Proposed Data Collections Submitted for Public Comment and Recommendations, 33302-33303 [2011-14145]
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33302
Federal Register / Vol. 76, No. 110 / Wednesday, June 8, 2011 / Notices
No. 0920–0591 exp. 2/28/2011)—
Reinstatement without change—
National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID),
Centers for Disease Control and
Prevention (CDC), officially established
as a substructure on July 9, 2010.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–11–0591]
Agency Forms Undergoing Paperwork
Reduction Act Review
Background and Brief Description
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) 395–5806. Written
comments should be received within 30
days of this notice.
The Centers for Disease Control and
Prevention is requesting a three year
extension to continue data collection
under the Select Agent Distribution
Activity. The form used for this activity
is currently approved under OMB
Control No. 0920–0591. The purpose of
this data collection is to provide a
systematic and consistent mechanism to
review requests that come to CDC for
Select Agents. The term select agents is
used to described a limited group of
viruses, bacteria, rickettsia, and toxins
that have the potential for use as agents
of bioterrorism, inflicting significant
morbidity and mortality on susceptible
populations.
In light of current terrorism concerns
and the significant NIH grant monies
Proposed Project
Select Agent Distribution Activity:
Request for Select Agent (OMB Control
directed toward Select Agent research,
CDC receives hundreds of requests for
Select Agents from researchers. The
approximately 900 applicants are
required to complete an application
form in which they identify themselves
and their institution, provide a
Curriculum Vitae or biographical
sketch, a summary of their research
proposal, and sign indemnification and
material transfer agreement statements.
In this request, CDC is requesting
approval for approximately 450 hours;
no change from the currently approved
burden. The only correction to this data
collection request is updating the name
of the National Center on the
application form. A user fee will be
collected to recover costs for materials,
handling and shipping (except for
public health laboratories). The cost to
the respondent will vary based on
which agent is requested.
Estimate of Annualized Burden Hours
Respondent
Number of respondents
Number of responses per
respondent
Average burden per response (in
hours)
Researcher ..................................................................................................................................
900
1
30/60
Dated: May 31, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–14143 Filed 6–7–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-11–11HD]
sroberts on DSK5SPTVN1PROD with NOTICES
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 or send
comments to Daniel Holcomb, CDC
VerDate Mar<15>2010
21:51 Jun 07, 2011
Jkt 223001
Acting Reports Clearance Officer, 1600
Clifton Road, MS D–74, 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
Study of Comprehensive Cancer
Control and Tobacco Control Program
Partnerships — New — Division of
Cancer Prevention and Control, National
Center for Chronic Disease Prevention
and Health Promotion, Centers for
Disease Control and Prevention (CDC).
PO 00000
Frm 00112
Fmt 4703
Sfmt 4703
Background and Brief Description
Tobacco use remains the leading
preventable cause of death in the United
States, causing over 443,000 deaths each
year and resulting in an annual cost of
more than $96 billion in direct medical
expenses. According to the latest Report
of the Surgeon General (2010), ‘‘How
Tobacco Causes Disease,’’ damage from
tobacco smoke is immediate. Inhaling
the over 7,000 chemicals and
compounds in tobacco smoke causes
immediate and long-term damage and
leads to disease, including cancer, and
death. The only proven strategy for
reducing the risk of tobacco-related
morbidity and mortality is to never
smoke, or to quit if tobacco use has been
initiated.
In 1999, CDC’s Office on Smoking and
Health (OSH) established the National
Tobacco Control Program (NTCP) to
encourage coordinated, national efforts
to reduce tobacco-related morbidity and
mortality. The NTCP provides funding
and technical support to Tobacco
Control Programs (TCPs) in all 50 states,
the District of Columbia, seven tribal
support centers, eight U.S. territories or
jurisdictions, and six national networks.
NTCP awardees implement evidence-
E:\FR\FM\08JNN1.SGM
08JNN1
33303
Federal Register / Vol. 76, No. 110 / Wednesday, June 8, 2011 / Notices
based tobacco control policies and
interventions including telephone
quitlines to increase tobacco use
cessation.
Tobacco control is also a top priority
for federally-funded cancer control
programs. Currently, 65 organizations
are funded through CDC’s National
Comprehensive Cancer Control Program
(NCCCP): all 50 states, the District of
Columbia, seven tribes/tribal
organizations, and seven U.S.
territories/Pacific Island Jurisdictions.
NCCCP grantees are charged with
establishing NCCCP coalitions,
assessing the burden of cancer, and
developing and implementing
comprehensive cancer control (CCC)
plans. The CCC plans address
interventions across the cancer
continuum from primary prevention to
treatment and survivorship. The NCCCP
is managed by CDC’s Division of Cancer
Prevention and Control (DCPC).
CDC recognizes the need for increased
collaboration between CCCs and TCPs.
Toward this end, CDC plans to conduct
a study of current partnership efforts
involving NCCCP awardees and NTCP
awardees. Information will be collected
to improve understanding of the ways in
which CCCs and TCPs may collaborate
to address cancer and tobacco control,
and how these programs utilize their
respective networks to cross-promote
activities. The Partnership Study will be
conducted in seven states that: (1) Are
funded through both the NCCCP and the
NTCP and (2) have an established
relationship between the two programs.
Respondents for the Study of
Comprehensive Cancer Control and
Tobacco Control Program Partnerships
will be state health department leaders,
CCC and TCP staff (e.g., program
directors, evaluation specialists, media
specialists, quitline coordinators), and
other stakeholders, such as coalition
members. Information will be collected
through in-person interviews involving
approximately 15 respondents in each
state. Respondents will be asked about
key aspects of their program’s structure
and activities, including efforts to
coordinate across the CCC–TCP
structure and facilitators and/or barriers
influencing CCC–TCP collaborations.
The questions in each interview will be
customized depending on the
respondent’s role. Each interview will
last approximately 45 minutes to one
hour.
CDC plans to request OMB approval
for one year. The information to be
collected in the Partnership Study will
be used to develop examples of
successful strategies used by selected
CCCs and TCPs to cross-collaborate and
cross-promote programs/services, and to
identify new areas of potential
collaboration that may be shared with
CDC, other federal agencies, and other
CCC and TCP states for replication.
The Partnership Study will
complement and extend the usefulness
of results to be obtained in a companion
study titled ‘‘Comparing the
Effectiveness of Traditional EvidenceBased Tobacco Cessation Interventions
to Newer and Innovative Interventions
Used by Comprehensive Cancer Control
Programs.’’ Additional information
about the companion project will be
published in a separate Federal Register
Notice. Both studies will be funded
through the American Recovery and
Reinvestment Act of 2009 (ARRA).
There are no costs to respondents other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
State Health Department Leadership
Interview Guide for Health Department Leadership.
Site Visit Preparation .......................
49 .....................................................
Site Visit Preparation .......................
49 .....................................................
...........................................................
CCC Programs ..................................
Interview Guide for CCCs .................
Tobacco Control Programs ...............
Interview Guide for TCPs .................
Total ...........................................
Dated: June 1, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease
Control and Prevention.
[FR Doc. 2011–14145 Filed 6–7–11; 8:45 am]
BILLING CODE;P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
sroberts on DSK5SPTVN1PROD with NOTICES
[60Day-11–11GU]
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
VerDate Mar<15>2010
21:51 Jun 07, 2011
Jkt 223001
Frm 00113
Fmt 4703
Total burden
(in hours)
7
1
45/60
5
7
1
7
1
........................
1
1
1
1
........................
45/60
49
45/60
49
113
5
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 Daniel Holcomb, 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
PO 00000
Average burden per response
(in hours)
No. of responses per
respondent
Total number
of respondents
Type of respondent
Sfmt 4703
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
Survey of Rapid Influenza Diagnostic
Test (RIDT) Practices in Clinical
Laboratories—New—the Office of
Surveillance, Epidemiology, and
Laboratory Services (OSELS), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
The Survey of Rapid Influenza
Diagnostic Testing Practices in Clinical
Laboratories is a national systematic
study investigating rapid influenza
diagnostic testing practices in clinical
E:\FR\FM\08JNN1.SGM
08JNN1
5
Agencies
[Federal Register Volume 76, Number 110 (Wednesday, June 8, 2011)]
[Notices]
[Pages 33302-33303]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-14145]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-11-11HD]
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 or
send comments to Daniel Holcomb, CDC Acting Reports Clearance Officer,
1600 Clifton Road, MS D-74, 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
Study of Comprehensive Cancer Control and Tobacco Control Program
Partnerships -- New -- Division of Cancer Prevention and Control,
National Center for Chronic Disease Prevention and Health Promotion,
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
Tobacco use remains the leading preventable cause of death in the
United States, causing over 443,000 deaths each year and resulting in
an annual cost of more than $96 billion in direct medical expenses.
According to the latest Report of the Surgeon General (2010), ``How
Tobacco Causes Disease,'' damage from tobacco smoke is immediate.
Inhaling the over 7,000 chemicals and compounds in tobacco smoke causes
immediate and long-term damage and leads to disease, including cancer,
and death. The only proven strategy for reducing the risk of tobacco-
related morbidity and mortality is to never smoke, or to quit if
tobacco use has been initiated.
In 1999, CDC's Office on Smoking and Health (OSH) established the
National Tobacco Control Program (NTCP) to encourage coordinated,
national efforts to reduce tobacco-related morbidity and mortality. The
NTCP provides funding and technical support to Tobacco Control Programs
(TCPs) in all 50 states, the District of Columbia, seven tribal support
centers, eight U.S. territories or jurisdictions, and six national
networks. NTCP awardees implement evidence-
[[Page 33303]]
based tobacco control policies and interventions including telephone
quitlines to increase tobacco use cessation.
Tobacco control is also a top priority for federally-funded cancer
control programs. Currently, 65 organizations are funded through CDC's
National Comprehensive Cancer Control Program (NCCCP): all 50 states,
the District of Columbia, seven tribes/tribal organizations, and seven
U.S. territories/Pacific Island Jurisdictions. NCCCP grantees are
charged with establishing NCCCP coalitions, assessing the burden of
cancer, and developing and implementing comprehensive cancer control
(CCC) plans. The CCC plans address interventions across the cancer
continuum from primary prevention to treatment and survivorship. The
NCCCP is managed by CDC's Division of Cancer Prevention and Control
(DCPC).
CDC recognizes the need for increased collaboration between CCCs
and TCPs. Toward this end, CDC plans to conduct a study of current
partnership efforts involving NCCCP awardees and NTCP awardees.
Information will be collected to improve understanding of the ways in
which CCCs and TCPs may collaborate to address cancer and tobacco
control, and how these programs utilize their respective networks to
cross-promote activities. The Partnership Study will be conducted in
seven states that: (1) Are funded through both the NCCCP and the NTCP
and (2) have an established relationship between the two programs.
Respondents for the Study of Comprehensive Cancer Control and
Tobacco Control Program Partnerships will be state health department
leaders, CCC and TCP staff (e.g., program directors, evaluation
specialists, media specialists, quitline coordinators), and other
stakeholders, such as coalition members. Information will be collected
through in-person interviews involving approximately 15 respondents in
each state. Respondents will be asked about key aspects of their
program's structure and activities, including efforts to coordinate
across the CCC-TCP structure and facilitators and/or barriers
influencing CCC-TCP collaborations. The questions in each interview
will be customized depending on the respondent's role. Each interview
will last approximately 45 minutes to one hour.
CDC plans to request OMB approval for one year. The information to
be collected in the Partnership Study will be used to develop examples
of successful strategies used by selected CCCs and TCPs to cross-
collaborate and cross-promote programs/services, and to identify new
areas of potential collaboration that may be shared with CDC, other
federal agencies, and other CCC and TCP states for replication.
The Partnership Study will complement and extend the usefulness of
results to be obtained in a companion study titled ``Comparing the
Effectiveness of Traditional Evidence-Based Tobacco Cessation
Interventions to Newer and Innovative Interventions Used by
Comprehensive Cancer Control Programs.'' Additional information about
the companion project will be published in a separate Federal Register
Notice. Both studies will be funded through the American Recovery and
Reinvestment Act of 2009 (ARRA). There are no costs to respondents
other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
No. of Average burden
Type of respondent Form name Total number responses per per response Total burden
of respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
State Health Department Interview Guide 7 1 45/60 5
Leadership. for Health
Department
Leadership.
CCC Programs.................. Site Visit 7 1 45/60 5
Preparation.
Interview Guide for CCCs...... 49.............. 1 1 49
Tobacco Control Programs...... Site Visit 7 1 45/60 5
Preparation.
Interview Guide for TCPs...... 49.............. 1 1 49
Total..................... ................ .............. .............. 113
----------------------------------------------------------------------------------------------------------------
Dated: June 1, 2011.
Daniel Holcomb,
Reports Clearance Officer, Centers for Disease Control and Prevention.
[FR Doc. 2011-14145 Filed 6-7-11; 8:45 am]
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