Agency Information Collection Activities: Proposed Collection; Public Comment Request of the State Councils on Developmental Disabilities (Councils) OMB Control Number 0985-0033, 58356-58357 [2022-20796]
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Federal Register / Vol. 87, No. 185 / Monday, September 26, 2022 / Notices
2. SUPPLEMENTAL CENTERS FOR DISEASE CONTROL (CDC)—Continued
# Hours dedicated to task
Hourly rate of task
Totals
Current annual effort
Mean
Range
Mean
Range
Average effort
per center
Across the
network
(average effort
× 67 centers)
Data entry & cleaning Computer User
Support Specialist ................................
15
380–820
27.72
$16–43
415.8
$27,858.6
Subtotal .............................................
Fringe Rate 100% ....................................
76
........................
728–2,706
........................
$162.10
........................
........................
........................
$3,310.16
$3,310.16
221,778.72
221,778.72
Total Current Burden ........................
76
........................
........................
........................
........................
........................
3. SUPPLEMENTAL PUBLIC HEALTH WORKFORCE
# Hours dedicated to task
Hourly rate of task
Totals
Current annual effort
Mean
Design of data tools Computer Systems
Analyst ................................................
Staff train-data collection Training & Development Manager ............................
Data gathering & verifying Computer
User Support Specialist ......................
Data entry & cleaning Computer User
Support Specialist ..............................
Range
Mean
Average effort
per center
Range
Across the
network
(average effort
× 67 centers)
4
1–50
$49.10
$24–75
196.4
13,158.80
6
20–40
$57.56
$29–71
345.36
23,139.12
4
200–2,184
$27.72
$16–43
110.88
$7,428.96
4
380–820
27.72
$16–43
110.88
$7,428.96
Subtotal ...........................................
Fringe Rate 100% ..................................
18
........................
728–2,706
........................
162.10
........................
........................
........................
$763.52
$763.52
$51,155.84
$51,155.84
Total Current Burden ......................
18
........................
........................
........................
........................
..........................
The above figures related to the
percentage of hours dedicated to
different tasks were developed from
information gathered by the UCEDD
technical assistance provider for the
previous data information collection
request.
Date: September 20, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2022–20797 Filed 9–23–22; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities: Proposed Collection; Public
Comment Request of the State
Councils on Developmental Disabilities
(Councils) OMB Control Number 0985–
0033
Administration for Community
Living, Department of Health and
Human Services.
ACTION: Notice.
AGENCY:
VerDate Sep<11>2014
16:43 Sep 23, 2022
Jkt 256001
The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
comment on the proposed collection of
information listed above. Under the
Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to
publish a notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This Information Collection (IC)
Revision solicits comments on the
information collection requirements
relating to the State Councils on
Developmental Disabilities (Councils)
OMB control number 0985–0033.
SUMMARY:
Comments on the collection of
information must be submitted
electronically by 11:59 p.m. (EST) or
postmarked by November 25, 2022.
DATES:
Submit electronic
comments on the collection of
information to Sara Newell-Perez at
Sara.Newell-Perez@acl.hhs.gov. Submit
electronic comments on the collection
of information to Administration for
Community Living, 330 C Street SW,
ADDRESSES:
PO 00000
Frm 00049
Fmt 4703
Sfmt 4703
Washington, DC 20201, Attention: Sara
Newell-Perez.
FOR FURTHER INFORMATION CONTACT: Sara
Newell-Perez, 202–795–7413 or
Sara.Newell-Perez@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
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.
‘‘Collection of information’’ is defined
in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
The PRA requires Federal agencies to
provide a 60-day notice in the Federal
Register concerning each proposed
collection of information, including
each proposed extension of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, ACL is publishing a notice
of the proposed collection of
information set forth in this document.
With respect to the collection of
information described below, ACL
invites comments on our burden
E:\FR\FM\26SEN1.SGM
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58357
Federal Register / Vol. 87, No. 185 / Monday, September 26, 2022 / Notices
estimates or any other aspect of this
collection of information, including:
(1) whether the proposed collection of
information is necessary for the proper
performance of ACL’s functions,
including whether the information will
have practical utility;
(2) the accuracy of ACL’s estimate of
the burden of the proposed collection of
information, including the validity of
the methodology and assumptions used
to determine burden estimates;
(3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) ways to minimize the burden of
the collection of information on
respondents, including through the use
of automated collection techniques
when appropriate, and other forms of
information technology.
The State Councils on Developmental
Disabilities (Councils) are authorized by
Subtitle B of the Developmental
Disabilities Assistance and Bill of Rights
Act of 2000 (DD Act), as amended, [42
U.S.C. 15001 et seq.] (The DD Act). The
DD Act requires Councils to submit an
annual Program Performance Report.
Section 125(c)(7) (42 U.S.C. 15025),
states that: Beginning in fiscal year
2002, the Council shall annually
prepare and transmit to the Secretary a
report. Each report shall be in a form
prescribed by the Secretary by
regulation under section 104(b). Each
report shall contain information about
the progress made by the Council in
achieving the goals of the Council as
specified in section 124(c)(4)).
The Council is responsible for the
development and submission of the
PPR, and for reporting on performance
measure data related to its progress in
carrying out the goals and objectives of
the State Plan. The data collected in the
PPR and submitted to ACL is also used
to comply with the GPRA
Modernization Act of 2010 (GPRAMA).
Performance measure results are
reported to Congress under GPRAMA.
This is a revision of a currently
approved information collection that
expires in 2023. To ensure the DD
Council PPR is consistent with the
Executive Order on Advancing Racial
Equity and Support for Underserved
Communities Through the Federal
Government and the Executive Order on
Advancing Equality for Lesbian, Gay,
Bisexual, Transgender, Queer, and
Intersex Individuals, ACL intends to
determine whether the sexual
orientation and gender identity (SOGI)
data elements need to be adapted prior
to adding them to ensure accessibility of
the questions for individuals with
intellectual and developmental
disabilities.
This IC will also include elements
needed to account for the activities
supported by funding from the Centers
for Disease Control and Prevention
(CDC) to support access to vaccines for
people with disabilities as well as the
funds awarded under the American
Rescue Plan to increase the Public
Health Workforce (PHWF). All other
elements of the template remain
consistent with previously approved
Number of
respondents
Respondent/data collection activity
performance measures and corresponds
to requirements in the DD Act.
The information collected from the
DD Councils is used for multiple
purposes:
(1) To develop and submit at least
every two years a report to the
President, Congress, and the National
Council on Disability that describes the
goals and outcomes of programs
supported under the DD Act.
(2) As a tool for DD Councils to
measure and report on progress in
reaching goals and identify areas for
which revisions are indicated;
(3) To enhance the Federal project
officers’ monitoring of DD Council
progress in reaching projected
outcomes;
(4) As a set of performance measures
that will yield a national portrait of DD
Council program impact; and
(5) For Congress and the
Administration in making funding and
appropriation decisions with regard to
the DD Council program.
The proposed data collection tools
may be found on the ACL website for
review at: https://www.acl.gov/aboutacl/public-input.
Estimated Program Burden: Based on
DD Council reporting experience,
current data and reporting efforts
constitute approximately 238 burden
hours per grantee for a total of 1,556
hours. The table below outlines the
estimate for the hours of burden
associated with the collection of
information. Estimated Total Annual
Burden Hours: 13,328.
Responses
per respondent
Hours per
response
Total annual
burden hours
State Councils on Developmental Disabilities, Annual Program Performance
Report (PPR) ................................................................................................
DDC CDC Report ............................................................................................
DDC PHWF Report ..........................................................................................
56
56
56
1
1
1
172
52
14
9,632
2,912
784
Total ..........................................................................................................
56
........................
238
13,328
Date: September 20, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[FR Doc. 2022–20796 Filed 9–23–22; 8:45 am]
[Docket No. FDA–2022–D–0738]
BILLING CODE 4154–01–P
Ethical Considerations for Clinical
Investigations of Medical Products
Involving Children; Draft Guidance for
Industry, Sponsors, and Institutional
Review Boards; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
VerDate Sep<11>2014
16:43 Sep 23, 2022
Jkt 256001
PO 00000
Notice of availability.
Frm 00050
Fmt 4703
Sfmt 4703
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of a draft
guidance for industry, sponsors, and
institutional review boards (IRBs)
entitled ‘‘Ethical Considerations for
Clinical Investigations of Medical
Products Involving Children.’’ This draft
guidance describes FDA’s current
thinking regarding ethical
considerations for clinical investigations
of drugs, biological products, and
medical devices (collectively referred to
as ‘‘medical products’’ in this notice)
involving children. The draft guidance
is intended to assist industry, sponsors,
SUMMARY:
E:\FR\FM\26SEN1.SGM
26SEN1
]]>Agencies
[Federal Register Volume 87, Number 185 (Monday, September 26, 2022)]
[Notices]
[Pages 58356-58357]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-20796]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities: Proposed Collection;
Public Comment Request of the State Councils on Developmental
Disabilities (Councils) OMB Control Number 0985-0033
AGENCY: Administration for Community Living, Department of Health and
Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing an
opportunity for the public to comment on the proposed collection of
information listed above. Under the Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to publish a notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information, and
to allow 60 days for public comment in response to the notice. This
Information Collection (IC) Revision solicits comments on the
information collection requirements relating to the State Councils on
Developmental Disabilities (Councils) OMB control number 0985-0033.
DATES: Comments on the collection of information must be submitted
electronically by 11:59 p.m. (EST) or postmarked by November 25, 2022.
ADDRESSES: Submit electronic comments on the collection of information
to Sara Newell-Perez at [email protected]. Submit
electronic comments on the collection of information to Administration
for Community Living, 330 C Street SW, Washington, DC 20201, Attention:
Sara Newell-Perez.
FOR FURTHER INFORMATION CONTACT: Sara Newell-Perez, 202-795-7413 or
[email protected].
SUPPLEMENTARY INFORMATION: Under the 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.
``Collection of information'' is defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests or requirements that members of
the public submit reports, keep records, or provide information to a
third party. The PRA requires Federal agencies to provide a 60-day
notice in the Federal Register concerning each proposed collection of
information, including each proposed extension of an existing
collection of information, before submitting the collection to OMB for
approval. To comply with this requirement, ACL is publishing a notice
of the proposed collection of information set forth in this document.
With respect to the collection of information described below, ACL
invites comments on our burden
[[Page 58357]]
estimates or any other aspect of this collection of information,
including:
(1) whether the proposed collection of information is necessary for
the proper performance of ACL's functions, including whether the
information will have practical utility;
(2) the accuracy of ACL's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used to determine burden estimates;
(3) ways to enhance the quality, utility, and clarity of the
information to be collected; and
(4) ways to minimize the burden of the collection of information on
respondents, including through the use of automated collection
techniques when appropriate, and other forms of information technology.
The State Councils on Developmental Disabilities (Councils) are
authorized by Subtitle B of the Developmental Disabilities Assistance
and Bill of Rights Act of 2000 (DD Act), as amended, [42 U.S.C. 15001
et seq.] (The DD Act). The DD Act requires Councils to submit an annual
Program Performance Report. Section 125(c)(7) (42 U.S.C. 15025), states
that: Beginning in fiscal year 2002, the Council shall annually prepare
and transmit to the Secretary a report. Each report shall be in a form
prescribed by the Secretary by regulation under section 104(b). Each
report shall contain information about the progress made by the Council
in achieving the goals of the Council as specified in section
124(c)(4)).
The Council is responsible for the development and submission of
the PPR, and for reporting on performance measure data related to its
progress in carrying out the goals and objectives of the State Plan.
The data collected in the PPR and submitted to ACL is also used to
comply with the GPRA Modernization Act of 2010 (GPRAMA). Performance
measure results are reported to Congress under GPRAMA.
This is a revision of a currently approved information collection
that expires in 2023. To ensure the DD Council PPR is consistent with
the Executive Order on Advancing Racial Equity and Support for
Underserved Communities Through the Federal Government and the
Executive Order on Advancing Equality for Lesbian, Gay, Bisexual,
Transgender, Queer, and Intersex Individuals, ACL intends to determine
whether the sexual orientation and gender identity (SOGI) data elements
need to be adapted prior to adding them to ensure accessibility of the
questions for individuals with intellectual and developmental
disabilities.
This IC will also include elements needed to account for the
activities supported by funding from the Centers for Disease Control
and Prevention (CDC) to support access to vaccines for people with
disabilities as well as the funds awarded under the American Rescue
Plan to increase the Public Health Workforce (PHWF). All other elements
of the template remain consistent with previously approved performance
measures and corresponds to requirements in the DD Act.
The information collected from the DD Councils is used for multiple
purposes:
(1) To develop and submit at least every two years a report to the
President, Congress, and the National Council on Disability that
describes the goals and outcomes of programs supported under the DD
Act.
(2) As a tool for DD Councils to measure and report on progress in
reaching goals and identify areas for which revisions are indicated;
(3) To enhance the Federal project officers' monitoring of DD
Council progress in reaching projected outcomes;
(4) As a set of performance measures that will yield a national
portrait of DD Council program impact; and
(5) For Congress and the Administration in making funding and
appropriation decisions with regard to the DD Council program.
The proposed data collection tools may be found on the ACL website
for review at: https://www.acl.gov/about-acl/public-input.
Estimated Program Burden: Based on DD Council reporting experience,
current data and reporting efforts constitute approximately 238 burden
hours per grantee for a total of 1,556 hours. The table below outlines
the estimate for the hours of burden associated with the collection of
information. Estimated Total Annual Burden Hours: 13,328.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Total annual
Respondent/data collection activity respondents respondent response burden hours
----------------------------------------------------------------------------------------------------------------
State Councils on Developmental Disabilities, 56 1 172 9,632
Annual Program Performance Report (PPR)........
DDC CDC Report.................................. 56 1 52 2,912
DDC PHWF Report................................. 56 1 14 784
---------------------------------------------------------------
Total....................................... 56 .............. 238 13,328
----------------------------------------------------------------------------------------------------------------
Date: September 20, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2022-20796 Filed 9-23-22; 8:45 am]
BILLING CODE 4154-01-P
