Proposed Data Collections Submitted for Public Comment and Recommendations, 41205-41206 [2010-17267]
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Federal Register / Vol. 75, No. 135 / Thursday, July 15, 2010 / Notices
FOR FURTHER INFORMATION CONTACT:
Sandra M. Peay, Contact Representative
or Renee Chapman, Contact
Representative.
Federal Trade Commission, Premerger
Notification Office, Bureau Of
Competition, Room H–303 Washington,
DC 20580, (202) 326–3100.
By direction of the Commission.
Donald S. Clark,
Secretary.
[FR Doc. 2010–17051 Filed 7–14–10; 8:45 am]
BILLING CODE 6750–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
CDC is requesting continued OMB
approval to collect this information
through the use of two separate forms.
These forms are: (1) Application for
Permit to Import or Transport Etiologic
Agents, Hosts, or Vectors of Human
Disease; and (2) Application for Permit
to Import or Transport Live Bats.
The Application for Permit to Import
or Transport Etiologic Agents, Hosts, or
Vectors of Human Disease will be used
by laboratory facilities, such as those
operated by government agencies,
universities, research institutions, and
zoologic exhibitions, and also by
importers of nonhuman primate trophy
materials, such as hunters or
taxidermists, to request permits for the
importation of etiologic agents, hosts, or
vectors of human disease. The
Application for Permit to Import or
Transport Etiologic Agents, Hosts, or
Vectors of Human Disease requests
applicant and sender contact
information; description of material for
importation; facility isolation and
containment information; and personnel
qualifications.
The Application for Permit to Import
or Transport Live Bats will be used by
laboratory facilities such as those
operated by government agencies,
universities, research institutions, and
zoologic exhibitions entities to request
importation and subsequent distribution
after importation of live bats. The
Application for Permit to Import or
Transport Live Bats requests applicant
and sender contact information; a
description and intended use of bats to
be imported; facility isolation and
containment information; and personnel
qualifications.
There is no cost to respondents except
their time.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Centers for Disease Control and
Prevention
[60Day–FY10–0199]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
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, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Maryam I. Daneshvar,
CDC Reports Clearance Officer, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an e-mail to
omb@cdc.gov.
41205
Importation of Transportation of
Etiologic Agents (42 CFR 71.54)—(OMB
Control No. 0920–0199 exp. 1/31/
2011)—Extension—Office of Public
Health Preparedness and Response
(OPHPR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Foreign Quarantine Regulations
(42 CFR part 71) set forth provisions to
prevent the introduction, transmission,
and spread of communicable disease
from foreign countries into the United
States. Subpart F—Importations—
contains provisions for importation of
etiologic agents, hosts, and vectors (42
CFR part 71.54), requiring persons that
import these materials to obtain a
permit issued by the CDC. This request
is for the information collection
requirements contained in 42 CFR 71.54
for issuance of permits by CDC to
importers of etiologic agents, hosts, or
vectors of human disease.
ESTIMATED ANNUALIZED BURDEN HOURS
No. of
respondents
Respondents
No. of
responses per
respondent
2,000
10
1
1
Total ..........................................................................................................
srobinson on DSKHWCL6B1PROD with NOTICES
Applicants ........................................................................................................
Applicants ........................................................................................................
........................
........................
VerDate Mar<15>2010
17:49 Jul 14, 2010
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Average
burden per
response
(in hours)
Total burden
(in hours)
20/60
20/60
667
3
........................
669
41206
Federal Register / Vol. 75, No. 135 / Thursday, July 15, 2010 / Notices
Date: July 8, 2010.
Carol Walker,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
Management and Budget, Washington,
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
[FR Doc. 2010–17267 Filed 7–14–10; 8:45 am]
Proposed Project
BILLING CODE 4163–18–P
A three-year approval is being sought
with the current data collection
instrument. The data collection
instrument has been valuable in
assessing performance and capacity and
identifying areas for improvement.
From 1998–2002, the National Public
Health Performance Standards Program
convened workgroups with the National
Association of County and City Health
Officials (NACCHO), The Association of
State and Territorial Health Officials
(ASTHO), the National Association of
Local Boards of Health (NALBOH), the
American Public Health Association
(APHA), and the Public Health
Foundation (PHF) to develop
performance standards for public health
systems based on the essential services
of public health. In 2005, CDC
reconvened workgroups with these
same organizations to revise the data
collection instruments, in order to
ensure the standards remain current and
improve user friendliness. There is no
cost to the respondent, other than their
time. The estimated annualized burden
hours are 5600.
National Public Health Performance
Standards Program Local Public Health
System Assessment (OMB 0920–0555
exp. 8/31/10)—Extension—Office of
State, Tribal, Local and Territorial
Support, Centers for Disease Control
and Prevention (CDC).
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–10–0555]
Background and Brief Description
Agency Forms Undergoing Paperwork
Reduction Act Review
The Office of State, Tribal, Local and
Territorial Support is proposing to
extend the formal, voluntary data
collection that assesses the capacity of
local public health systems to deliver
the essential services of public health.
Local health departments will respond
to the survey on behalf of the collective
body of representatives from the local
public health system. Electronic data
submission will be used when local
public health agencies complete the
public health assessment.
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
e-mail to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
ESTIMATE OF ANNUALIZED BURDEN HOURS
Type of respondents
Form name
No. of
respondents
No. of
responses per
respondent
Average
burden per
response
(in hours)
Local Public Health System ............................
Local Public Health System Performance Assessment Instrument.
350
1
16
Dated: July 9, 2010.
Thelma Sims,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
Management and Budget, Washington,
DC or by fax to (202) 395–5806. Written
comments should be received within 30
days of this notice.
[FR Doc. 2010–17273 Filed 7–14–10; 8:45 am]
Proposed Project
BILLING CODE 4163–18–P
Monitoring and Reporting System for
Chronic Disease Prevention and Control
Programs—New—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Background and Brief Description
[30-Day–10–10DT]
srobinson on DSKHWCL6B1PROD with NOTICES
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
VerDate Mar<15>2010
16:53 Jul 14, 2010
Jkt 220001
Although chronic diseases are among
the most common and costly health
problems, they are also among the most
preventable. The Centers for Disease
Control and Prevention (CDC) works
with states, territories, tribal
organizations, and the District of
Columbia (collectively referred to as
‘‘state-based’’ programs) to develop,
implement, manage, and evaluate
chronic disease prevention and control
programs. Support and guidance for
these programs have been provided
through cooperative agreement funding
and technical assistance, administered
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
by CDC’s National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP). Partnerships
and collaboration with other Federal
agencies, nongovernmental
organizations, local communities,
public and private sector organizations,
and major voluntary associations have
been critical to the success of these
efforts.
CDC seeks OMB approval for three
years to collect progress and activity
information from health departments
funded for four program areas: Tobacco
control, diabetes prevention and
control, Healthy Communities, and
state-based behavioral risk factor
surveillance. Information will be
collected electronically through a new,
electronic Management Information
System (MIS). Information will be
collected on each program area’s
objectives, planning activities,
resources, partnerships, policy and
environmental strategies for preventing
or controlling chronic diseases, and
progress toward meeting goals. The new
MIS harmonizes the progress reporting
framework for all program areas and
E:\FR\FM\15JYN1.SGM
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]]>Agencies
[Federal Register Volume 75, Number 135 (Thursday, July 15, 2010)]
[Notices]
[Pages 41205-41206]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-17267]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-FY10-0199]
Proposed Data Collections Submitted for Public Comment and
Recommendations
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, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960
and send comments to Maryam I. Daneshvar, CDC Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
to omb@cdc.gov.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; and (d) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology. Written comments should be received
within 60 days of this notice.
Proposed Project
Importation of Transportation of Etiologic Agents (42 CFR 71.54)--
(OMB Control No. 0920-0199 exp. 1/31/2011)--Extension--Office of Public
Health Preparedness and Response (OPHPR), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Foreign Quarantine Regulations (42 CFR part 71) set forth
provisions to prevent the introduction, transmission, and spread of
communicable disease from foreign countries into the United States.
Subpart F--Importations--contains provisions for importation of
etiologic agents, hosts, and vectors (42 CFR part 71.54), requiring
persons that import these materials to obtain a permit issued by the
CDC. This request is for the information collection requirements
contained in 42 CFR 71.54 for issuance of permits by CDC to importers
of etiologic agents, hosts, or vectors of human disease.
CDC is requesting continued OMB approval to collect this
information through the use of two separate forms. These forms are: (1)
Application for Permit to Import or Transport Etiologic Agents, Hosts,
or Vectors of Human Disease; and (2) Application for Permit to Import
or Transport Live Bats.
The Application for Permit to Import or Transport Etiologic Agents,
Hosts, or Vectors of Human Disease will be used by laboratory
facilities, such as those operated by government agencies,
universities, research institutions, and zoologic exhibitions, and also
by importers of nonhuman primate trophy materials, such as hunters or
taxidermists, to request permits for the importation of etiologic
agents, hosts, or vectors of human disease. The Application for Permit
to Import or Transport Etiologic Agents, Hosts, or Vectors of Human
Disease requests applicant and sender contact information; description
of material for importation; facility isolation and containment
information; and personnel qualifications.
The Application for Permit to Import or Transport Live Bats will be
used by laboratory facilities such as those operated by government
agencies, universities, research institutions, and zoologic exhibitions
entities to request importation and subsequent distribution after
importation of live bats. The Application for Permit to Import or
Transport Live Bats requests applicant and sender contact information;
a description and intended use of bats to be imported; facility
isolation and containment information; and personnel qualifications.
There is no cost to respondents except their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
No. of Average burden
Respondents No. of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
Applicants.................................... 2,000 1 20/60 667
Applicants.................................... 10 1 20/60 3
-----------------------------------------------------------------
Total..................................... .............. .............. ............... 669
----------------------------------------------------------------------------------------------------------------
[[Page 41206]]
Date: July 8, 2010.
Carol Walker,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2010-17267 Filed 7-14-10; 8:45 am]
BILLING CODE 4163-18-P
