Agency Information Collection Activities: Submission to OMB for Review and Approval; Public Comment Request; The Maternal, Infant, and Early Childhood Home Visiting Program Performance Measurement Information System, OMB No. 0906-0017, Revision, 20372-20374 [2021-07971]
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20372
Federal Register / Vol. 86, No. 73 / Monday, April 19, 2021 / Notices
25. Brett Cassese, Washington, District of
Columbia, Court of Federal Claims No:
21–1055V
26. Rachel Garcia, Boulder, Colorado, Court
of Federal Claims No: 21–1056V
27. Kayla Smith, Cheyenne, Wyoming, Court
of Federal Claims No: 21–1059V
28. Elaine Letizia, Hilton Head, South
Carolina, Court of Federal Claims No:
21–1062V
29. Deborah Gross, Washington, District of
Columbia, Court of Federal Claims No:
21–1063V
30. Marna Brickman, Washington, District of
Columbia, Court of Federal Claims No:
21–1066V
31. Katherine Murphy, Salt Lake City, Utah,
Court of Federal Claims No: 21–1069V
32. Tori Jonet, Luxemburg, Wisconsin, Court
of Federal Claims No: 21–1071V
33. Leah Carter, Washington, District of
Columbia, Court of Federal Claims No:
21–1077V
34. Ethel M. Britt on behalf of Estate of James
E. Britt, Murfreesboro, Tennessee, Court
of Federal Claims No: 21–1078V
35. Adrienne Falzon on behalf of Estate of
Paul Giaccio, Deceased, Atlanta, Georgia,
Court of Federal Claims No: 21–1082V
36. Elizabeth Fordahl, Bismarck, North
Dakota, Court of Federal Claims No: 21–
1086V
37. Hogla Prado, Beaverton, Oregon, Court of
Federal Claims No: 21–1087V
38. Lisa Myers, Winston-Salem, North
Carolina, Court of Federal Claims No:
21–1088V
39. Brandi Rose Wilson, Lenexa, Kansas,
Court of Federal Claims No: 21–1090V
40. Antonio Jackson, Black River Falls,
Wisconsin, Court of Federal Claims No:
21–1091V
41. Sungjin Choi, Prospect Heights, Illinois,
Court of Federal Claims No: 21–1092V
42. Jennifer Counceller, Connersville,
Indiana, Court of Federal Claims No: 21–
1093V
43. Shawntel Denmark, Washington, District
of Columbia, Court of Federal Claims No:
21–1094V
44. Abram Gamino, Washington, District of
Columbia, Court of Federal Claims No:
21–1096V
45. Rachel Page, Washington, District of
Columbia, Court of Federal Claims No:
21–1097V
46. Arianna Reddicks, Phoenix, Arizona,
Court of Federal Claims No: 21–1099V
47. Italo A. Miceli, Rocky Hill, Connecticut,
Court of Federal Claims No: 21–1100V
48. Alice Henningsen, Wichita, Kansas, Court
of Federal Claims No: 21–1101V
49. Randall Schutz, Chicago, Illinois, Court of
Federal Claims No: 21–1103V
50. Camille Dumentat, Severna Park,
Maryland, Court of Federal Claims No:
21–1104V
51. Melanie Muhlstock and Todd Muhlstock
on behalf of A.M., Phoenix, Arizona,
Court of Federal Claims No: 21–1106V
52. Stephen Ziegler, Lincoln, Nebraska, Court
of Federal Claims No: 21–1109V
53. Bernetta Polley, Mankato, Minnesota,
Court of Federal Claims No: 21–1111V
54. Carol Lloyd, Sicklerville, New Jersey,
Court of Federal Claims No: 21–1112V
VerDate Sep<11>2014
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55. Andrea Jordan, Hillsboro, Oregon, Court
of Federal Claims No: 21–1113V
56. Greta Sessoms, Virginia Beach, Virginia,
Court of Federal Claims No: 21–1120V
57. Ruth Williams, Washington, District of
Columbia, Court of Federal Claims No:
21–1121V
58. Paulette Penzvalto, Washington, District
of Columbia, Court of Federal Claims No:
21–1122V
59. Rebecca Hawes, Nitro, West Virginia,
Court of Federal Claims No: 21–1124V
60. Jennifer Puckett, Montgomery, Alabama,
Court of Federal Claims No: 21–1125V
61. Sheryl Young, Washington, District of
Columbia, Court of Federal Claims No:
21–1126V
62. Harold Sykes, Washington, District of
Columbia, Court of Federal Claims No:
21–1127V
63. Sharon Dunn, Washington, District of
Columbia, Court of Federal Claims No:
21–1128V
64. Matthew Caruso on behalf of L.C.,
Hollidaysburg, Pennsylvania, Court of
Federal Claims No: 21–1131V
65. Donald Holmberg, Erie, Pennsylvania,
Court of Federal Claims No: 21–1132V
66. Roman Gelevan, Bronx, New York, Court
of Federal Claims No: 21–1133V
67. Jimmy Zavala, Boscobel, Wisconsin,
Court of Federal Claims No: 21–1134V
68. Taylor Wickline, Phoenix, Arizona, Court
of Federal Claims No: 21–1135V
69. Michael Wakileh, Costa Mesa, California,
Court of Federal Claims No: 21–1136V
70. Barbara McNair, New Lenox, Illinois,
Court of Federal Claims No: 21–1139V
71. Kerrie Burkett, Phoenix, Arizona, Court of
Federal Claims No: 21–1140V
72. Ngoc H. Lam, Greenville, South Carolina,
Court of Federal Claims No: 21–1141V
73. Donald Olson, Seattle, Washington, Court
of Federal Claims No: 21–1142V
74. Ashton Schultz, Englewood, New Jersey,
Court of Federal Claims No: 21–1144V
75. Kotana Cromartie, Washington, District of
Columbia, Court of Federal Claims No:
21–1145V
76. Jennifer Soileau, Englewood, New Jersey,
Court of Federal Claims No: 21–1146V
[FR Doc. 2021–07970 Filed 4–16–21; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Submission to OMB for
Review and Approval; Public Comment
Request; The Maternal, Infant, and
Early Childhood Home Visiting
Program Performance Measurement
Information System, OMB No. 0906–
0017, Revision
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
PO 00000
Frm 00012
Fmt 4703
Sfmt 4703
In compliance with of the
Paperwork Reduction Act of 1995,
HRSA has submitted an Information
Collection Request (ICR) to the Office of
Management and Budget (OMB) for
review and approval. Comments
submitted during the first public review
of this ICR will be provided to OMB.
OMB will accept further comments from
the public during the review and
approval period. OMB may act on
HRSA’s ICR only after the 30 day
comment period for this notice has
closed.
DATES: Comments on this ICR should be
received no later than May 19, 2021.
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 Review—Open for
Public Comments’’ or by using the
search function.
FOR FURTHER INFORMATION CONTACT: To
request a copy of the clearance requests
submitted to OMB for review, email Lisa
Wright-Solomon, the HRSA Information
Collection Clearance Officer at
paperwork@hrsa.gov or call (301) 443–
1984.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title:
The Maternal, Infant, and Early
Childhood Home Visiting Program
Performance Measurement Information
System, OMB NO. 0906–0017, Revision.
Abstract: This clearance request is for
continued approval of the Maternal,
Infant, and Early Childhood Home
Visiting (MIECHV) Program
Performance Measurement Information
System, as updated. The MIECHV
Program, administered by HRSA in
partnership with the Administration for
Children and Families, supports
voluntary, evidence-based home visiting
services to pregnant women and to
parents with young children up to
kindergarten entry. States, certain nonprofit organizations, and tribal entities
are eligible to receive funding from the
MIECHV Program and have the
flexibility to tailor the program to serve
the specific needs of their communities.
A 60-day notice published in the
Federal Register on December 18, 2020,
vol. 85, No. 244; pp. 82490–91. There
were 24 public comments.
These comments provided
suggestions to improve clarity, protect
privacy, and reduce reporting burden
related to information complexity in
Form 1. Comments also suggested ways
to enhance the quality, utility, and
clarity of existing guidance in Form 2
SUMMARY:
E:\FR\FM\19APN1.SGM
19APN1
20373
Federal Register / Vol. 86, No. 73 / Monday, April 19, 2021 / Notices
and suggested that the implementation
of two newly proposed measures related
to substance use screening and referrals
would require updates to training
activities and data collection.
HRSA appreciates these comments
and recommended revisions to the
information collection. HRSA has
responded to the recommended
revisions by revising certain
demographic categories, removing a
proposed table on father and caregiver
engagement, making the reporting of
proposed measures on substance use
screening and referrals optional, and
increasing the estimated burden on
respondents due to the inclusion of two
new optional measures (Form 2) for
substance use and referral that are being
introduced through this revision. HRSA
intends for the following proposed
revisions to the data collection for the
MIECHV Program to further improve
clarity, protect privacy, and address
increased reporting burden:
• Form 1, Table 1: Update table to
include reporting for gender non-binary
participants and unknown/did not
report participant gender.
• Form 1, Tables 3, 5, 6, 7, 18, 19, and
20: Update tables to remove index child
gender reporting.
• Form 1, Tables 3, 4, 6, 7, 8, 9, 10,
11, and 18: Update tables to remove
adult participant gender reporting.
• Form 1, Table 15: Change table title
to ‘‘Home Visits.’’
• Form 1, Table 15: Update table to
collect the number of home visits
completed virtually.
• Form 1, Tables 4, 9, 10, and 18:
Update tables to include reporting for
new and continuing adult participants.
• Form 1, Tables 5, 19, and 20:
Update tables to include reporting for
new and continuing index children.
• Form 2, Measure 13: Change
measure name to ‘‘Behavioral Concern
Inquiries.’’
• Form 2, Measure 16: Update
measure to reflect caregiver health
insurance coverage status.
• Form 2, Measures 17, 18, and 19:
Update missing data guidance.
• Form 2: Inclusion of two optional
measures to collect information on
subtance use screening and referrals.
Need and Proposed Use of the
Information: HRSA uses performance
information to demonstrate program
accountability and continuously
monitor and provide oversight to
MIECHV Program awardees. The
information is also used to provide
quality improvement guidance and
technical assistance to awardees and
help inform the development of early
childhood systems at the national, state,
and local level. HRSA is seeking to
revise and extend demographic, service
utilization, and select clinical indicators
for participants enrolled in home
visiting services. In addition, HRSA will
collect a set of standardized
performance and outcome indicators
that correspond with the statutorily
identified benchmark areas.
This information will be used to
demonstrate awardees’ compliance with
legislative and programmatic
requirements. It will also be used to
monitor and provide continued
oversight for awardee performance and
to target technical assistance resources
to awardees. In the future, HRSA
anticipates that MIECHV funding
decisions may be allocated, in part,
based on awardee performance,
including on benchmark performance
areas. This notice is subject to the
appropriation of funds, and is a
contingency action taken to ensure that,
should funds become available for this
purpose, information can be collected in
a timely manner.
Likely Respondents: MIECHV Program
awardees that are states, territories, and,
where applicable, nonprofit
organizations providing home visiting
services within states.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Form 1: Demographic, Service Utilization, and Select Clinical Indicators ...................................................................
Form 2: Performance Indicators and Systems Outcome
Measures ..........................................................................
jbell on DSKJLSW7X2PROD with NOTICES
Total ..............................................................................
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17:11 Apr 16, 2021
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PO 00000
Frm 00013
Fmt 4703
Number of
responses
per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
56
1
56
440
24,640
56
1
56
360
20,160
56
........................
56
........................
44,800
Sfmt 9990
E:\FR\FM\19APN1.SGM
19APN1
20374
Federal Register / Vol. 86, No. 73 / Monday, April 19, 2021 / Notices
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions, (2) the accuracy of the
estimated burden, (3) ways to enhance
the quality, utility, and clarity of the
information to be collected, and (4) the
use of automated collection techniques
or other forms of information
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021–07971 Filed 4–16–21; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: National
Survey of Organ Donation Attitudes
and Practices, OMB No. 0915–0290—
Extension
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
AGENCY:
ACTION:
Notice.
In compliance with the
Paperwork Reduction Act of 1995,
HRSA announces plans to submit an
Information Collection Request (ICR),
described below, to the Office of
Management and Budget (OMB). Prior
to submitting the ICR to OMB, HRSA
seeks comments from the public
SUMMARY:
regarding the burden estimate below or
any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than June 18, 2021.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or mail the HRSA
Information Collection Clearance
Officer, 14N136B, 5600 Fishers Lane,
Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Lisa Wright-Solomon, the HRSA
Information Collection Clearance Officer
at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information request collection title for
reference.
Information Collection Request Title:
National Survey of Organ Donation
Attitudes and Practices, OMB No. 0915–
0290—Extension.
Abstract: HRSA is requesting
approval by OMB for a revision of a
previously approved collection of
information (OMB control number
0915–0290). The National Survey of
Organ Donation Attitudes and Practices
(NSODAP) is conducted approximately
every 6–7 years and serves a critical role
in providing HRSA and the donation
community with data regarding why
Americans choose to donate organs,
current barriers to donation, and
possible paths to increasing donations.
Survey data and derived analytic
insights help HRSA develop and target
appropriate messages for public
outreach and educational initiatives.
Need and Proposed Use of the
Information: HRSA is the primary
federal entity responsible for oversight
of the solid organ and blood stem cell
transplant systems and initiatives to
increase organ donor registration and
donation in the United States. This
survey is the primary method by which
HRSA can obtain information from
Americans about organ donation
attitudes and beliefs. OMB previously
approved this survey and HRSA fielded
it during 2005, 2012, and 2019. Results
of the data collected from this survey
will help develop appropriate messages
for future public outreach and
educational initiatives to increase
awareness about organ donation and
ultimately the number of registered
donors.
Likely Respondents: A nationally
representative sample of adults over the
age of 18 with a higher number of
responses from populations of interest
such as racial-ethnic minorities,
including African American, Asian,
Native American, and Hispanic
respondents, as well as respondents of
all age groups and education levels.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install, and utilize
technology and systems for collecting,
validating, verifying, processing and
maintaining information, and disclosing
and providing information; to train
personnel and be able to respond to a
collection of information; to search data
sources; to complete and review the
collection of information, and to
transmit or otherwise disclose the
information. A summary of the total
annual burden hours estimated for this
ICR is in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
jbell on DSKJLSW7X2PROD with NOTICES
Number of
responses per
respondent
Number of
respondents
Form name
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
NSODAP Revised Survey—Telephone .............................
NSODAP Revised Survey—Online Panel .........................
2,000
8,000
1
1
2,000
8,000
0.37
0.27
740
2,160
Total ............................................................................
10,000
..........................
10,000
........................
2,900
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
VerDate Sep<11>2014
17:11 Apr 16, 2021
Jkt 253001
or other forms of information
technology to minimize the information
collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021–07996 Filed 4–16–21; 8:45 am]
BILLING CODE 4165–15–P
PO 00000
Frm 00014
Fmt 4703
Sfmt 4703
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the COVID–19 Health Equity
Task Force
Office of the Assistant
Secretary for Health, Office of the
Secretary, Department of Health and
Human Services.
AGENCY:
E:\FR\FM\19APN1.SGM
19APN1
]]>Agencies
[Federal Register Volume 86, Number 73 (Monday, April 19, 2021)]
[Notices]
[Pages 20372-20374]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07971]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Submission to OMB for
Review and Approval; Public Comment Request; The Maternal, Infant, and
Early Childhood Home Visiting Program Performance Measurement
Information System, OMB No. 0906-0017, Revision
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with of the Paperwork Reduction Act of 1995,
HRSA has submitted an Information Collection Request (ICR) to the
Office of Management and Budget (OMB) for review and approval. Comments
submitted during the first public review of this ICR will be provided
to OMB. OMB will accept further comments from the public during the
review and approval period. OMB may act on HRSA's ICR only after the 30
day comment period for this notice has closed.
DATES: Comments on this ICR should be received no later than May 19,
2021.
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 Review--Open for
Public Comments'' or by using the search function.
FOR FURTHER INFORMATION CONTACT: To request a copy of the clearance
requests submitted to OMB for review, email Lisa Wright-Solomon, the
HRSA Information Collection Clearance Officer at [email protected] or
call (301) 443-1984.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title: The Maternal, Infant, and
Early Childhood Home Visiting Program Performance Measurement
Information System, OMB NO. 0906-0017, Revision.
Abstract: This clearance request is for continued approval of the
Maternal, Infant, and Early Childhood Home Visiting (MIECHV) Program
Performance Measurement Information System, as updated. The MIECHV
Program, administered by HRSA in partnership with the Administration
for Children and Families, supports voluntary, evidence-based home
visiting services to pregnant women and to parents with young children
up to kindergarten entry. States, certain non-profit organizations, and
tribal entities are eligible to receive funding from the MIECHV Program
and have the flexibility to tailor the program to serve the specific
needs of their communities.
A 60-day notice published in the Federal Register on December 18,
2020, vol. 85, No. 244; pp. 82490-91. There were 24 public comments.
These comments provided suggestions to improve clarity, protect
privacy, and reduce reporting burden related to information complexity
in Form 1. Comments also suggested ways to enhance the quality,
utility, and clarity of existing guidance in Form 2
[[Page 20373]]
and suggested that the implementation of two newly proposed measures
related to substance use screening and referrals would require updates
to training activities and data collection.
HRSA appreciates these comments and recommended revisions to the
information collection. HRSA has responded to the recommended revisions
by revising certain demographic categories, removing a proposed table
on father and caregiver engagement, making the reporting of proposed
measures on substance use screening and referrals optional, and
increasing the estimated burden on respondents due to the inclusion of
two new optional measures (Form 2) for substance use and referral that
are being introduced through this revision. HRSA intends for the
following proposed revisions to the data collection for the MIECHV
Program to further improve clarity, protect privacy, and address
increased reporting burden:
Form 1, Table 1: Update table to include reporting for
gender non-binary participants and unknown/did not report participant
gender.
Form 1, Tables 3, 5, 6, 7, 18, 19, and 20: Update tables
to remove index child gender reporting.
Form 1, Tables 3, 4, 6, 7, 8, 9, 10, 11, and 18: Update
tables to remove adult participant gender reporting.
Form 1, Table 15: Change table title to ``Home Visits.''
Form 1, Table 15: Update table to collect the number of
home visits completed virtually.
Form 1, Tables 4, 9, 10, and 18: Update tables to include
reporting for new and continuing adult participants.
Form 1, Tables 5, 19, and 20: Update tables to include
reporting for new and continuing index children.
Form 2, Measure 13: Change measure name to ``Behavioral
Concern Inquiries.''
Form 2, Measure 16: Update measure to reflect caregiver
health insurance coverage status.
Form 2, Measures 17, 18, and 19: Update missing data
guidance.
Form 2: Inclusion of two optional measures to collect
information on subtance use screening and referrals.
Need and Proposed Use of the Information: HRSA uses performance
information to demonstrate program accountability and continuously
monitor and provide oversight to MIECHV Program awardees. The
information is also used to provide quality improvement guidance and
technical assistance to awardees and help inform the development of
early childhood systems at the national, state, and local level. HRSA
is seeking to revise and extend demographic, service utilization, and
select clinical indicators for participants enrolled in home visiting
services. In addition, HRSA will collect a set of standardized
performance and outcome indicators that correspond with the statutorily
identified benchmark areas.
This information will be used to demonstrate awardees' compliance
with legislative and programmatic requirements. It will also be used to
monitor and provide continued oversight for awardee performance and to
target technical assistance resources to awardees. In the future, HRSA
anticipates that MIECHV funding decisions may be allocated, in part,
based on awardee performance, including on benchmark performance areas.
This notice is subject to the appropriation of funds, and is a
contingency action taken to ensure that, should funds become available
for this purpose, information can be collected in a timely manner.
Likely Respondents: MIECHV Program awardees that are states,
territories, and, where applicable, nonprofit organizations providing
home visiting services within states.
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose, or provide the
information requested. This includes the time needed to review
instructions; to develop, acquire, install, and utilize technology and
systems for the purpose of collecting, validating, and verifying
information, processing and maintaining information, and disclosing and
providing information; to train personnel and to be able to respond to
a collection of information; to search data sources; to complete and
review the collection of information; and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of Total burden per Total burden
Form name respondents responses per responses response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Form 1: Demographic, Service 56 1 56 440 24,640
Utilization, and Select
Clinical Indicators............
Form 2: Performance Indicators 56 1 56 360 20,160
and Systems Outcome Measures...
-------------------------------------------------------------------------------
Total....................... 56 .............. 56 .............. 44,800
----------------------------------------------------------------------------------------------------------------
[[Page 20374]]
HRSA specifically requests comments on (1) the necessity and
utility of the proposed information collection for the proper
performance of the agency's functions, (2) the accuracy of the
estimated burden, (3) ways to enhance the quality, utility, and clarity
of the information to be collected, and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021-07971 Filed 4-16-21; 8:45 am]
BILLING CODE P
