Agency Forms Undergoing Paperwork Reduction Act Review, 66908-66909 [2019-26368]
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Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
consultants such as survey
methodologist, academic researchers,
clinicians or other health care providers;
NHANES data or website users;
members of the general public or
individuals abroad who would be part
of a collaborative development project
or projects between NCHS and related
public health agencies in the U.S. and/
or abroad. The type of participant
involved in a given developmental
project would be determined by the
nature of the project. The details of each
project will be included in the specific
GenIC submissions.
There is no cost to respondents other
than their time. A three-year clearance
is requested. The estimated annualized
burden hours for this generic data
collection is 59,465.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses
per
respondent
Average
burden per
response
(in hours)
Total
burden
(in hours)
Form name
Individuals or Households .................
Developmental Projects & Focus
Group documents.
Developmental Projects & Focus
Group documents.
24-hour developmental projects .......
35,000
1
1.5
52,500
300
1
1.5
450
200
1
25
5,000
Developmental Projects ...................
Focus Group/Developmental Project
Documents.
1,000
15
1
1
1.5
1
1,500
15
...........................................................
........................
........................
........................
59,465
Volunteers .........................................
Individuals or households, Volunteers, NHANES Participants.
NHANES participants ........................
Subject Matter Experts .....................
Total ...........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–26374 Filed 12–5–19; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–1011]
Agency Forms Undergoing Paperwork
Reduction Act Review
lotter on DSKBCFDHB2PROD with NOTICES
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled Emergency
Epidemic Investigation Data Collections
(OMB control number 0920–1011), for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on
September 4, 2019 to obtain comments
from the public and affected agencies.
CDC did not receive comments related
to the previous notice. This notice
serves to allow an additional 30 days for
public and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
VerDate Sep<11>2014
16:11 Dec 05, 2019
Jkt 250001
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
Emergency Epidemic Investigation
Data Collections (OMB Control No.
0920–1011, Exp. 01/31/2020)—
Extension—Center for Surveillance,
Education, and Laboratory Services
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
(CSELS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC previously conducted Emergency
Epidemic Investigations (EEIs) under
Office of Management and Budget
(OMB) Control Number 0920–0008. In
2013, CDC received OMB approval
(OMB Control Number 0920–1011) for a
new OMB generic clearance for a threeyear period to collect vital information
during EEIs in response to urgent
outbreaks or events (i.e., natural,
biological, chemical, nuclear,
radiological) characterized by
undetermined agents, undetermined
sources, undetermined transmission, or
undetermined risk factors. This generic
clearance was approved for a three-year
extension, which expires on 1/31/2020.
CDC seeks OMB approval for an
extension of this generic clearance for
an additional three-year period.
Supporting effective emergency
epidemic investigations is one of the
most important ways that CDC protects
the health of the public. CDC is
frequently called upon to conduct EEIs
at the request of local, state, or
international health authorities seeking
support to respond to urgent outbreaks
or urgent public health-related events.
In response to external partner requests,
CDC provides necessary epidemiologic
support to identify the agents, sources,
modes of transmission, or risk factors to
effectively implement rapid prevention
and control measures to protect the
public’s health. Data collection is a
critical component of the epidemiologic
support provided by CDC; data are
E:\FR\FM\06DEN1.SGM
06DEN1
66909
Federal Register / Vol. 84, No. 235 / Friday, December 6, 2019 / Notices
analyzed to determine the agents,
sources, modes of transmission, or risk
factors so that effective prevention and
control measures can be implemented.
During an unanticipated outbreak or
event, immediate action by CDC is
necessary to minimize or prevent public
harm. The legal justification for EEIs are
found in the Public Health Service Act
(42 U.S.C. Sec. 301 [241]) (a).
Successful investigations are
dependent on rapid and flexible data
collection that evolves during the
investigation and is customized to the
unique circumstances of each outbreak
or event. Data collection elements will
be those necessary to identify the
agents, sources, mode of transmission,
or risk factors. Examples of potential
data collection methods include
telephone or face-to-face interview;
email, web or other type of electronic
questionnaire; paper-and-pencil
questionnaire; focus groups; medical
record review; laboratory record review;
collection of clinical samples; and
environmental assessment. Respondents
will vary depending on the nature of the
outbreak or event; examples of potential
respondents include health care
professionals, patients, laboratorians,
and the general public. Participation in
EEIs is voluntary and there are no
anticipated costs to respondents other
than their time. CDC will use the
information gathered during EEIs to
rapidly identify and effectively
implement measures to minimize or
prevent public harm.
CDC projects 60 EEIs in response to
outbreaks or events characterized by
undetermined agents, undetermined
sources, undetermined transmission, or
undetermined risk factors annually. The
projected average number of
respondents is 200 per EEI, for a total
of 12,000 respondents. CDC estimates
the average burden per response is 0.5
hours and each respondent will be
asked to respond once. Therefore, the
total estimated annual burden hours are
6,000. These estimates are based on the
reported burden for EEIs that have been
performed during the previous two
years. OMB approval is requested for
three years.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Emergency Epidemic Investigation Participants.
Emergency Epidemic Investigation Data Collection Instruments.
12,000
1
30/60
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–26368 Filed 12–5–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–20–1154]
lotter on DSKBCFDHB2PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled CDC/ATSDR
Formative Research and Tool
Development to the Office of
Management and Budget (OMB) for
review and approval. CDC previously
published a ‘‘Proposed Data Collection
Submitted for Public Comment and
Recommendations’’ notice on August
23, 2019 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
previous notice. This notice serves to
allow an additional 30 days for public
and affected agency comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
VerDate Sep<11>2014
16:11 Dec 05, 2019
Jkt 250001
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570 or
send an email to omb@cdc.gov. Direct
written comments and/or suggestions
regarding the items contained in this
notice to the Attention: CDC Desk
Officer, Office of Management and
Budget, 725 17th Street NW,
Washington, DC 20503 or by fax to (202)
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
395–5806. Provide written comments
within 30 days of notice publication.
Proposed Project
CDC/ATSDR Formative Research and
Tool Development—(OMB Control No.
0920–1154, Exp. 1/31/2020)—
Extension—Office of Science (OS),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) requests approval for
an extension of a generic clearance for
CDC/ATSDR Formative Research and
Tool Development. This information
collection request is designed to allow
CDC to conduct formative research
information collection activities used to
inform many aspects of surveillance,
communications, health promotion, and
research project development at CDC.
Formative research is the basis for
developing effective strategies including
communication channels, for
influencing behavior change. It helps
researchers identify and understand the
characteristics—interests, behaviors and
needs—of target populations that
influence their decisions and actions.
Formative research is integral in
developing programs as well as
improving existing and ongoing
programs. Formative research looks at
the community in which a public health
intervention is being or will be
implemented and helps the project staff
E:\FR\FM\06DEN1.SGM
06DEN1
Agencies
[Federal Register Volume 84, Number 235 (Friday, December 6, 2019)]
[Notices]
[Pages 66908-66909]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-26368]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-20-1011]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled Emergency Epidemic Investigation Data
Collections (OMB control number 0920-1011), for review and approval.
CDC previously published a ``Proposed Data Collection Submitted for
Public Comment and Recommendations'' notice on September 4, 2019 to
obtain comments from the public and affected agencies. CDC did not
receive comments related to the previous notice. This notice serves to
allow an additional 30 days for public and affected agency comments.
CDC will accept all comments for this proposed information
collection project. The Office of Management and Budget is particularly
interested in comments that:
(a) Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
(b) Evaluate the accuracy of the agencies estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and clarity of the information to
be collected;
(d) Minimize the burden of the collection of information on those
who are to respond, including, through the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology, e.g., permitting
electronic submission of responses; and
(e) Assess information collection costs.
To request additional information on the proposed project or to
obtain a copy of the information collection plan and instruments, call
(404) 639-7570 or send an email to [email protected]. Direct written comments
and/or suggestions regarding the items contained in this notice to the
Attention: CDC Desk Officer, Office of Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by fax to (202) 395-5806. Provide
written comments within 30 days of notice publication.
Proposed Project
Emergency Epidemic Investigation Data Collections (OMB Control No.
0920-1011, Exp. 01/31/2020)--Extension--Center for Surveillance,
Education, and Laboratory Services (CSELS), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
CDC previously conducted Emergency Epidemic Investigations (EEIs)
under Office of Management and Budget (OMB) Control Number 0920-0008.
In 2013, CDC received OMB approval (OMB Control Number 0920-1011) for a
new OMB generic clearance for a three-year period to collect vital
information during EEIs in response to urgent outbreaks or events
(i.e., natural, biological, chemical, nuclear, radiological)
characterized by undetermined agents, undetermined sources,
undetermined transmission, or undetermined risk factors. This generic
clearance was approved for a three-year extension, which expires on 1/
31/2020. CDC seeks OMB approval for an extension of this generic
clearance for an additional three-year period.
Supporting effective emergency epidemic investigations is one of
the most important ways that CDC protects the health of the public. CDC
is frequently called upon to conduct EEIs at the request of local,
state, or international health authorities seeking support to respond
to urgent outbreaks or urgent public health-related events. In response
to external partner requests, CDC provides necessary epidemiologic
support to identify the agents, sources, modes of transmission, or risk
factors to effectively implement rapid prevention and control measures
to protect the public's health. Data collection is a critical component
of the epidemiologic support provided by CDC; data are
[[Page 66909]]
analyzed to determine the agents, sources, modes of transmission, or
risk factors so that effective prevention and control measures can be
implemented. During an unanticipated outbreak or event, immediate
action by CDC is necessary to minimize or prevent public harm. The
legal justification for EEIs are found in the Public Health Service Act
(42 U.S.C. Sec. 301 [241]) (a).
Successful investigations are dependent on rapid and flexible data
collection that evolves during the investigation and is customized to
the unique circumstances of each outbreak or event. Data collection
elements will be those necessary to identify the agents, sources, mode
of transmission, or risk factors. Examples of potential data collection
methods include telephone or face-to-face interview; email, web or
other type of electronic questionnaire; paper-and-pencil questionnaire;
focus groups; medical record review; laboratory record review;
collection of clinical samples; and environmental assessment.
Respondents will vary depending on the nature of the outbreak or event;
examples of potential respondents include health care professionals,
patients, laboratorians, and the general public. Participation in EEIs
is voluntary and there are no anticipated costs to respondents other
than their time. CDC will use the information gathered during EEIs to
rapidly identify and effectively implement measures to minimize or
prevent public harm.
CDC projects 60 EEIs in response to outbreaks or events
characterized by undetermined agents, undetermined sources,
undetermined transmission, or undetermined risk factors annually. The
projected average number of respondents is 200 per EEI, for a total of
12,000 respondents. CDC estimates the average burden per response is
0.5 hours and each respondent will be asked to respond once. Therefore,
the total estimated annual burden hours are 6,000. These estimates are
based on the reported burden for EEIs that have been performed during
the previous two years. OMB approval is requested for three years.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Emergency Epidemic Investigation Emergency Epidemic 12,000 1 30/60
Participants. Investigation Data
Collection Instruments.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-26368 Filed 12-5-19; 8:45 am]
BILLING CODE 4163-18-P