Agency Forms Undergoing Paperwork Reduction Act Review, 83503-83504 [2024-23859]
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Federal Register / Vol. 89, No. 200 / Wednesday, October 16, 2024 / Notices
HMTS include intercept interviews,
telephone interviews, focus groups,
online surveys, and cognitive
interviews. In almost all instances, data
will be collected by outside
organizations under contract with CDC.
For many years, CDC programs have
used HMTS to test and refine message
concepts and test draft materials for
clarity, salience, appeal, and
persuasiveness to target audiences.
Having this Generic Clearance available
has enabled them to test their
information and get critical health
information out to the public quickly.
Over the last three years, more than 27
messages have been tested using this
OMB Clearance package.
CDC’s Division of Tuberculosis
Elimination was approved to conduct
program evaluation for their Latent
Tuberculosis Infection (LTBI)
Awareness Campaign within target
audiences—non-US-born Vietnamese
and Filipino persons and the healthcare
professionals (primary care physicians,
nurse practitioners, and physician
assistants) that serve them. Assessing
the immediate effects of campaign
materials provides helpful insights that
can be used to inform adjustments of
campaign materials for intended
audiences.
CDC’s Division of Nutrition, Physical
Activity, and Obesity (DNPAO) is tasked
with leading our nation’s efforts to
prevent chronic diseases by promoting
good nutrition, regular physical activity,
and a healthy weight. One of the key
ways DNPAO does this is by providing
state and community partners with
practical tools to promote healthy
lifestyles such as the SCHMC
communication resources. It is
imperative that this ad testing be
conducted so that CDC/DNPAO can best
support grantees and local partners by
providing timely information about how
specific ads resonate with key
audiences. The insights gained from the
ad testing also provided DNPAO with
timely information to inform
development of additional ads and
communication materials that they will
resonate with audiences and lead to
intended actions/behavior changes
related to increasing physical activity,
reducing sugary drink consumption,
and improving infant and toddler
nutrition.
83503
The National Center for Injury
Prevention and Control (NCIPC)
collected data to assess older adults’
perceptions of products developed as
part of the expansion phase of CDC’s
Still Going Strong Campaign. Digital
products were developed as part of this
effort to expand the campaign to address
social connectedness and isolation. The
messages conveyed the importance of
social connectedness to health to
maintaining a high quality of life as we
age. Participants learned about how
social connectedness as well as physical
and mental health are interconnected
and critical to the well-being of older
adults.
Over 5,400 burden hours were used
during the previous approval period.
Because the availability of this ICR has
been so critical to programs in
disseminating their materials and
information to the public in a timely
manner, the Office of Communications
is requesting approval for an estimated
2,470 annual burden hours for this
three-year Extension of the information
collection. There is no cost to the
respondents other than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Form name
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Public Health Professionals, Health Care Providers, State and Local Public Health Officials, Emergency Responders, General
Public.
Moderator’s Guides, Eligibility Screeners,
Interview Guides, Opinion Surveys, Consent Forms.
18,525
1
8/60
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–23860 Filed 10–15–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day-25–24GU]
lotter on DSK11XQN23PROD with NOTICES1
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
Adoption and Implementation of the
National Institute of Occupational
VerDate Sep<11>2014
16:43 Oct 15, 2024
Jkt 265001
Safety and Health’s (NIOSH) Outputs’’
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 June 28, 2024, to obtain
comments from the public and affected
agencies. CDC received two nonsubstantive 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
PO 00000
Frm 00058
Fmt 4703
Sfmt 4703
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.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
E:\FR\FM\16OCN1.SGM
16OCN1
83504
Federal Register / Vol. 89, No. 200 / Wednesday, October 16, 2024 / Notices
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. 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 Adoption and
Implementation of the National Institute
of Occupational Safety and Health’s
(NIOSH) Outputs—New—National
Institute of Occupational Safety and
Health’s (NIOSH), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Institute for
Occupational Safety and Health
(NIOSH), is requesting approval of a
new Generic information collection for
a period of three years under the project
titled, ‘‘Assessing Adoption and
Implementation of the National Institute
of Occupational Safety and Health’s
(NIOSH) Outputs.’’
With the continuation of the
Government Performance and Results
Act and the more recent passage of the
Foundations of Evidence-Based Policy
Making Act, there is an increased need
for federal agencies to measure and
demonstrate their impact. However,
measuring impact is challenging,
especially for organizations that have a
science-driven mission because of the
time it takes to move from basic to
applied research. Demonstrating
attribution (cause and effect
relationships) is particularly challenging
for research organizations.
NIOSH research is often designed to
collect implementation and adoption
data through document reviews of
NIOSH records, including grantee final
reports, and through interviews with
NIOSH researchers (federal employees).
While commonly recognized metrics,
these data sources are not
comprehensive, representative, or
informative of the adoption and
implementation of NIOSH products and
efforts. Further, the design and
execution of research projects has
hindered research and program leaders
Type of data
collection
instrument
Type of respondent
Subject matter experts ....................................
Former NIOSH funding recipients ..................
Intermediary or end users (e.g., employers,
workers, manufactures, labor/professional
associations, policymakers).
prioritizing information collections to
understand and assess the adoption and
implementation of research efforts and
products.
The proposed generic information
collection package would allow
researchers to expeditiously pursue
efforts to provide NIOSH with critical
information to inform mission-driven
needs. Additionally, the proposed
efforts go beyond simply measuring
customer satisfaction and rather seek to
advance NIOSH’s burden, need, and
impact framework for future research
while also endeavoring to execute the
Office of Management and Budget’s
(OMB) guidance regarding the
Foundations of Evidence-Based
Policymaking Act.
Respondents are expected to consist
of users and potential users of NIOSH
products including subject matter
expects, former NIOSH funding
recipients, and intermediary and end
users. CDC requests OMB approval for
an estimated 17,150 total burden hours
with an estimated annual burden of
6,069 hours. There is no cost to
respondents other than their time to
participate.
Estimated Annualized Burden Hours
Number of
respondents
Survey instrument (single, pre and post, or
poll) including demographics.
Informed consent form ...................................
Interview or focus group guide ......................
Survey instrument (single, pre and post, or
poll) including demographics.
Informed consent form ...................................
Interview or focus group guide ......................
Survey instrument (single, pre and post, or
poll) including demographics.
[FR Doc. 2024–23859 Filed 10–15–24; 8:45 am]
Food and Drug Administration
[Docket No. FDA–2024–P–4163]
Determination That NOXAFIL
(Posaconazole) Delayed-Release
Tablets, 100 Grams Was Not
Withdrawn From Sale for Reasons of
Safety or Effectiveness
BILLING CODE 4163–18–P
lotter on DSK11XQN23PROD with NOTICES1
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
1
20/60
250
250
200
1
1
1
5/60
1
20/60
25
25
10,000
1
1
1
5/60
1
20/60
650
650
1
1
5/60
1
The Food and Drug
Administration (FDA, Agency, or we)
16:43 Oct 15, 2024
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Frm 00059
Fmt 4703
has determined that NOXAFIL
(posaconazole) delayed-release tablets,
100 grams (g), was not withdrawn from
sale for reasons of safety or
effectiveness. This determination means
that FDA will not begin procedures to
withdraw approval of abbreviated new
drug applications (ANDAs) that refer to
this drug product, and it will allow FDA
to continue to approve ANDAs that refer
to the product as long as they meet
relevant legal and regulatory
requirements.
FOR FURTHER INFORMATION CONTACT:
Notice.
SUMMARY:
VerDate Sep<11>2014
Average
burden per
response
(in hours)
5,000
Informed consent form ...................................
Interview or focus group guide ......................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
Number of
responses per
respondent
Sfmt 4703
Archampong-Gray, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
E:\FR\FM\16OCN1.SGM
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]]>Agencies
[Federal Register Volume 89, Number 200 (Wednesday, October 16, 2024)]
[Notices]
[Pages 83503-83504]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-23859]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-25-24GU]
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 Adoption and Implementation of
the National Institute of Occupational Safety and Health's (NIOSH)
Outputs'' 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 June 28,
2024, to obtain comments from the public and affected agencies. CDC
received two non-substantive 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. Comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
[[Page 83504]]
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function. 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 Adoption and Implementation of the National Institute of
Occupational Safety and Health's (NIOSH) Outputs--New--National
Institute of Occupational Safety and Health's (NIOSH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), National
Institute for Occupational Safety and Health (NIOSH), is requesting
approval of a new Generic information collection for a period of three
years under the project titled, ``Assessing Adoption and Implementation
of the National Institute of Occupational Safety and Health's (NIOSH)
Outputs.''
With the continuation of the Government Performance and Results Act
and the more recent passage of the Foundations of Evidence-Based Policy
Making Act, there is an increased need for federal agencies to measure
and demonstrate their impact. However, measuring impact is challenging,
especially for organizations that have a science-driven mission because
of the time it takes to move from basic to applied research.
Demonstrating attribution (cause and effect relationships) is
particularly challenging for research organizations.
NIOSH research is often designed to collect implementation and
adoption data through document reviews of NIOSH records, including
grantee final reports, and through interviews with NIOSH researchers
(federal employees). While commonly recognized metrics, these data
sources are not comprehensive, representative, or informative of the
adoption and implementation of NIOSH products and efforts. Further, the
design and execution of research projects has hindered research and
program leaders prioritizing information collections to understand and
assess the adoption and implementation of research efforts and
products.
The proposed generic information collection package would allow
researchers to expeditiously pursue efforts to provide NIOSH with
critical information to inform mission-driven needs. Additionally, the
proposed efforts go beyond simply measuring customer satisfaction and
rather seek to advance NIOSH's burden, need, and impact framework for
future research while also endeavoring to execute the Office of
Management and Budget's (OMB) guidance regarding the Foundations of
Evidence-Based Policymaking Act.
Respondents are expected to consist of users and potential users of
NIOSH products including subject matter expects, former NIOSH funding
recipients, and intermediary and end users. CDC requests OMB approval
for an estimated 17,150 total burden hours with an estimated annual
burden of 6,069 hours. There is no cost to respondents other than their
time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Type of data collection Number of Number of burden per
Type of respondent instrument respondents responses per response (in
respondent hours)
----------------------------------------------------------------------------------------------------------------
Subject matter experts................ Survey instrument 5,000 1 20/60
(single, pre and post,
or poll) including
demographics.
Informed consent form... 250 1 5/60
Interview or focus group 250 1 1
guide.
Former NIOSH funding recipients....... Survey instrument 200 1 20/60
(single, pre and post,
or poll) including
demographics.
Informed consent form... 25 1 5/60
Interview or focus group 25 1 1
guide.
Intermediary or end users (e.g., Survey instrument 10,000 1 20/60
employers, workers, manufactures, (single, pre and post,
labor/professional associations, or poll) including
policymakers). demographics.
Informed consent form... 650 1 5/60
Interview or focus group 650 1 1
guide.
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health
Ethics and Regulations, Office of Science, Centers for Disease Control
and Prevention.
[FR Doc. 2024-23859 Filed 10-15-24; 8:45 am]
BILLING CODE 4163-18-P
