Proposed Data Collections Submitted for Public Comment and Recommendations, 12739-12740 [E8-4651]
Download as PDF
12739
Federal Register / Vol. 73, No. 47 / Monday, March 10, 2008 / Notices
Dated: February 29, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–4650 Filed 3–7–08; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60 Day–08–08AS]
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 Acting 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
Surveys of BioSense Trainings,—
New—National Center for Public Health
Informatics (NCPHI), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
Congress passed the Public Health
Security and Bioterrorism Preparedness
and Response Act of 2002, which
requires specific activities related to
bioterrorism preparedness and response.
This congressional mandate outlines the
need for improving the overall public’s
health through electronic surveillance.
The Department of Health and Human
Services outlined strategies aimed at
achieving this goal via the Public Health
IT Initiative thereby creating the
BioSense program.
BioSense is the national, human
health surveillance system designed to
improve the nation’s capabilities for
disease detection, monitoring, and realtime health situational awareness. This
work is enhanced by providing public
health real-time access to existing data
from healthcare organizations, state
syndromic surveillance systems,
national laboratories, and others for just
in time public health decision-making.
BioSense data are analyzed through
advanced statistical methods, and made
accessible through the BioSense
application. The application provides
data, charts, graphs, and maps through
a secure web-based interface which can
be accessed by CDC and authorized state
and local public health and hospital
users.
In order to meet the congressional
mandate, it is important that BioSense
users understand the role of BioSense in
daily surveillance as well as be able to
use specific BioSense modalities to
investigate or monitor any potential
disease outbreaks and/or bioterrorist
attacks. A series of training tools have
been developed to educate BioSense
users about how best to utilize BioSense
in these circumstances.
The training tools were developed
based upon a 2007 needs assessment
conducted among BioSense users.
Training 1 is an online, self-paced
training module designed for BioSense
users at the beginner level who are not
wholly familiar with BioSense or have
not used the system on a regular basis.
This module presents the background of
BioSense and an overview of its general
functions in a didactic training style.
Training 2 is a virtual training filmed in
Second Life. It is designed for
intermediate to advanced level users
who are aware of and have used the
general BioSense functionalities for
daily surveillance but want additional
skills related to using BioSense during
an emergency scenario. This scenariobased module is presented in an
experiential training style.
Data collection will take place in the
form of an online survey immediately
following each training module and a
link to an online survey emailed 3months post training. This data
collection will assess the goals of these
trainings, which are to help registered
BioSense users (1) establish knowledge
and efficacy necessary to use BioSense
to investigate and/or monitor a potential
event or outbreak; (2) facilitate
communication between BioSense
administrators in public health and
hospital settings; (3) access BioSense
trainings that are engaging and easy to
use; and (4) use BioSense to investigate
and/or monitor a potential event or
outbreak. The post-training and 3-month
follow-up surveys have been pre-tested
with less than 9 participants. Survey
results will be used to identify the
impact and applicability of these
training modules for BioSense users.
There are no costs to survey
respondents other than their time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form
Number of
responses per
respondent
Average burden
per response
(in hours)
Total burden
(in hours)
400
320
1
1
10/60
5/60
67
27
Total ..................................................................................
pwalker on PROD1PC71 with NOTICES
Post-Training Survey ...............................................................
3–Month Follow Up Survey .....................................................
..............................
..............................
..............................
94
VerDate Aug<31>2005
16:39 Mar 07, 2008
Jkt 214001
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
E:\FR\FM\10MRN1.SGM
10MRN1
12740
Federal Register / Vol. 73, No. 47 / Monday, March 10, 2008 / Notices
Dated: February 29, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E8–4651 Filed 3–7–08; 8:45 am]
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Centers for Disease Control and
Prevention
BILLING CODE 4163–18–P
Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): ‘‘Annual
Estimates of Influenza Vaccine
Effectiveness for Preventing
Laboratory Confirmed Medically
Attended Outcomes’’, Funding
Opportunity Announcement (FOA)
IP08–001 and ‘‘Influenza Vaccine
Efficacy in Tropical and Developing
Countries’’, FOA IP08–002
National Center for Injury Prevention
and Control/ Initial Review Group,
(NCIPC/IRG)
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Clinical Laboratory Improvement
Advisory Committee: Notice of Charter
Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the Clinical
Laboratory Improvement Advisory
Committee, Centers for Disease Control
and Prevention, Department of Health
and Human Services, has been renewed
for a 2-year period through February 19,
2010.
For information, contact Thomas
Hearn, PhD, Executive Secretary,
Clinical Laboratory Improvement
Advisory Committee, Centers for
Disease Control and Prevention,
Department of Health and Human
Services, 1600 Clifton Road, NE.,
Mailstop C12, Atlanta, Georgia 30333,
telephone 404/718–1048 or fax 404/
639–3039.
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 the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: February 29, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–4719 Filed 3–7–08; 8:45 am]
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 aforementioned meeting.
Time and Date: 9 a.m.–5 p.m., April 30,
2008 (Closed).
Place: Centers for Disease Control and
Prevention, Atlanta, GA.
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 Discussed: The meeting will
include the review, discussion, and
evaluation of ‘‘Annual Estimates of Influenza
Vaccine Effectiveness for Preventing
Laboratory Confirmed Medically Attended
Outcomes’’, Funding Opportunity
Announcement (FOA) IP08–001 and
‘‘Influenza Vaccine Efficacy in Tropical and
Developing Countries’’, FOA IP08–002.’’
For Further Information Contact: Christine
J. Morrison, Ph.D., Scientific Review
Administrator, CDC, 1600 Clifton Road, NE.,
Mailstop D72, Atlanta, GA 30333, Telephone:
(404) 639–3098.
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: February 29, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. E8–4754 Filed 3–7–08; 8:45 am]
BILLING CODE 4163–18–P
Times and Dates:
1 p.m.–1:30 p.m., March 26, 2008 (Open)
1:30 p.m.–5 p.m., March 26, 2008 (Closed)
Place: Teleconference.
Status: Portions of the meetings 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 Section
10(d) of Public Law 92–463.
Purpose: This group is charged with
providing advice and guidance to the
Secretary, Department of Health and Human
Services, and the Director, CDC, concerning
the scientific and technical merit of grant and
cooperative agreement applications received
from academic institutions and other public
and private profit and nonprofit
organizations, including State and local
government agencies, to conduct specific
injury research that focuses on prevention
and control.
Matters To Be Discussed: The meeting will
include the review, discussion, and
evaluation of cooperative agreement
applications submitted in response to Fiscal
Year 2008 Requests for Applications related
to the following individual research
announcement: CE08–007, Assessing the
Effects of Interpersonal Violence Prevention
on Suicide.
Agenda items are subject to change as
priorities dictate.
For Further Information Contact: J. Felix
Rogers, Ph.D., M.P.H., Telephone (770) 488–
4334, CDC, 4770 Buford Highway, NE., M/S
F62, Atlanta, Georgia 30341–3724.
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: February 29, 2008.
Elaine L. Baker,
Director, Management Analysis and Services
Office Centers for Disease Control and
Prevention.
[FR Doc. E8–4643 Filed 3–7–08; 8:45 am]
BILLING CODE 4163–18–P
pwalker on PROD1PC71 with NOTICES
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 of the
aforementioned review group:
BILLING CODE 4163–18–P
VerDate Aug<31>2005
16:39 Mar 07, 2008
Jkt 214001
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
E:\FR\FM\10MRN1.SGM
10MRN1
Agencies
[Federal Register Volume 73, Number 47 (Monday, March 10, 2008)]
[Notices]
[Pages 12739-12740]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-4651]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-08-08AS]
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 Acting 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
Surveys of BioSense Trainings,--New--National Center for Public
Health Informatics (NCPHI), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
Congress passed the Public Health Security and Bioterrorism
Preparedness and Response Act of 2002, which requires specific
activities related to bioterrorism preparedness and response. This
congressional mandate outlines the need for improving the overall
public's health through electronic surveillance. The Department of
Health and Human Services outlined strategies aimed at achieving this
goal via the Public Health IT Initiative thereby creating the BioSense
program.
BioSense is the national, human health surveillance system designed
to improve the nation's capabilities for disease detection, monitoring,
and real-time health situational awareness. This work is enhanced by
providing public health real-time access to existing data from
healthcare organizations, state syndromic surveillance systems,
national laboratories, and others for just in time public health
decision-making. BioSense data are analyzed through advanced
statistical methods, and made accessible through the BioSense
application. The application provides data, charts, graphs, and maps
through a secure web-based interface which can be accessed by CDC and
authorized state and local public health and hospital users.
In order to meet the congressional mandate, it is important that
BioSense users understand the role of BioSense in daily surveillance as
well as be able to use specific BioSense modalities to investigate or
monitor any potential disease outbreaks and/or bioterrorist attacks. A
series of training tools have been developed to educate BioSense users
about how best to utilize BioSense in these circumstances.
The training tools were developed based upon a 2007 needs
assessment conducted among BioSense users. Training 1 is an online,
self-paced training module designed for BioSense users at the beginner
level who are not wholly familiar with BioSense or have not used the
system on a regular basis. This module presents the background of
BioSense and an overview of its general functions in a didactic
training style. Training 2 is a virtual training filmed in Second Life.
It is designed for intermediate to advanced level users who are aware
of and have used the general BioSense functionalities for daily
surveillance but want additional skills related to using BioSense
during an emergency scenario. This scenario-based module is presented
in an experiential training style.
Data collection will take place in the form of an online survey
immediately following each training module and a link to an online
survey emailed 3-months post training. This data collection will assess
the goals of these trainings, which are to help registered BioSense
users (1) establish knowledge and efficacy necessary to use BioSense to
investigate and/or monitor a potential event or outbreak; (2)
facilitate communication between BioSense administrators in public
health and hospital settings; (3) access BioSense trainings that are
engaging and easy to use; and (4) use BioSense to investigate and/or
monitor a potential event or outbreak. The post-training and 3-month
follow-up surveys have been pre-tested with less than 9 participants.
Survey results will be used to identify the impact and applicability of
these training modules for BioSense users.
There are no costs to survey respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form Number of responses per per response (in Total burden (in
respondents respondent hours) hours)
----------------------------------------------------------------------------------------------------------------
Post-Training Survey................ 400 1 10/60 67
3-Month Follow Up Survey............ 320 1 5/60 27
---------------------------------------------------------------------------
Total........................... ................. ................. ................. 94
----------------------------------------------------------------------------------------------------------------
[[Page 12740]]
Dated: February 29, 2008.
Maryam I. Daneshvar,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E8-4651 Filed 3-7-08; 8:45 am]
BILLING CODE 4163-18-P