Proposed Data Collection Submitted for Public Comment and Recommendations, 4304-4306 [2024-01152]
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4304
Federal Register / Vol. 89, No. 15 / Tuesday, January 23, 2024 / Notices
option to retain historic location data if
it has obtained affirmative express
consent or it ensures that the historic
location data is deidentified or rendered
non-sensitive. Provision XIII requires
Respondent to establish and implement,
and thereafter maintain, a
comprehensive privacy program that
protects the privacy of consumers’
personal information.
Provisions XIV–XVII are reporting
and compliance provisions, which
include recordkeeping requirements and
provisions requiring Respondent to
provide information or documents
necessary for the Commission to
monitor compliance.
Provision XVIII states that the
Proposed Order will remain in effect for
20 years, with certain exceptions.
The purpose of this analysis is to
facilitate public comment on the
Proposed Order, and it is not intended
to constitute an official interpretation of
the complaint or Proposed Order, or to
modify the Proposed Order’s terms in
any way.
By direction of the Commission.
April J. Tabor,
Secretary.
[FR Doc. 2024–01269 Filed 1–22–24; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Board of Scientific Counselors,
National Center for Injury Prevention
and Control; Amended Notice of
Meeting
Centers for Disease Control and
Prevention, Department of Health and
Human Services (HHS).
ACTION: Notice.
AGENCY:
In accordance with the
Federal Advisory Committee Act, the
Centers for Disease Control and
Prevention (CDC) announces an
amendment to the following meeting for
the Board of Scientific Counselors,
National Center for Injury Prevention
and Control (BSC, NCIPC).
SUPPLEMENTARY INFORMATION: Notice is
hereby given of a change in the meeting
of Board of Scientific Counselors,
National Center for Injury Prevention
and Control; January 11, 2024, first
session from 10 a.m. to 12:05 p.m., EST
(OPEN), and second session from 1 p.m.
to 4:30 p.m., EST (CLOSED), in the
original Federal Register notice.
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SUMMARY:
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The notice of the virtual meeting was
published in the Federal Register on
November 17, 2023, 88 FR 80305.
The meeting notice is being amended.
The closed session that was scheduled
for January 11, 2024, from 1 p.m. to 4:30
p.m., EST, has been canceled. The
notice is being amended to update the
SUMMARY, DATES, ADDRESSES, and
SUPPLEMENTARY INFORMATION and should
read as follows:
SUMMARY: In accordance with the
Federal Advisory Committee Act, the
Centers for Disease Control and
Prevention (CDC) announces the
following meeting for the Board of
Scientific Counselors, National Center
for Injury Prevention and Control (BSC,
NCIPC). This meeting is open to the
public. Time will be available for public
comment.
DATES: The meeting will be held on
January 11, 2024, from 10 a.m. to 12:05
p.m., EST. The public comment period
will be from 11:45 a.m. to 12 p.m., EST.
ADDRESSES: Webinar, Atlanta, Georgia.
All participants must register by using
the following link to attend the meeting:
https://cdc.zoomgov.com/meeting/
register/vJItf-igpjopGsXuGUhsdlIOm
RCB2yx509k.
SUPPLEMENTARY INFORMATION:
Purpose: The Board of Scientific
Counselors, National Center for Injury
Prevention and Control (BSC, NCIPC)
will: (1) conduct, encourage, cooperate
with, and assist other appropriate public
health authorities, scientific
institutions, and scientists in the
conduct of research, investigations,
experiments, demonstrations, and
studies relating to the causes and
strategies related to the prevention of
injury, overdose, and violence; (2) assist
States and other entities in preventing
intentional and unintentional injuries,
and to promote health and well-being;
and (3) make recommendations of grants
and cooperative agreements for research
and prevention activities related to
injury, overdose, and violence. The
BSC, NCIPC makes recommendations
regarding policies, strategies, objectives,
and priorities and reviews progress
toward injury, overdose, and violence
prevention. The Board also provides
advice on the appropriate balance of
intramural and extramural research and
provides guidance on the needs,
structure, progress, and performance of
intramural programs. Further, the Board
provides guidance on extramural
scientific program matters.
Additionally, the Board provides
second-level scientific and
programmatic review of applications for
research grants, cooperative agreements,
and training grants related to injury,
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overdose, and violence prevention, and
recommends approval of projects that
merit further consideration for funding
support. The Board also provides
feedback and input on strategic plans,
resources, and priority publications
related to injury, overdose, and violence
prevention.
Matters To Be Considered: The
meeting will include a discussion on the
updated Intimate Partner Violence
Research Priorities. Agenda items are
subject to change as priorities dictate.
FOR FURTHER INFORMATION CONTACT:
Christopher R. Harper, Ph.D.,
Designated Federal Officer, Board of
Scientific Counselors, National Center
for Injury Prevention and Control,
Centers for Disease Control and
Prevention, 4770 Buford Highway NE,
Mailstop S–1069, Atlanta, Georgia
30341. Telephone: (404) 718–8330;
Email: ncipcbsc@cdc.gov.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
Control and Prevention, 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.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2024–01165 Filed 1–22–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day-24–1071; Docket No. CDC–2024–
0002]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a continuing information collection, as
required by the Paperwork Reduction
SUMMARY:
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4305
Federal Register / Vol. 89, No. 15 / Tuesday, January 23, 2024 / Notices
Act of 1995. This notice invites
comment on a proposed information
collection project titled Generic
Clearance for the Collection of
Qualitative Feedback on Agency Service
Delivery. This data collection is
designed to help CDC collect routine
customer feedback on agency service
delivery.
DATES: CDC must receive written
comments on or before March 25, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0002 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to
the address listed above.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 404–639–7570; Email: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. 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;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. 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 submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery (OMB Control No.
0920–1071, Exp. 5/31/2024)—
Extension—National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
CDC/NCEZID is seeking a three-year
Extension of OMB Control No. 0920–
1071 to continue collecting routine
customer feedback on agency service
delivery. Executive Order 12862 directs
Federal agencies to provide service to
the public that matches or exceeds the
best service available in the private
sector. In order to work continuously to
ensure that our programs are effective
and meet our customers’ needs, the
National Center for Emerging and
Zoonotic Infectious Diseases, Centers for
Disease Control and Prevention (CDC)
(hereafter the Agency) seeks to obtain
OMB approval of a Generic Clearance to
collect qualitative feedback on our
service delivery. By qualitative feedback
we mean information that provides
useful insights on perceptions and
opinions, but are not statistical surveys
that yield quantitative results that can
be generalized to the population of
study.
This collection of information is
necessary to enable the Agency to garner
customer and stakeholder feedback in
an efficient, timely manner, in
accordance with our commitment to
improving service delivery. The
information collected from our
customers and stakeholders will help
ensure that users have an effective,
efficient, and satisfying experience with
the Agency’s programs. This feedback
will provide insights into customer or
stakeholder perceptions, experiences
and expectations, provide an early
warning of issues with service, or focus
attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Since getting approval in May 2021,
NCEZID has utilized the 0920–1071
mechanism 15 separate times. In this
Extension, CDC requests OMB approval
for an estimated 3,850 annual burden
hours. There is no cost to respondents
other than the time to participate.
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ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Online surveys ........................................
Focus groups ..........................................
In-person surveys ...................................
Usability testing ......................................
Customer comment cards ......................
1,500
800
1,000
1,500
1,000
1
1
1
1
1
30/60
2
30/60
30/60
15/60
750
1,600
500
750
250
.................................................................
....................
........................
....................
3,850
Form name
General public .........................................
Total .................................................
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Average
burden per
response
(in hours)
Number of
respondents
Type of respondents
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Total
burden
(in hours)
4306
Federal Register / Vol. 89, No. 15 / Tuesday, January 23, 2024 / Notices
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. 2024–01152 Filed 1–22–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Generic Clearance for
Financial Reports Used for ACF
Mandatory Grant Programs (Office of
Management and Budget #: 0970–0510)
Administration for Children
and Families, U.S. Department of Health
and Human Services.
ACTION: Request for public comments.
AGENCY:
The Administration for
Children and Families (ACF) proposes
to extend approval of the existing
overarching generic clearance for
Financial Reports used for ACF
Mandatory Grant Programs (OMB
#0970–0510) as well as all information
collections currently approved under
the overarching generic. There are no
changes to the proposed types of
information collection or uses of data as
described in the overarching generic,
and there are no changes proposed to
currently approved information
collections for which we are requesting
an extension. Burden estimates for the
next 3 years have been adjusted based
on use to date.
DATES: Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing
infocollection@acf.hhs.gov. Identify all
SUMMARY:
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: ACF programs require
detailed financial information from their
grantees that allows ACF to monitor
various specialized cost categories
within each program, to closely manage
program activities, and to have
sufficient financial information to
enable periodic thorough and detailed
audits.
The information included on the
standard Federal Financial Report Form
(SF–425; OMB #4040–0014) provides
only minimal, bare-bones, non-program
specific financial information
insufficient for these purposes. This
generic clearance allows ACF programs
to efficiently develop and receive
approval for financial reports that are
tailored to specific funding recipients
and the associated needs of the program.
This umbrella generic is a mechanism
that is available to all ACF mandatory
grant programs to use to obtain OMB
approval of financial forms. Currently
only a small number of ACF’s
mandatory grant program financial
forms are covered under this umbrella;
it does not cover all ACF mandatory
grant program financial forms. Program
offices use the information collected
under this generic information
collection to:
• Monitor program operations and
prepare technical assistance and
guidance as needed
• Assess the effect of program changes
and make informed decision
• Assist in the computation of the grant
awards issued to each program’s
grantees
• Assist in the computation of the Child
Support Services program’s annual
incentive payments
• Determine that child support
collections are being properly
distributed (Child Support Services
Program only)
• Ensure funding recipients are meeting
funding requirements established by
Congress
• Produce annual financial and
statistical reports as may be required
Number of
respondents
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Study
ACF–196P, TANF Pandemic Emergency Assistance Fund (PEAF) Financial
Report for States, Territories and Tribes .....................................................
Child Care and Development Fund (CCDF) ACF–696 Financial Report for
States and Territories ...................................................................................
Child Care and Development Fund (CCDF) ACF–696T Financial Report for
Tribal Grantees ............................................................................................
Child Support Services Program Financial Reporting Forms (OCSE–34 and
OCSE–396) ..................................................................................................
Form CB–496: Title IV–E Programs Quarterly Financial Report ....................
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by Congress and respond to periodic
detailed inquiries from Congress
ACF may require an information
collection approved under this generic
from funding recipients to obtain or
retain benefits.
Prior to a new form being submitted
for review under this umbrella generic,
ACF will publish a notice in the Federal
Register announcing the agency’s
intention to request an OMB review of
the form and providing a 14-day period
for public comment on that specific
request. ACF will review any comments
received and address them as
appropriate. ACF will provide a copy of
any comments received and will
provide a description of how comments
were considered in the submission form
along with the request package for the
individual collection. ACF will then
follow standard OMB requirements for a
generic information collection and
submit a generic information collection
request for each individual data
collection activity under this generic
clearance. Each request will include the
individual form(s) and instructions, a
summary of any comments received,
and a short overview of the proposed
purpose and use of the data collected.
OMB should review requests within 10
days of submission.
Respondents: ACF-funded mandatory
grant programs.
Annual Burden Estimates
Find currently approved information
collections here: https://
www.reginfo.gov/public/do/PRAICList?
ref_nbr=202308-0970-008. The request
to OMB will include an extension
request for approved information
collections that are planned to continue
beyond spring 2024. The current list of
ongoing collections follows, but more
collections may be approved prior to
submission of the extension request to
OMB. We will update the list in the
subsequent Federal Register notice, if
needed.
Burden Estimates—Ongoing Requests
Number of
responses per
respondent
Average
burden hours
per response
Burden hours
137
1
6
822
56
4
5
1,120
221
1
7
1,547
168
67
4
4
14
25
9,408
6,700
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23JAN1
]]>Agencies
[Federal Register Volume 89, Number 15 (Tuesday, January 23, 2024)]
[Notices]
[Pages 4304-4306]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-01152]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-1071; Docket No. CDC-2024-0002]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a continuing information
collection, as required by the Paperwork Reduction
[[Page 4305]]
Act of 1995. This notice invites comment on a proposed information
collection project titled Generic Clearance for the Collection of
Qualitative Feedback on Agency Service Delivery. This data collection
is designed to help CDC collect routine customer feedback on agency
service delivery.
DATES: CDC must receive written comments on or before March 25, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0002 by either of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.regulations.gov) or by U.S. mail to the address listed
above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570;
Email: [email protected].
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each collection of
information they conduct or sponsor. In addition, the PRA also requires
Federal agencies to provide a 60-day notice in the Federal Register
concerning each proposed collection of information, including each new
proposed collection, each proposed extension of existing collection of
information, and each reinstatement of previously approved information
collection before submitting the collection to the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. 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;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. 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
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Generic Clearance for the Collection of Qualitative Feedback on
Agency Service Delivery (OMB Control No. 0920-1071, Exp. 5/31/2024)--
Extension--National Center for Emerging and Zoonotic Infectious
Diseases (NCEZID), Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC/NCEZID is seeking a three-year Extension of OMB Control No.
0920-1071 to continue collecting routine customer feedback on agency
service delivery. Executive Order 12862 directs Federal agencies to
provide service to the public that matches or exceeds the best service
available in the private sector. In order to work continuously to
ensure that our programs are effective and meet our customers' needs,
the National Center for Emerging and Zoonotic Infectious Diseases,
Centers for Disease Control and Prevention (CDC) (hereafter the Agency)
seeks to obtain OMB approval of a Generic Clearance to collect
qualitative feedback on our service delivery. By qualitative feedback
we mean information that provides useful insights on perceptions and
opinions, but are not statistical surveys that yield quantitative
results that can be generalized to the population of study.
This collection of information is necessary to enable the Agency to
garner customer and stakeholder feedback in an efficient, timely
manner, in accordance with our commitment to improving service
delivery. The information collected from our customers and stakeholders
will help ensure that users have an effective, efficient, and
satisfying experience with the Agency's programs. This feedback will
provide insights into customer or stakeholder perceptions, experiences
and expectations, provide an early warning of issues with service, or
focus attention on areas where communication, training or changes in
operations might improve delivery of products or services. These
collections will allow for ongoing, collaborative and actionable
communications between the Agency and its customers and stakeholders.
It will also allow feedback to contribute directly to the improvement
of program management.
Since getting approval in May 2021, NCEZID has utilized the 0920-
1071 mechanism 15 separate times. In this Extension, CDC requests OMB
approval for an estimated 3,850 annual burden hours. There is no cost
to respondents other than the time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total
Type of respondents Form name respondents responses per response burden (in
respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
General public.................... Online surveys....... 1,500 1 30/60 750
Focus groups......... 800 1 2 1,600
In-person surveys.... 1,000 1 30/60 500
Usability testing.... 1,500 1 30/60 750
Customer comment 1,000 1 15/60 250
cards.
------------------------------------------------------
Total......................... ..................... ........... .............. ........... 3,850
----------------------------------------------------------------------------------------------------------------
[[Page 4306]]
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. 2024-01152 Filed 1-22-24; 8:45 am]
BILLING CODE 4163-18-P
