in attempting to
capture all cases of school-associated
violent deaths that have occurred.
Investigators will review public records
and published press reports concerning
each school-associated violent death.
For each identified case, investigators
will also interview an investigating law
enforcement official (defined as a police
officer, police chief, or district attorney),
and a school official (defined as a school
principal, school superintendent, school
counselor, school teacher, or school
support staff) who are knowledgeable
about the case in question. Researchers
will request information on both the
victim and alleged offender(s)—
including demographic data, their
academic and criminal records, and
their relationship to one another. They
will also collect data on the time and
location of the death; the circumstances,
motive, and method of the fatal injury;
and the security and violence
prevention activities in the school and
community where the death occurred,
before and after the fatal injury event.
There are no costs to the respondents
other than their time. The total
estimated annualized burden hours are
70.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Respondents
School Officials ............................................................................................................................
Police Officials .............................................................................................................................
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
BILLING CODE 4163–18–P
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Dated: November 7, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–19147 Filed 11–13–06; 8:45 am]
Advisory Committee for Injury
Prevention and Control: Notice of
Charter Renewal
Centers for Disease Control and
Prevention
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the
Advisory Committee for Injury
Prevention and Control, Centers for
Disease Control and Prevention,
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Number of
responses per
respondent
Average burden/response
(in hours)
1
1
1
1
35
35
Department of Health and Human
Services, has been renewed for a 2-year
period through October 28, 2008.
For information, contact Amy Harris,
Executive Secretary, Advisory
Committee for Injury Prevention and
Control, Centers for Disease Control and
Prevention, Department of Health and
Human Services, 1600 Clifton Road,
NE., Mailstop K61, Atlanta, Georgia
30333, telephone 770/488–1484 or fax
770/488–4222.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
E:\FR\FM\14NON1.SGM
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66335
Federal Register / Vol. 71, No. 219 / Tuesday, November 14, 2006 / Notices
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: November 6, 2006.
Alvin Hall,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E6–19151 Filed 11–13–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 2006N–0329]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Medicated Feed
Mill License Application
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Fax written comments on the
collection of information by December
14, 2006
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–6974.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of the Chief
Information Officer (HFA–250), Food
and Drug Administration, 5600 Fishers
Lane, Rockville, MD 20857, 301–827–
1472.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Medicated Feed Mill Licensing
Application—21 CFR Part 515 (OMB
Control No. 0910–0337)—Extension
The Animal Drug Availability Act
(ADAA) of October 9, 1996, amended
section 512 of the Federal Food, Drug,
and Cosmetic Act (21 U.S.C. 360b) to
replace the system for the approval of
specific medicated feed with a general
licensing system for feed mills. Before
passage of the ADAA, medicated feed
manufacturers were required to obtain
approval of Medicated Feed
Applications (MFAs) in order to
manufacture certain types of medicated
feeds. An individual approved MFA
was required for each and every
applicable medicated feed. The ADAA
streamlined the paperwork process for
gaining approval to manufacture
medicated feeds by replacing the MFA
system with a facility license for each
medicated feed manufacturing facility.
Implementing regulations are at part 515
(21 CFR part 515).
In the Federal Register of August 25,
2006 (71 FR 50433), FDA solicited
comments on the information collection
provisions of this proposed collection.
In response to that request, FDA
received no comments.
Description of Respondents:
Medicated feed manufacturers.
FDA estimates the burden for this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN1
21 CFR Section
No. of Respondents
515.10(b)
515.11(b)
515.23
515.30(c)
Total
1There
Annual Frequency per
Response
7
100
25
0.15
Total Annual Responses
1
1
1
1
Hours per
Response
7
100
25
0.15
Total Hours
0.25
0.25
0.25
24
1.75
25
6.25
3.6
36.6
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 2.—ESTIMATED ANNUAL RECORDKEEPING BURDEN1
No. of Recordkeepers
Annual Frequency
per Recordkeeping
Total Annual Records
1,070
21 CFR Section
1
1,070
510.305
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1There
Hours per Recordkeeper
Total Hours
0.03
32.10
are no capital costs or operating and maintenance costs associated with this collection of information.
The estimated annual reporting
burden on industry is 36.6 hours as
shown in table 1 of this document.
Industry estimates it takes about 1/4
hour to submit the application. We
estimate 132 original and supplemental
applications, and voluntary revocations
for a total of 33 hours (132 submissions
x 1/4 hour). An additional 3.6 hours is
added for the rare notice of opportunity
for a hearing to not approve or revoke
an application. Finally, we estimate 36
hours for maintaining and retrieving
labels as required by 21 CFR 510.305.
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We estimated .03 hours for each of
approximately 1,070 licensees. Thus,
the total burden for recordkeeping
requirements is 32.10 hours (1,070 x
0.03).
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Dated: November 7, 2006.
Jeffrey Shuren,
Assistant Commissioner for Policy.
[FR Doc. E6–19152 Filed 11–13–06; 8:45 am]
[Docket No. 2006D–0441]
BILLING CODE 4160–01–S
PO 00000
Food and Drug Administration
Draft Guidance for Industry: Protocols
for the Conduct of Method Transfer
Studies for Type C Medicated Feed
Assay Methods; Availability
AGENCY:
Food and Drug Administration,
HHS.
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[Federal Register Volume 71, Number 219 (Tuesday, November 14, 2006)]
[Notices]
[Pages 66334-66335]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-19151]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Advisory Committee for Injury Prevention and Control: Notice of
Charter Renewal
This gives notice under the Federal Advisory Committee Act (Pub. L.
92-463) of October 6, 1972, that the Advisory Committee for Injury
Prevention and Control, Centers for Disease Control and Prevention,
Department of Health and Human Services, has been renewed for a 2-year
period through October 28, 2008.
For information, contact Amy Harris, Executive Secretary, Advisory
Committee for Injury Prevention and Control, Centers for Disease
Control and Prevention, Department of Health and Human Services, 1600
Clifton Road, NE., Mailstop K61, Atlanta, Georgia 30333, telephone 770/
488-1484 or fax 770/488-4222.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register notices pertaining to
announcements of
[[Page 66335]]
meetings and other committee management activities, for both the
Centers for Disease Control and Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: November 6, 2006.
Alvin Hall,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. E6-19151 Filed 11-13-06; 8:45 am]
BILLING CODE 4163-18-P
