Agency Forms Undergoing Paperwork Reduction Act Review, 30120-30121 [2019-13519]
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30120
Federal Register / Vol. 84, No. 123 / Wednesday, June 26, 2019 / Notices
active and a cluster close-out form when
cluster response activities are closed or
at annual intervals while a cluster
response remains active. Completion of
forms will be determined by the number
of clusters detected. Health departments
that do not identify recent and rapid
clusters of HIV transmission will not
complete any cluster report forms, while
some jurisdictions will detect multiple
recent and rapid clusters of HIV
transmission, necessitating the
completion of multiple cluster report
forms. CDC estimates on average health
departments will provide information
for 2.5 initial cluster reports, five
Cluster Follow-up reports, and 2.5
Cluster Close-out reports annually.
Perinatal HIV surveillance and
prevention activities with HIV exposure
reporting and perinatal services
coordination is an integrated approach
to advancing the progress toward
perinatal HIV elimination goals. A
subset of 16 health departments in the
most affected jurisdictions will be
reporting using the Perinatal Exposure
Reporting (PHER) form to monitor and
evaluate perinatal HIV prevention
efforts. An estimated 197 reports
containing perinatal exposure data
elements will be processed on average
annually by each of the 16 health
departments reporting data collected as
part of PHER. These supplemental data
are also reported monthly to CDC.
The Standards Evaluation Report
(SER) is used by CDC and Health
Departments to improve data quality,
interpretation, usefulness, and
surveillance system efficiency, as well
as to monitor progress toward meeting
surveillance program objectives. The
information collected for the SER
includes a brief set of questions about
evaluation outcomes and the collection
of laboratory data that will be reported
one time a year by each 59 health
departments. The total estimated annual
burden hours are 58,131.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents
Health
Health
Health
Health
Health
Health
Health
Health
Health
Health
Health
Health
Departments
Departments
Departments
Departments
Departments
Departments
Departments
Departments
Departments
Departments
Departments
Departments
........................................
........................................
........................................
........................................
........................................
........................................
........................................
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........................................
........................................
........................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–13521 Filed 6–25–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–19–18AMQ]
jbell on DSK3GLQ082PROD 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 Assessing
impact of the NIOSH research 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 July 20, 2018 to obtain
comments from the public and affected
VerDate Sep<11>2014
18:47 Jun 25, 2019
Number of
respondents
Form name
Jkt 247001
Adult HIV Case Report ..................................
Pediatric HIV Case Report .............................
Case Report Evaluations ...............................
Case Report Updates ....................................
Laboratory Updates ........................................
Deduplication Activities ..................................
Investigation Reporting and Evaluation .........
Initial Cluster Report Form .............................
Cluster Follow-up Form ..................................
Cluster Close-out Form ..................................
Perinatal HIV Exposure Reporting (PHER) ...
Annual Reporting: Standards Evaluation Report (SER).
agencies. CDC received two 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
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
59
59
59
59
59
59
59
59
59
59
16
59
Number of
responses per
respondent
854
3
86
2,353
9,410
2,741
901
2.5
5
2.5
197
1
Average
burden per
response
(in hours)
20/60
20/60
20/60
2/60
0.5/60
10/60
1/60
1
30/60
1
30/60
8
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
Assessing impact of the NIOSH
research—New—National Institute for
Occupational Safety and Health
(NIOSH), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The National Institute for
Occupational Safety and Health
(NIOSH) is responsible for conducting
research and making recommendations
E:\FR\FM\26JNN1.SGM
26JNN1
30121
Federal Register / Vol. 84, No. 123 / Wednesday, June 26, 2019 / Notices
to prevent worker injury and illness, as
authorized in Section 20(a)(1) of the
Occupational Safety and Health Act (29
U.S.C. 669). NIOSH is strongly
committed to program evaluation as a
way to maximize its contributions to
improved occupational safety and
health. NIOSH is requesting a new
generic information collection request
for a three-year period that will support
the timely information collection
needed for upcoming program
evaluation activities, such as external
reviews of NIOSH research programs
(which fulfil a Government Performance
and Results Act (GPRA) requirement),
studies to understand the economic
value of NIOSH research, process
evaluations of NIOSH programs, and
evaluations of large research projects.
For these reviews, NIOSH needs to
collect information about research
dissemination and achieved outcomes
from key audiences (grantees, potential
NIOSH research users and relevant
safety and health experts) for
accountability and program
improvement purposes. NIOSH is
specifically interested in assessing
intermediate outcomes — the use of
NIOSH research products and findings
by external stakeholders and partners to
improve safety and health — as
evidence of research impact. Being able
to collect information on intermediate
outcomes from grantees, as well as past,
present, and potential future users of
NIOSH research would allow us to
provide more robust evidence of use or
adoption of NIOSH research products or
findings.
The evaluation findings and
recommendations from the various
program evaluation activities described
above will be used as an input for future
direction of the programs and
incorporated into analyses and reports
to either investigate the value of
NIOSH’s research, or improve program
operations to maximize impact.
Data will be collected through semistructured key informant interviews
with grantees, potential or known users
of NIOSH research, and subject matter
experts in safety and health. NIOSH
estimates that 30 respondents will be
involved in phone interviews, which
would last between 30–60 minutes.
However, participants might be
burdened an additional hour reading the
invitation email and providing relevant
documents such as evidence of research
impact. Therefore, the estimated burden
for each participant is two hours. The
total estimated burden is 60 hours.
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Natural science managers ..............................
Semi-Structured Interview Guide (Subject
Matter Experts).
Semi-Structured Interview Guide (Grantees)
Semi-Structured Interview Guide (Research
users).
Postsecondary Teachers ................................
Industrial production managers ......................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2019–13519 Filed 6–25–19; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–19–0009]
Agency Forms Undergoing Paperwork
Reduction Act Review
jbell on DSK3GLQ082PROD 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 National
Disease Surveillance Program—I. Case
Reports 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 April 8,
2019 to obtain comments from the
public and affected agencies. CDC did
not receive comments related to the
VerDate Sep<11>2014
18:47 Jun 25, 2019
Jkt 247001
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.
PO 00000
Frm 00040
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
Average
burden per
response
(in hours)
10
1
2
12
8
1
1
2
2
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
National Disease Surveillance
Program—I. Case Reports (0920–0009,
Exp. 6/30/2019)—Extension—National
Center for Emerging and Zoonotic
Infectious Diseases (NCEZID), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
Surveillance of the incidence and
distribution of disease has been an
important function of the US Public
Health Service (PHS) since an 1878 Act
of Congress authorized the PHS to
collect morbidity reports. After the
Malaria Control in War Areas Program
had fulfilled its original 1942 objective
of reducing malaria transmission, its
E:\FR\FM\26JNN1.SGM
26JNN1
]]>Agencies
[Federal Register Volume 84, Number 123 (Wednesday, June 26, 2019)]
[Notices]
[Pages 30120-30121]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-13519]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-19-18AMQ]
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 Assessing impact of the NIOSH research 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 July 20, 2018 to obtain
comments from the public and affected agencies. CDC received two
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
Assessing impact of the NIOSH research--New--National Institute for
Occupational Safety and Health (NIOSH), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The National Institute for Occupational Safety and Health (NIOSH)
is responsible for conducting research and making recommendations
[[Page 30121]]
to prevent worker injury and illness, as authorized in Section 20(a)(1)
of the Occupational Safety and Health Act (29 U.S.C. 669). NIOSH is
strongly committed to program evaluation as a way to maximize its
contributions to improved occupational safety and health. NIOSH is
requesting a new generic information collection request for a three-
year period that will support the timely information collection needed
for upcoming program evaluation activities, such as external reviews of
NIOSH research programs (which fulfil a Government Performance and
Results Act (GPRA) requirement), studies to understand the economic
value of NIOSH research, process evaluations of NIOSH programs, and
evaluations of large research projects. For these reviews, NIOSH needs
to collect information about research dissemination and achieved
outcomes from key audiences (grantees, potential NIOSH research users
and relevant safety and health experts) for accountability and program
improvement purposes. NIOSH is specifically interested in assessing
intermediate outcomes -- the use of NIOSH research products and
findings by external stakeholders and partners to improve safety and
health -- as evidence of research impact. Being able to collect
information on intermediate outcomes from grantees, as well as past,
present, and potential future users of NIOSH research would allow us to
provide more robust evidence of use or adoption of NIOSH research
products or findings.
The evaluation findings and recommendations from the various
program evaluation activities described above will be used as an input
for future direction of the programs and incorporated into analyses and
reports to either investigate the value of NIOSH's research, or improve
program operations to maximize impact.
Data will be collected through semi-structured key informant
interviews with grantees, potential or known users of NIOSH research,
and subject matter experts in safety and health. NIOSH estimates that
30 respondents will be involved in phone interviews, which would last
between 30-60 minutes. However, participants might be burdened an
additional hour reading the invitation email and providing relevant
documents such as evidence of research impact. Therefore, the estimated
burden for each participant is two hours. The total estimated burden is
60 hours.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Natural science managers.............. Semi-Structured 10 1 2
Interview Guide
(Subject Matter
Experts).
Postsecondary Teachers................ Semi-Structured 12 1 2
Interview Guide
(Grantees).
Industrial production managers........ Semi-Structured 8 1 2
Interview Guide
(Research users).
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2019-13519 Filed 6-25-19; 8:45 am]
BILLING CODE 4163-18-P
