Agency Information Collection Activities: Proposed Collection; Comment Request, 64795-64797 [2022-23334]
Download as PDF
<![CDATA[
64795
Federal Register / Vol. 87, No. 206 / Wednesday, October 26, 2022 / Notices
State
Nebraska ............................
Ohio ....................................
Oklahoma ...........................
Texas .................................
City
Address
Waynesville ........................
Beatrice ..............................
Gothenburg ........................
Grand Island ......................
Hastings .............................
Kearney ..............................
Lexington ...........................
Lincoln ................................
McCook ..............................
Nebraska City ....................
110 C W Parker Lane, Waynesville, Missouri 65583 ....
2415 North 6th Street, Beatrice, Nebraska 68310 ........
716 4th Street, Gothenburg, Nebraska 69138 ...............
515 South Webb Road, Grand Island, Nebraska 68803
1315 West J Street, Hastings, Nebraska 68901 ...........
910 Third Avenue, Kearney, Nebraska 68845 ..............
1701 Plumcreek Parkway, Lexington, Nebraska 68850
5640 Cornhusker Highway, Lincoln, Nebraska 68507 ..
1602 North Highway 83, McCook, Nebraska 69001 .....
2412 South 11th Street, Nebraska City, Nebraska
68410.
2501 East 4th Street, North Platte, Nebraska 69101 ....
518 S Lincoln Avenue, York, Nebraska 68467 ..............
206 Sterling Run Blvd., Mount Orab, Ohio 45154 .........
724 Arlington Center, Ada, Oklahoma 74820 ................
1925 N Rockford Road, Ardmore, Oklahoma 73401 .....
4800 N Highway 81, Duncan, Oklahoma 73533 ...........
2424 West Main Street, Durant, Oklahoma 74701 ........
6 East Shawnee Road, Muskogee, Oklahoma 74403 ...
329 South Ash Street, Nowata, Oklahoma 74048 .........
2000 South Wood Drive, Okmulgee, Oklahoma 74447
715 North Mill Street, Pryor, Oklahoma 74361 ..............
1200 W U.S. Business Hwy. 380, Decatur, Texas
76234.
2725 Hwy. 75 North, Sherman, Texas 75090 ...............
2701 S Jack Kultgen Expressway, Waco, Texas 76706
102 College Park Drive, Weatherford, Texas 76086 .....
North Platte ........................
York ....................................
Mount Orab ........................
Ada .....................................
Ardmore .............................
Duncan ...............................
Durant ................................
Muskogee ..........................
Nowata ...............................
Okmulgee ...........................
Pryor ..................................
Decatur ..............................
Sherman ............................
Waco ..................................
Weatherford .......................
The purpose of this analysis is to
facilitate public comment on the
Consent Agreement. It is not intended to
constitute an official interpretation of
the Consent Agreement or to modify its
terms in any way.
By direction of the Commission.
April J. Tabor,
Secretary.
[FR Doc. 2022–23245 Filed 10–25–22; 8:45 am]
BILLING CODE 6750–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Proposed Project
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) re-approve the proposed
information collection project ‘‘The
Systematic Review Data Repository
(SRDR) Platform’’. This proposed
information collection was previously
published in the Federal Register on
August 12, 2022 and allowed 60 days
for public comment. AHRQ did not
receive substantive comments during
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:37 Oct 25, 2022
Jkt 259001
public review period. The purpose of
this notice is to allow an additional 30
days for public comment.
DATES: Comments on this notice must be
received by November 25, 2022.
ADDRESSES: Written 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
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
email at doris.lefkowitz@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
‘‘The Systematic Review Data
Repository (SRDR) Platform’’
Since 1997, the AHRQ Evidencebased Practice Center (EPC) Program has
been reviewing relevant scientific
information on a wide spectrum of
clinical and health services topics to
produce various types of evidence
reports. A majority of these evidence
reports are systematic reviews (SRs),
which are used as evidence bases for
clinical practice guidelines, research
agendas, healthcare coverage, and other
health related policies. Performing SRs
is costly in time, labor, and money.
Moreover, there is an increasing
expectation of quicker turnaround in
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
Store No.
Buyer
24
95
101
115
42
25
100
63
70
67
Bomgaars.
Buchheit.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
102
27
173
22
86
85
83
56
156
23
54
178
Buchheit.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
Bomgaars.
175
177
176
Bomgaars.
Bomgaars.
Bomgaars.
producing SRs to accommodate the fast
moving pace of innovations and new
scientific discoveries in healthcare.
Some SRs overlap or are duplicated;
independent teams of SR producers
often extract data from the same studies,
resulting in replication of work. Current
methodology makes it difficult to
harness and reuse previous work when
updating SRs.
In an effort to reduce the economic
burden of conducting SRs, the EPC
program undertook development of a
collaborative, Web-based repository of
systematic review data called the
Systematic Review Data Repository
(SRDR). The OMB Control Number for
this data collection is 0935–0244, which
was last approved by OMB on October
16, 2019.
This resource serves as both an
archive and data extraction tool, shared
among organizations and individuals
producing SRs worldwide, enabling the
creation of a central database of SR data.
This database is collaboratively vetted,
freely accessible, and integrates
seamlessly with reviewers’ existing
workflows, with the ultimate goal of
facilitating the efficient generation and
update of evidence reviews, and thus
speeding and improving evidence-based
policy-making with regards to health
care.
Note that the SRDR system was
upgraded during the last period of OMB
clearance and is now designated as
SRDR+. We will use the term ‘‘SRDR
platform’’ to collectively denote the
E:\FR\FM\26OCN1.SGM
26OCN1
64796
Federal Register / Vol. 87, No. 206 / Wednesday, October 26, 2022 / Notices
various upgraded iterations of the
platform.
The SRDR project aims to achieve the
following goals:
(1) Create online easy-to-use Webbased tools for conducting systematic
reviews to facilitate extraction of data
from primary studies;
(2) Develop an open-access searchable
archive of key questions addressed in
systematic reviews;
(3) Maintain a public repository of
primary study data including provision
of technical support for repository users;
and
(4) Develop a process for making
summary data from systematic reviews
digitally shareable to end-users.
This study is being conducted by
AHRQ through its contractor, Brown
University, pursuant to AHRQ’s
statutory authority to conduct and
support research on healthcare and on
systems for the delivery of such care,
including activities with respect to the
quality, effectiveness, efficiency,
appropriateness and value of healthcare
services, including database
development. 42 U.S.C. 299a(a)(1) and
(8).
Method of Collection
To achieve the goals of this project the
following data collections are being
implemented:
(1) Collect registration information on
SRs from SR producers who will
populate the SRDR platform.
The SRDR platform now uses a twotiered categorization of users, and
collection of registration data will
depend on the type of user.
‘‘Contributors’’ are SR producers who
use the SRDR platform as a tool to
support production of the SR and share
scientific data from their SRs.
Registration data will be collected from
these users. ‘‘General public’’ users only
view scientific data publicly available in
the SRDR platform. No data will be
collected from these users. The
‘‘Commentator’’ category of users that
were referenced in the last OMB
clearance period has been eliminated in
the updated system since no users have
signed up to be commentators. All
Contributors undergo a simple selfregistration process by providing a
password and an email address.
Provision of username and institution
information by registrants is now
optional in the updated system.
Collection of registration data from
Contributors is required due to the
technical nature of using the SRDR
platform both as a database and a tool
for assisting in the production of a SR,
including providing comments in the
various sections of a particular project
on the SRDR platform. In addition,
provision of an email address and
institution information allows the
administrators of the SRDR platform to
confirm that requests are being made by
actual people and not potentially
malicious software code such as bots
and other cybersecurity threats.
User registration will be used for
administrative purposes only including
communication between SRDR platform
administrators and registrant users. This
type of information will not be made
publicly available.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondents’ time to participate/use the
SRDR platform. In 2020, 1,029 users
registered as Contributors. Registration
will take approximately 1.5 minutes or
0.025 hours per user. We thus calculate
the total burden hours required for
registration for all users annually is
25.73 hours.
EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Hours per
response
Total burden
hours
Registration of users as Contributors ..............................................................
1,029
1
0.025
25.73
Total ..........................................................................................................
1,029
........................
........................
25.73
Exhibit 2 shows the estimated cost
burden associated with the respondents’
time to participate/use the SRDR
platform. The total cost burden to
respondents is estimated at an average
of $1,126.97 annually.
EXHIBIT 2—ESTIMATED ANNUALIZED COST BURDEN
Number of
respondents
Form name
Total burden
hours
Average
hourly wage
rate *
Total cost
burden
Registration of users as Commentators or Contributors .................................
1,029
25.73
a $43.80
$1,126.97
Total ..........................................................................................................
1,029
25.73
........................
1,126.97
* National Compensation Survey: Occupational wages in the United States May 2021, ‘‘U.S. Department of Labor, Bureau of Labor Statistics.’’
Available at: https://www.bls.gov/oes/current/oes290000.htm.
a Based on the mean wages for Healthcare Practitioners and Technical Occupations, 29–0000.
lotter on DSK11XQN23PROD with NOTICES1
Request for Comments
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
comments on AHRQ’s information
collection are requested with regard to
any of the following: (a) whether the
proposed collection of information is
necessary for the proper performance of
AHRQ’s health care research and health
VerDate Sep<11>2014
17:37 Oct 25, 2022
Jkt 259001
care information dissemination
functions, including whether the
information will have practical utility;
(b) the accuracy of AHRQ’s estimate of
burden (including hours and costs) of
the proposed collection(s) of
information; (c) ways to enhance the
quality, utility and clarity of the
information to be collected; and (d)
PO 00000
Frm 00043
Fmt 4703
Sfmt 4703
ways to minimize the burden of the
collection of information upon the
respondents, including the use of
automated collection techniques or
other forms of information technology.
Comments submitted in response to
this notice will be summarized and
included in the Agency’s subsequent
request for OMB approval of the
E:\FR\FM\26OCN1.SGM
26OCN1
64797
Federal Register / Vol. 87, No. 206 / Wednesday, October 26, 2022 / Notices
proposed information collection. All
comments will become a matter of
public record.
Dated: October 21, 2022.
Marquita Cullom,
Associate Director.
[FR Doc. 2022–23334 Filed 10–25–22; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Expedited Review and Public
Comment: Monitoring and Compliance
for Office of Refugee Resettlement
Care Provider Facilities (OMB #: 0970–
0564)
Office of Refugee Resettlement,
Administration for Children and
Families, Department of Health and
Human Services.
ACTION: Request for public comments.
AGENCY:
The Office of Refugee
Resettlement (ORR), Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services, is requesting expedited review
of an information collection request
from the Office of Management and
Budget (OMB). This information
collection will allow the ORR
Unaccompanied Children (UC) Program
to enhance monitoring efforts at care
provider facilities that are not licensed
by the state. A separate notice will be
published inviting public comments on
the proposed collection.
SUPPLEMENTARY INFORMATION:
Description: ACF is requesting
emergency review and approval of this
information collection by OMB, as
authorized under 44 U.S.C. 3507
(subsection j). The proposed forms are
necessary to allow the ORR UC Program
to enhance monitoring efforts at care
provider facilities that are not licensed
by the state. The information collected
is essential to the mission of the agency
and an unanticipated event occurred
that could reasonably result in public
harm if normal Paperwork Reduction
Act (PRA) clearance procedures are
SUMMARY:
followed. A recent proclamation in
Texas (Proclamation by the Governor of
the State of Texas, May 31, 2021) and
recent emergency rule in Florida
(Emergency Rule 65CER21–3, December
10, 2021) has resulted in a large number
of ORR facilities no longer being
licensed by the states. To help mitigate
the issue, ORR plans to perform
quarterly health and safety monitoring
visits to Texas and Florida programs.
The quarterly monitoring visits are in
addition to and do not take the place of
ORR’s existing monitoring activities as
described in UC Policy Guide Section
5.5. In order to implement quarterly
health and safety site visits for
unlicensed programs, ORR is seeking
emergency approval to begin use of
instruments related to this effort as soon
as possible. ORR plans to make minor
edits to 15 existing forms in this
information collection to create the
following alternate versions:
• Unlicensed Facility Site Visit Guide
(Form M–7A–UF)
• Unlicensed Facility Personnel File
Checklist (Form M–10A–UF)
• Unlicensed Facility Program Director
Questionnaire (Form M–11A–UF)
• Unlicensed Facility Clinician
Questionnaire (Form M–11C–UF)
• Unlicensed Facility Case Manager
Questionnaire (Form M–11E–UF)
• Unlicensed Facility Education Staff
Questionnaire (Form M–11G–UF)
• Unlicensed Facility Medical
Coordinator Questionnaire (Form M–
11I–UF)
• Unlicensed Facility Youth Care
Worker Questionnaire (Form M–11J–
UF)
• Unlicensed Facility Prevention of
Sexual Abuse Compliance Manager
Staff Questionnaire (Form M–11K–
UF)
• Unlicensed Facility Interpreter
Questionnaire (Form M–11P–UK)
• Unlicensed Facility UC
Questionnaire—Ages 6–12 Years Old
(Forms M–12A–UF and M–12As–UF)
• Unlicensed Facility UC
Questionnaire—Ages 13 and Older
(Forms M–12B–UF and M–12Bs–UF)
• Unlicensed Facility UC
Questionnaire—Ages 5 and Under
(Form M–12E–UF and M–12Es–UF)
• Unlicensed Facility Legal Service
Provider Questionnaire (Form M–
13C–UF)
• Unlicensed Facility Case Coordinator
Questionnaire (Form M–13E–UF)
Additionally, ORR plans to add the
below form (currently approved under
OMB #0970–0558) to this information
collection as well as the alternate
version listed above to facilitate the
quarterly monitoring on unlicensed
programs.
• Interpreter Questionnaire (Form M–
11P)
Finally, ORR plans to use the
following forms with more than nine
respondents. These were previously
approved by OMB but were removed
from the information collection due to
the number of respondents.
• Unlicensed Facility Monitoring Notes
(Form M–6A–UF)
• Unlicensed Facility UC Case File
Checklist (Form M–7A–UF)
• Unlicensed Facility Onsite
Monitoring Checklist (M–9A–UF)
At this time, ACF is requesting that
OMB grant a 180-day approval for this
request under procedures for expedited
processing. A request for review under
normal procedures will be submitted
within 180 days of the approval for this
request. ACF will invite public
comment through this process. The first
comment period, which invites
comments over a 60-day period, begins
concurrently with the publication of
this notice (see notice titled Proposed
Information Collection Activity;
Monitoring and Compliance for Office of
Refugee Resettlement Care Provider
Facilities (Office of Management and
Budget #: 0970–0564) in this issue of the
Federal Register).
Respondents: ORR grantee and
contractor staff; and UC.
Annual Burden Estimates:
The following burden estimates are
specific to the forms described above
and the subject of this request for
emergency approval. For information
about all currently approved forms
under this OMB number, see: https://
www.reginfo.gov/public/do/
PRAViewICR?ref_nbr=202108-0970-016.
lotter on DSK11XQN23PROD with NOTICES1
ESTIMATED BURDEN HOURS FOR RESPONDENTS
Annual
number of
respondents
Information collection title
Unlicensed Facility Site Visit Guide (Form M–7A–UF) ...................................
Unlicensed Facility UC Case File Checklist (Form M–8A–UF) .......................
Interpreter Questionnaire (Form M–11P) ........................................................
VerDate Sep<11>2014
17:37 Oct 25, 2022
Jkt 259001
PO 00000
Frm 00044
Fmt 4703
Sfmt 4703
Annual
number of
responses per
respondent
56
56
115
E:\FR\FM\26OCN1.SGM
4.0
20.0
2.0
26OCN1
Average
burden hours
per response
1.00
1.00
0.50
Annual total
burden hours
224.00
1,120.00
115.00
]]>Agencies
[Federal Register Volume 87, Number 206 (Wednesday, October 26, 2022)]
[Notices]
[Pages 64795-64797]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-23334]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Agency for Healthcare Research and Quality
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Agency for Healthcare Research and Quality, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: This notice announces the intention of the Agency for
Healthcare Research and Quality (AHRQ) to request that the Office of
Management and Budget (OMB) re-approve the proposed information
collection project ``The Systematic Review Data Repository (SRDR)
Platform''. This proposed information collection was previously
published in the Federal Register on August 12, 2022 and allowed 60
days for public comment. AHRQ did not receive substantive comments
during public review period. The purpose of this notice is to allow an
additional 30 days for public comment.
DATES: Comments on this notice must be received by November 25, 2022.
ADDRESSES: Written 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
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427-1477, or by email at
[email protected].
SUPPLEMENTARY INFORMATION:
Proposed Project
``The Systematic Review Data Repository (SRDR) Platform''
Since 1997, the AHRQ Evidence-based Practice Center (EPC) Program
has been reviewing relevant scientific information on a wide spectrum
of clinical and health services topics to produce various types of
evidence reports. A majority of these evidence reports are systematic
reviews (SRs), which are used as evidence bases for clinical practice
guidelines, research agendas, healthcare coverage, and other health
related policies. Performing SRs is costly in time, labor, and money.
Moreover, there is an increasing expectation of quicker turnaround in
producing SRs to accommodate the fast moving pace of innovations and
new scientific discoveries in healthcare. Some SRs overlap or are
duplicated; independent teams of SR producers often extract data from
the same studies, resulting in replication of work. Current methodology
makes it difficult to harness and reuse previous work when updating
SRs.
In an effort to reduce the economic burden of conducting SRs, the
EPC program undertook development of a collaborative, Web-based
repository of systematic review data called the Systematic Review Data
Repository (SRDR). The OMB Control Number for this data collection is
0935-0244, which was last approved by OMB on October 16, 2019.
This resource serves as both an archive and data extraction tool,
shared among organizations and individuals producing SRs worldwide,
enabling the creation of a central database of SR data. This database
is collaboratively vetted, freely accessible, and integrates seamlessly
with reviewers' existing workflows, with the ultimate goal of
facilitating the efficient generation and update of evidence reviews,
and thus speeding and improving evidence-based policy-making with
regards to health care.
Note that the SRDR system was upgraded during the last period of
OMB clearance and is now designated as SRDR+. We will use the term
``SRDR platform'' to collectively denote the
[[Page 64796]]
various upgraded iterations of the platform.
The SRDR project aims to achieve the following goals:
(1) Create online easy-to-use Web-based tools for conducting
systematic reviews to facilitate extraction of data from primary
studies;
(2) Develop an open-access searchable archive of key questions
addressed in systematic reviews;
(3) Maintain a public repository of primary study data including
provision of technical support for repository users; and
(4) Develop a process for making summary data from systematic
reviews digitally shareable to end-users.
This study is being conducted by AHRQ through its contractor, Brown
University, pursuant to AHRQ's statutory authority to conduct and
support research on healthcare and on systems for the delivery of such
care, including activities with respect to the quality, effectiveness,
efficiency, appropriateness and value of healthcare services, including
database development. 42 U.S.C. 299a(a)(1) and (8).
Method of Collection
To achieve the goals of this project the following data collections
are being implemented:
(1) Collect registration information on SRs from SR producers who
will populate the SRDR platform.
The SRDR platform now uses a two-tiered categorization of users,
and collection of registration data will depend on the type of user.
``Contributors'' are SR producers who use the SRDR platform as a tool
to support production of the SR and share scientific data from their
SRs. Registration data will be collected from these users. ``General
public'' users only view scientific data publicly available in the SRDR
platform. No data will be collected from these users. The
``Commentator'' category of users that were referenced in the last OMB
clearance period has been eliminated in the updated system since no
users have signed up to be commentators. All Contributors undergo a
simple self-registration process by providing a password and an email
address. Provision of username and institution information by
registrants is now optional in the updated system. Collection of
registration data from Contributors is required due to the technical
nature of using the SRDR platform both as a database and a tool for
assisting in the production of a SR, including providing comments in
the various sections of a particular project on the SRDR platform. In
addition, provision of an email address and institution information
allows the administrators of the SRDR platform to confirm that requests
are being made by actual people and not potentially malicious software
code such as bots and other cybersecurity threats.
User registration will be used for administrative purposes only
including communication between SRDR platform administrators and
registrant users. This type of information will not be made publicly
available.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated annualized burden hours for the
respondents' time to participate/use the SRDR platform. In 2020, 1,029
users registered as Contributors. Registration will take approximately
1.5 minutes or 0.025 hours per user. We thus calculate the total burden
hours required for registration for all users annually is 25.73 hours.
Exhibit 1--Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of
Form name Number of responses per Hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Registration of users as Contributors........... 1,029 1 0.025 25.73
---------------------------------------------------------------
Total....................................... 1,029 .............. .............. 25.73
----------------------------------------------------------------------------------------------------------------
Exhibit 2 shows the estimated cost burden associated with the
respondents' time to participate/use the SRDR platform. The total cost
burden to respondents is estimated at an average of $1,126.97 annually.
Exhibit 2--Estimated Annualized Cost Burden
----------------------------------------------------------------------------------------------------------------
Average
Form name Number of Total burden hourly wage Total cost
respondents hours rate * burden
----------------------------------------------------------------------------------------------------------------
Registration of users as Commentators or 1,029 25.73 \a\ $43.80 $1,126.97
Contributors...................................
---------------------------------------------------------------
Total....................................... 1,029 25.73 .............. 1,126.97
----------------------------------------------------------------------------------------------------------------
* National Compensation Survey: Occupational wages in the United States May 2021, ``U.S. Department of Labor,
Bureau of Labor Statistics.'' Available at: https://www.bls.gov/oes/current/oes290000.htm.
\a\ Based on the mean wages for Healthcare Practitioners and Technical Occupations, 29-0000.
Request for Comments
In accordance with the Paperwork Reduction Act, 44 U.S.C. 3501-
3520, comments on AHRQ's information collection are requested with
regard to any of the following: (a) whether the proposed collection of
information is necessary for the proper performance of AHRQ's health
care research and health care information dissemination functions,
including whether the information will have practical utility; (b) the
accuracy of AHRQ's estimate of burden (including hours and costs) of
the proposed collection(s) 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 upon
the respondents, including the use of automated collection techniques
or other forms of information technology.
Comments submitted in response to this notice will be summarized
and included in the Agency's subsequent request for OMB approval of the
[[Page 64797]]
proposed information collection. All comments will become a matter of
public record.
Dated: October 21, 2022.
Marquita Cullom,
Associate Director.
[FR Doc. 2022-23334 Filed 10-25-22; 8:45 am]
BILLING CODE 4160-90-P
