Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; State Performance Report [OMB #0985-New], 27625-27626 [2021-10708]
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27625
Federal Register / Vol. 86, No. 97 / Friday, May 21, 2021 / Notices
Comments due within 30 days of
publication. OMB must make a decision
about the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
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.
DATES:
Description: The COVID–19 pandemic
has had profound effects on the U.S.
economy, on the healthcare sector and
on individuals and families across the
country. The pandemic has also had
broad implications for HPOG 2.0
programs—on how and how much
healthcare training is delivered, on
demand for healthcare workers, on
interest in working in health care, and
on the labor market more broadly. OPRE
seeks to understand the particular
experiences of those who apply for the
HPOG Program during this period by
surveying study participants enrolled
after the onset of the pandemic. The
COVID Cohort Survey would collect
important information on participant
experiences 15 months after
randomization and would allow the
impact study to compare impacts for
pre-COVID participants with impacts for
those enrolled after the onset the
pandemic.
Respondents: HPOG impact study
participants from the 27 non-tribal
HPOG 2.0 grantees (treatment and
control group members who enroll
between May 2020 and September
2021).
Annual Burden Estimates: This
request is specific to the COVID Cohort
Survey. Currently approved materials
and associated burden can be found at:
https://www.reginfo.gov/public/do/
PRAICList?ref_nbr=201904-0970-006.
Instrument
Number of
respondents
(total over
request
period)
Number of
responses per
respondent
(total over
request
period)
Average
burden per
response
(in hours)
Total burden
(in hours)
Annual burden
(in hours)
Instrument 12a: COVID–19 Cohort Survey .........................
5,625
1
1
5,625
1,875
Estimated Total Annual Burden
Hours: 1,875.
Authority: Section 2008 of the Social
Security Act as enacted by Section 5507 of
the Affordable Care Act and Section 413 of
the Social Security Act, 42 U.S.C. 613.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–10732 Filed 5–20–21; 8:45 am]
BILLING CODE 4184–72–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request;
State Performance Report [OMB
#0985–New]
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
The Administration for
Community Living is announcing that
the proposed collection of information
listed above has been submitted to the
Office of Management and Budget
(OMB) for review and clearance as
required under section 506(c)(2)(A) of
the Paperwork Reduction Act of 1995.
This 30-Day notice collects comments
on the information collection
requirements related to the State
Performance Report. This notice solicits
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
SUPPLEMENTARY INFORMATION:
VerDate Sep<11>2014
17:15 May 20, 2021
Jkt 253001
comments on the new information
collection requirements relating to the
State Performance Report.
DATES: Comments on the collection of
information must be submitted
electronically by 11:59 p.m. (EST) or
postmarked by June 21, 2021.
ADDRESSES: Submit written comments
and recommendations for the proposed
information collection within 30 days of
publication of this notice to
www.reginfo.gov/public/do/PRAMain.
Find the information collection by
selecting ‘‘Currently under 30-day
Review—Open for Public Comments’’ or
by using the search function. By mail to
the Office of Information and Regulatory
Affairs, OMB, New Executive Office
Bldg., 725 17th St. NW, Rm. 10235,
Washington, DC 20503, Attn: OMB Desk
Officer for ACL.
FOR FURTHER INFORMATION CONTACT:
Susan Jenkins, Administration for
Community Living, Washington, DC
20201, by email at Susan.Jenkins@
acl.hhs.gov or by telephone at 202–795–
7369.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, ACL
has submitted the following proposed
collection of information to OMB for
review and clearance.
The Administration for Community
Living (ACL) is requesting approval to
collect data for the currently approved
SPR under 0985–0008 expiring in FY
2022, which is the final reporting year
for the currently approved OMB control
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number (0985–0008). In order to comply
with requirements under the PRA it is
necessary to place this ‘‘new SPR’’ IC
under a new OMB control number while
keeping the currently approved SPR
under 0985–0008 active for remaining
reporting in FY 2022.
The purpose of this data collection is
to fulfill requirements of the Older
Americans Act and the Government
Performance and Results Modernization
Act (GPRA Modernization Act) of 2010
and related program performance
activities.
Section 202(a)(16) of the OAA
requires the collection of statistical data
regarding the programs and activities
carried out with funds provided under
the OAA and Section 207(a) directs the
Assistant Secretary on Aging to prepare
and submit a report to the President and
Congress based on those data.
Section 202(f) directs the Assistant
Secretary to develop a set of
performance outcome measures for
planning, managing, and evaluating
activities performed and services
provided under the OAA. Requirements
pertaining to the measurement and
evaluation of the impact of all programs
authorized by the OAA described in
section 206(a). The State Performance
Report is one source of data used to
develop and report performance
outcome measures and measure
program effectiveness in achieving the
stated goals of the OAA.
The Administration on Aging (now
within the Administration for
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21MYN1
27626
Federal Register / Vol. 86, No. 97 / Friday, May 21, 2021 / Notices
Community Living) first developed a
State Program Report (SPR) in 1996 as
part of its National Aging Program
Information System (NAPIS). The SPR
collects information about the national
Aging Network, how State Agencies on
Aging expend their OAA funds as well
as funding from other sources for OAA
authorized supportive services. The SPR
also collects information on the
demographic and functional status of
the recipients, and is a key source for
ACL performance measurement. This
previously approved ‘‘New SPR’’ was a
revision of the currently active version
(effective 2019–2022) and approved in
2018, also assigned with the same OMB
Control Number #0985–0001. This
previously approved collection reduces
the number of data elements reported by
70% compared to the 2019–2022 SPR.
ACL intends to seek a new OMB
Control Number for the for the new SPR
effective FY 2022–2025.
This request applies only to making
an administrative change to the 2018
approved version of the State
Performance Report for State Units on
Aging (Older Americans Act Titles III
Number of
respondents
Respondent/data collection activity
Responses
per
respondent
Hours per
response
Annual
burden hours
SPR ..................................................................................................................
56
1
33.5
1,876
Total ..........................................................................................................
56
1
33.5
1,876
Dated: May 17, 2021.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2021–10708 Filed 5–20–21; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2021–N–0441]
Cardiovascular and Renal Drugs
Advisory Committee; Notice of
Meeting; Establishment of a Public
Docket; Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice; establishment of a
public docket; request for comments.
ACTION:
The Food and Drug
Administration (FDA) announces a
forthcoming public advisory committee
meeting of the Cardiovascular and Renal
Drugs Advisory Committee. The general
function of the committee is to provide
advice and recommendations to FDA on
regulatory issues. The meeting will be
open to the public. FDA is establishing
a docket for public comment on this
document.
SUMMARY:
The meeting will be held
virtually on July 15, 2021, from 10 a.m.
to 5 p.m. Eastern Time.
ADDRESSES: Please note that due to the
impact of the COVID–19 pandemic, all
meeting participants will be joining this
advisory committee meeting via an
online teleconferencing platform.
Answers to commonly asked questions
DATES:
jbell on DSKJLSW7X2PROD with NOTICES
and VII (Chapters 3 and 4) (‘‘new SPR’’).
ACL intends to use this proposed data
to collect information with the FY 2022
reporting year.
Comments in Response to the 60-Day
Federal Register Notice: ACL published
a 60-day notice in the Federal Register
soliciting public comments on February
25, 2021, Volume 86, Number 36, pages
11541–11542. ACL received no
comments.
Estimated Program Burden: ACL
estimates an annual burden of 1,876
hours.
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about FDA advisory committee meetings
may be accessed at: https://
www.fda.gov/AdvisoryCommittees/
AboutAdvisoryCommittees/
ucm408555.htm.
FDA is establishing a docket for
public comment on this meeting. The
docket number is FDA–2021–N–0441.
The docket will close on July 14, 2021.
Submit either electronic or written
comments on this public meeting by
July 14, 2021. Please note that late,
untimely filed comments will not be
considered. Electronic comments must
be submitted on or before July 14, 2021.
The https://www.regulations.gov
electronic filing system will accept
comments until 11:59 p.m. Eastern Time
at the end of July 14, 2021. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
acceptance receipt is on or before that
date.
Comments received on or before June
30, 2021, will be provided to the
committee. Comments received after
that date will be taken into
consideration by FDA. In the event that
the meeting is cancelled, FDA will
continue to evaluate any relevant
applications or information, and
consider any comments submitted to the
docket, as appropriate.
You may submit comments as
follows:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
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including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2021–N–0441 for ‘‘Cardiovascular and
Renal Drugs Advisory Committee;
Notice of Meeting; Establishment of a
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]]>Agencies
[Federal Register Volume 86, Number 97 (Friday, May 21, 2021)]
[Notices]
[Pages 27625-27626]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-10708]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Submission for OMB
Review; Public Comment Request; State Performance Report [OMB #0985-
New]
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living is announcing that the
proposed collection of information listed above has been submitted to
the Office of Management and Budget (OMB) for review and clearance as
required under section 506(c)(2)(A) of the Paperwork Reduction Act of
1995. This 30-Day notice collects comments on the information
collection requirements related to the State Performance Report. This
notice solicits comments on the new information collection requirements
relating to the State Performance Report.
DATES: Comments on the collection of information must be submitted
electronically by 11:59 p.m. (EST) or postmarked by June 21, 2021.
ADDRESSES: Submit written comments and recommendations for the proposed
information collection within 30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain. Find the information collection by
selecting ``Currently under 30-day Review--Open for Public Comments''
or by using the search function. By mail to the Office of Information
and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St.
NW, Rm. 10235, Washington, DC 20503, Attn: OMB Desk Officer for ACL.
FOR FURTHER INFORMATION CONTACT: Susan Jenkins, Administration for
Community Living, Washington, DC 20201, by email at
[email protected] or by telephone at 202-795-7369.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, ACL has
submitted the following proposed collection of information to OMB for
review and clearance.
The Administration for Community Living (ACL) is requesting
approval to collect data for the currently approved SPR under 0985-0008
expiring in FY 2022, which is the final reporting year for the
currently approved OMB control number (0985-0008). In order to comply
with requirements under the PRA it is necessary to place this ``new
SPR'' IC under a new OMB control number while keeping the currently
approved SPR under 0985-0008 active for remaining reporting in FY 2022.
The purpose of this data collection is to fulfill requirements of
the Older Americans Act and the Government Performance and Results
Modernization Act (GPRA Modernization Act) of 2010 and related program
performance activities.
Section 202(a)(16) of the OAA requires the collection of
statistical data regarding the programs and activities carried out with
funds provided under the OAA and Section 207(a) directs the Assistant
Secretary on Aging to prepare and submit a report to the President and
Congress based on those data.
Section 202(f) directs the Assistant Secretary to develop a set of
performance outcome measures for planning, managing, and evaluating
activities performed and services provided under the OAA. Requirements
pertaining to the measurement and evaluation of the impact of all
programs authorized by the OAA described in section 206(a). The State
Performance Report is one source of data used to develop and report
performance outcome measures and measure program effectiveness in
achieving the stated goals of the OAA.
The Administration on Aging (now within the Administration for
[[Page 27626]]
Community Living) first developed a State Program Report (SPR) in 1996
as part of its National Aging Program Information System (NAPIS). The
SPR collects information about the national Aging Network, how State
Agencies on Aging expend their OAA funds as well as funding from other
sources for OAA authorized supportive services. The SPR also collects
information on the demographic and functional status of the recipients,
and is a key source for ACL performance measurement. This previously
approved ``New SPR'' was a revision of the currently active version
(effective 2019-2022) and approved in 2018, also assigned with the same
OMB Control Number #0985-0001. This previously approved collection
reduces the number of data elements reported by 70% compared to the
2019-2022 SPR.
ACL intends to seek a new OMB Control Number for the for the new
SPR effective FY 2022-2025.
This request applies only to making an administrative change to the
2018 approved version of the State Performance Report for State Units
on Aging (Older Americans Act Titles III and VII (Chapters 3 and 4)
(``new SPR''). ACL intends to use this proposed data to collect
information with the FY 2022 reporting year.
Comments in Response to the 60-Day Federal Register Notice: ACL
published a 60-day notice in the Federal Register soliciting public
comments on February 25, 2021, Volume 86, Number 36, pages 11541-11542.
ACL received no comments.
Estimated Program Burden: ACL estimates an annual burden of 1,876
hours.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Annual burden
Respondent/data collection activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
SPR............................................. 56 1 33.5 1,876
---------------------------------------------------------------
Total....................................... 56 1 33.5 1,876
----------------------------------------------------------------------------------------------------------------
Dated: May 17, 2021.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2021-10708 Filed 5-20-21; 8:45 am]
BILLING CODE 4154-01-P
