Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; of the National Network of University Centers for Excellence in Developmental Disabilities Education, Research, and Service, 6744-6745 [2023-02018]
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6744
Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2023–02016 Filed 1–31–23; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
[OMB Control No. 0985–0030]
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request; of
the National Network of University
Centers for Excellence in
Developmental Disabilities Education,
Research, and Service
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 the Paperwork
Reduction Act of 1995. This 30-day
notice collects comments on the
information collection requirements
related to the National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs) OMB
control number 0985–0030.
DATES: Submit written comments on the
collection of information by March 3,
2023.
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:
Pamela O’Brien, 202–795–7417 or
pamela.obrien@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, The
Administration for Community Living
(ACL) has submitted the following
proposed collection of information to
OMB for review and clearance. ACL is
requesting approval of revisions to the
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
21:04 Jan 31, 2023
Jkt 259001
National Network of University Centers
for Excellence in Developmental
Disabilities Education, Research, and
Service OMB control number 0985–
0030. The National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs) is a
discretionary grant program that
supports the operation and
administration of UCEDDs which are
interdisciplinary education, research,
and public service units of universities
or public or not-for-profit entities
associated with universities that engage
in core functions.
This IC revision adds items to ensure
ACL is gathering the necessary and
relevant demographic information in
support of 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. The
National Academies of Science,
Engineering, and Medicine (NASEM)
recently published a report on
Measuring Sex, Gender Identity, and
Sexual Orientation for the National
Institutes of Health. This report
represents the culmination of years of
work within HHS to develop sexual
orientation and gender identity (SOGI)
data collection methodology. This IC
includes the recommended NASEM
SOGI questions.
This IC revision also includes data
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 the currently approved
UCEDD annual report.
Section 104(a) (42 U.S.C. 15004) of
the Developmental Disabilities
Assistance and Bill of Rights Act of
2000 (DD Act) directs the Secretary of
Health and Human Services to develop
and implement a system of program
accountability to monitor the grantees
funded under the DD Act of 2000. The
program accountability system must
include UCEDDs authorized under Part
D of the DD Act of 2000. Section 154(e)
(42 U.S.C. 15064) of the DD Act of 2000
includes requirements for a UCEDD
Annual Report. The UCEDD Annual
Report should contain information on
progress made in achieving the
projected goals of the Center for the
previous year, including:
PO 00000
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Fmt 4703
Sfmt 4703
(1) The extent to which the goals were
achieved;
(2) A description of the strategies that
contributed to achieving the goals;
(3) The extent goals were not
achieved, a description of factors that
impeded the achievement; and
(4) An accounting of the manner in
which funds paid to the Center under
this subtitle for a fiscal year were
expended.
In addition, the DD requires
information on proposed revisions to
the goals and a description of successful
efforts to leverage funds, other than
funds made available under the DD Act.
The DD Act also states grantees must
report on:
(1) Consumer satisfaction with the
advocacy, capacity building, and
systemic change activities of the
UCEDD;
(2) The extent to which the UCEDD’s
advocacy, capacity building, and
systemic change activities resulted in
improvements; and
(3) The extent to which collaboration
was achieved in the areas of advocacy,
capacity building, and systemic change.
Currently, UCEDDs engage in four
broad tasks: conducting
interdisciplinary training, promoting
exemplary community service programs
and providing technical assistance at all
levels from local service delivery to
community and state governments,
conducting research, and disseminating
information to the field. There are 67
UCEDDs throughout the United States
with at least one or more in every State
and Territory, as mandated.
The information derived from data
collection activities will be used for
multiple purposes:
(1) As a tool for UCEDD grantees to
measure and report on progress in
reaching goals and identify areas for
which revisions are indicated;
(2) To enhance the Federal project
officers’ monitoring of UCEDD progress
in reaching projected outcomes;
(3) To provide a set of standardized
performance measures that will yield a
national portrait of UCEDD program
impact; and
(4) For making funding and
appropriation decisions about the
UCEDD program.
The information provided in the
Annual Reports from the UCEDDs is
combined with information reported by
the State Developmental Disabilities
Councils and Protection and Advocacy
agencies to develop a biennial report.
The report describes the goals and
outcomes of programs supported under
the DD Act and is submitted to the
President, Congress, and the National
Council on Disability. The
E:\FR\FM\01FEN1.SGM
01FEN1
6745
Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices
Administration on Disabilities (AoD)
within ACL collects data via the
National Information Reporting System
(NIRS) a web-based system developed
by the Association for University
Centers on Disabilities (AUCD). The
instrument guides the development of
items to be included in NIRS for
reporting purposes.
Comments in Response to the 60-Day
Federal Register Notice
A notice published in the Federal
Register Vol 87 FR 58354 on September
26, 2022. There were zero public
comments were received during the 60day FRN.
Estimated Program Burden: ACL
estimates the burden of this collection
of information as follows: Based on
UCEDD reporting experience, current
data and reporting efforts constitute
approximately 1,462 burden hours per
grantee for a total of 97,954 annual
burden hours.
UCEDDs also worked with the
technical assistance provider to
establish burden reporting estimates for
Responses
per
respondent
Number of
respondents
Respondent/data collection activity
Hours per
response
Annual burden
hours
UCEDD Annual Report ....................................................................................
UCEDD CDC Report .......................................................................................
UCEDD PHWF Report .....................................................................................
67
67
67
1
1
1
1,462
76
18
97,954
5,092
1,206
Total ..........................................................................................................
........................
........................
........................
104,252
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2023–02018 Filed 1–31–23; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2022–N–1894]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Yale-Mayo Clinic
Centers of Excellence in Regulatory
Science and Innovation B12 Pediatric
Device Survey
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
DATES: Submit written comments
(including recommendations) on the
collection of information by March 3,
2023.
ADDRESSES: To ensure that comments on
the information collection are received,
OMB recommends that written
comments be submitted to https://
www.reginfo.gov/public/do/PRAMain.
Find this particular information
SUMMARY:
lotter on DSK11XQN23PROD with NOTICES1
Centers for Disease Control (CDC) and
Public Health Workforce (PHWF)
reporting. It should be noted that not all
UCEDDs chose to accept CDC and
PHWF funds. The CDC and PHWF
reporting totals 6,298 annual burden
hours. The overall estimated total
annual burden hours factoring in all
three reports is: 104,252.
Estimated Total Annual Burden
Hours: 104,252.
VerDate Sep<11>2014
21:04 Jan 31, 2023
Jkt 259001
collection by selecting ‘‘Currently under
Review—Open for Public Comments’’ or
by using the search function. The title
of this information collection is ‘‘YaleMayo Clinic Centers of Excellence in
Regulatory Science and Innovation B12
Pediatric Device Survey.’’ Also include
the FDA docket number found in
brackets in the heading of this
document.
FOR FURTHER INFORMATION CONTACT:
JonnaLynn Capezzuto, Office of
Operations, Food and Drug
Administration, Three White Flint
North, 10A–12M, 11601 Landsdown St.,
North Bethesda, MD 20852, 301–796–
3794, PRAStaff@fda.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
Yale-Mayo Clinic Centers of Excellence
in Regulatory Science and Innovation
(CERSI) B12 Pediatric Device Survey
OMB Control Number 0910–NEW
Despite numerous legislative,
regulatory, and scientific efforts, there
has been little change in the number of
devices approved for use in pediatric
patients. This has often led to devices
being adapted for use in children
without an appropriate level of
evidence, exposing them to inconsistent
benefit risk profiles. This health
inequity highlights the need for devices
that are designed, evaluated, and
labelled for pediatric patients. To
address these challenges, this collection
is being done to survey industry and
other key stakeholders in the medical
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Fmt 4703
Sfmt 4703
device ecosystem to identify the barriers
that prevent product developers from
entering the pediatric device market as
well as the proper incentives that would
motivate them to innovate and sustain
within this market.
This survey is a followup to the
public meeting that FDA held in August
2018, entitled ‘‘Pediatric Medical Device
Development.’’ As mandated by section
502(d) of the FDA Reauthorization Act
of 2017 (Pub. L. 115–52), the meeting
was convened to address several topics,
including consideration of ways to: (1)
increase FDA assistance to medical
device manufacturers in developing
devices for pediatric populations that
are approved or cleared, and labeled, for
their use and (2) identify current
barriers to pediatric device development
and incentives to address such barriers.
Feedback from this meeting clarified
the need to better understand factors
influencing suboptimal engagement and
participation by diverse innovators in
the pediatric medical device space.
Information garnered from this survey
may help inform strategic plans to
optimize existing programs for the
needs of pediatric medical device
innovators and develop new programs
that will support sustained development
in this space.
In the Federal Register of September
23, 2022 (87 FR 58106), FDA published
a 60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
E:\FR\FM\01FEN1.SGM
01FEN1
]]>Agencies
[Federal Register Volume 88, Number 21 (Wednesday, February 1, 2023)]
[Notices]
[Pages 6744-6745]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-02018]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
[OMB Control No. 0985-0030]
Agency Information Collection Activities; Submission for OMB
Review; Public Comment Request; of the National Network of University
Centers for Excellence in Developmental Disabilities Education,
Research, and Service
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 the Paperwork Reduction Act of 1995. This 30-day notice
collects comments on the information collection requirements related to
the National Network of University Centers for Excellence in
Developmental Disabilities Education, Research, and Service (UCEDDs)
OMB control number 0985-0030.
DATES: Submit written comments on the collection of information by
March 3, 2023.
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: Pamela O'Brien, 202-795-7417 or
[email protected].
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, The
Administration for Community Living (ACL) has submitted the following
proposed collection of information to OMB for review and clearance. ACL
is requesting approval of revisions to the National Network of
University Centers for Excellence in Developmental Disabilities
Education, Research, and Service OMB control number 0985-0030. The
National Network of University Centers for Excellence in Developmental
Disabilities Education, Research, and Service (UCEDDs) is a
discretionary grant program that supports the operation and
administration of UCEDDs which are interdisciplinary education,
research, and public service units of universities or public or not-
for-profit entities associated with universities that engage in core
functions.
This IC revision adds items to ensure ACL is gathering the
necessary and relevant demographic information in support of 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. The National Academies of Science, Engineering,
and Medicine (NASEM) recently published a report on Measuring Sex,
Gender Identity, and Sexual Orientation for the National Institutes of
Health. This report represents the culmination of years of work within
HHS to develop sexual orientation and gender identity (SOGI) data
collection methodology. This IC includes the recommended NASEM SOGI
questions.
This IC revision also includes data 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 the currently approved
UCEDD annual report.
Section 104(a) (42 U.S.C. 15004) of the Developmental Disabilities
Assistance and Bill of Rights Act of 2000 (DD Act) directs the
Secretary of Health and Human Services to develop and implement a
system of program accountability to monitor the grantees funded under
the DD Act of 2000. The program accountability system must include
UCEDDs authorized under Part D of the DD Act of 2000. Section 154(e)
(42 U.S.C. 15064) of the DD Act of 2000 includes requirements for a
UCEDD Annual Report. The UCEDD Annual Report should contain information
on progress made in achieving the projected goals of the Center for the
previous year, including:
(1) The extent to which the goals were achieved;
(2) A description of the strategies that contributed to achieving
the goals;
(3) The extent goals were not achieved, a description of factors
that impeded the achievement; and
(4) An accounting of the manner in which funds paid to the Center
under this subtitle for a fiscal year were expended.
In addition, the DD requires information on proposed revisions to
the goals and a description of successful efforts to leverage funds,
other than funds made available under the DD Act.
The DD Act also states grantees must report on:
(1) Consumer satisfaction with the advocacy, capacity building, and
systemic change activities of the UCEDD;
(2) The extent to which the UCEDD's advocacy, capacity building,
and systemic change activities resulted in improvements; and
(3) The extent to which collaboration was achieved in the areas of
advocacy, capacity building, and systemic change.
Currently, UCEDDs engage in four broad tasks: conducting
interdisciplinary training, promoting exemplary community service
programs and providing technical assistance at all levels from local
service delivery to community and state governments, conducting
research, and disseminating information to the field. There are 67
UCEDDs throughout the United States with at least one or more in every
State and Territory, as mandated.
The information derived from data collection activities will be
used for multiple purposes:
(1) As a tool for UCEDD grantees to measure and report on progress
in reaching goals and identify areas for which revisions are indicated;
(2) To enhance the Federal project officers' monitoring of UCEDD
progress in reaching projected outcomes;
(3) To provide a set of standardized performance measures that will
yield a national portrait of UCEDD program impact; and
(4) For making funding and appropriation decisions about the UCEDD
program.
The information provided in the Annual Reports from the UCEDDs is
combined with information reported by the State Developmental
Disabilities Councils and Protection and Advocacy agencies to develop a
biennial report. The report describes the goals and outcomes of
programs supported under the DD Act and is submitted to the President,
Congress, and the National Council on Disability. The
[[Page 6745]]
Administration on Disabilities (AoD) within ACL collects data via the
National Information Reporting System (NIRS) a web-based system
developed by the Association for University Centers on Disabilities
(AUCD). The instrument guides the development of items to be included
in NIRS for reporting purposes.
Comments in Response to the 60-Day Federal Register Notice
A notice published in the Federal Register Vol 87 FR 58354 on
September 26, 2022. There were zero public comments were received
during the 60-day FRN.
Estimated Program Burden: ACL estimates the burden of this
collection of information as follows: Based on UCEDD reporting
experience, current data and reporting efforts constitute approximately
1,462 burden hours per grantee for a total of 97,954 annual burden
hours.
UCEDDs also worked with the technical assistance provider to
establish burden reporting estimates for Centers for Disease Control
(CDC) and Public Health Workforce (PHWF) reporting. It should be noted
that not all UCEDDs chose to accept CDC and PHWF funds. The CDC and
PHWF reporting totals 6,298 annual burden hours. The overall estimated
total annual burden hours factoring in all three reports is: 104,252.
Estimated Total Annual Burden Hours: 104,252.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Annual burden
Respondent/data collection activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
UCEDD Annual Report............................. 67 1 1,462 97,954
UCEDD CDC Report................................ 67 1 76 5,092
UCEDD PHWF Report............................... 67 1 18 1,206
---------------------------------------------------------------
Total....................................... .............. .............. .............. 104,252
----------------------------------------------------------------------------------------------------------------
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2023-02018 Filed 1-31-23; 8:45 am]
BILLING CODE 4154-01-P
