Agency Information Collection Activities; Proposed Collection; Public Comment Request; Generic Information Collection Request for Health Resources and Services Administration Stakeholder Gatherings, 83694-83695 [2024-23875]
Download as PDF
<![CDATA[
83694
Federal Register / Vol. 89, No. 201 / Thursday, October 17, 2024 / Notices
Dated: October 9, 2024.
Eric Flamm,
Acting Associate Commissioner for Policy.
[FR Doc. 2024–23967 Filed 10–16–24; 8:45 am]
BILLING CODE 4164–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request; Generic
Information Collection Request for
Health Resources and Services
Administration Stakeholder Gatherings
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In compliance with the
Paperwork Reduction Act of 1995,
HRSA 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.
SUMMARY:
Comments on this ICR should be
received no later than November 18,
2024.
DATES:
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
Joella Roland, the HRSA Information
Collection Clearance Officer, at
paperwork@hrsa.gov or call (301) 443–
3983.
SUPPLEMENTARY INFORMATION:
Information Collection Request Title:
Umbrella Generic Information
Collection Request for Information
Collections Related to HRSA Gatherings,
OMB No. 0906–xxxx—New.
Abstract: HRSA conducts gatherings
for various purposes, including
conferences, meetings, workshops,
ddrumheller on DSK120RN23PROD with NOTICES1
ADDRESSES:
VerDate Sep<11>2014
18:31 Oct 16, 2024
Jkt 265001
webinars, trainings, communities of
practice, focus groups, and other inperson or virtual gatherings for
individuals and organizations that are
interested in HRSA programs. To ensure
that HRSA has sufficient information to
plan, convene, administer, and evaluate
the effectiveness of these gatherings,
HRSA must collect information from
potential attendees, such as contact
information, organizational information,
logistical information (e.g., preferred
delivery methods), accommodation
needs, and feedback about the
gathering’s content. Furthermore, HRSA
may conduct a test of knowledge to see
what attendees know about the subject
matter before or during the meeting or
focus group. After the gathering
concludes, attendees may be asked to
complete an evaluation form and/or a
test of knowledge to measure the
gathering’s effectiveness. In some
instances, attendees may also apply
and/or submit an abstract for
prescreening to be selected for
attendance.
An illustrative, but not exhaustive,
list of examples of standardized
information collection activities related
to HRSA gatherings include:
• Registration Forms: Information
collected includes name, contact
information, organization/affiliation,
demographic information (age, race or
ethnicity, occupation, and location), and
attendee accommodation needs.
• Application Forms for panels,
posters, or other presentation formats:
For application forms, information
collected also includes title, author(s),
organization/affiliation, and
presentation abstract, in addition to the
information contained in the
registration form.
• Focus Groups: Information
collected includes attendee/presenter
responses to standard questions
regarding topics posed to smaller groups
during HRSA gatherings.
• Pre-/Post-gathering Forms:
Information collected includes attendee/
presenter preferences, feedback, pre-/
post-meeting questions, and tests of
knowledge in response to standard
questions.
A 60-day notice published in the
Federal Register on June 21, 2024, 89
FR 52067–68. HRSA received one
comment that was outside the scope of
the proposed information collection.
Need and Proposed Use of the
Information: The purpose of collections
under this umbrella generic information
collection is to gather appropriate
information to plan, administer, and
evaluate HRSA gatherings. While HRSA
can evaluate the general need for and
the overall practical utility of such
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
information collection in advance,
HRSA may not be able to determine the
details of the specific individual
collections until a later time. The
planning for these gatherings is often on
a quick timeline and the standard
timeline to comply with a full request
under the Paperwork Reduction Act
could inhibit HRSA’s ability to collect
information to inform these activities.
The information collected is expected to
be voluntary, low-burden, and
uncontroversial. Therefore, an umbrella
generic is requested to allow for quick
turnaround requests for similar
information collections related to these
activities.
As this Generic ICR for HRSA
Stakeholder Gatherings will focus on
the awareness, understanding, attitudes,
preferences, or experiences of HRSA
customers or other stakeholders (e.g.,
funding recipients and their delivery
partners, potential funding applicants)
relating to existing or future services,
products, or communication materials,
the Fast Track Process should apply to
this information collection. Therefore,
HRSA requests OMB provide a response
on individual generic information
collections within 5 business days.
Likely Respondents: Attendees and
presenters at HRSA conferences,
meetings, workshops, webinars,
trainings, communities of practice, and
other in-person, virtual, or hybrid
gatherings. Attendees and presenters
may include HRSA funding recipients,
individuals seeking to participate in a
HRSA-funded program, members of the
public who utilize HRSA-funded
resources, contractors, researchers, and
other members of the public. Responses
to any information collections under
this Generic ICR for HRSA Stakeholder
Gatherings are not required to obtain or
retain any benefit.
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. HRSA
conducted this estimate based on
reviewing burden estimates of forms
E:\FR\FM\17OCN1.SGM
17OCN1
83695
Federal Register / Vol. 89, No. 201 / Thursday, October 17, 2024 / Notices
from previous HRSA gatherings, which
were approved under other Umbrella or
Regular packages.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Form name
Total
responses
Average
burden per
response
(in hours)
Total
burden hours
Registration Forms ...............................................................
Applications ..........................................................................
Pre- and Post-Gathering Forms ..........................................
Focus Groups ......................................................................
100,000
10,000
200,000
100,000
1
1
1
3
100,000
10,000
200,000
300,000
0.5
1.0
0.5
3.0
50,000
10,000
100,000
900,000
Total ..............................................................................
410,000
........................
610,000
........................
1,060,000
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024–23875 Filed 10–16–24; 8:45 am]
BILLING CODE 4165–15–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Center for Scientific Review; Notice of
Closed Meetings
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of the
following meetings.
The meetings will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
responses per
respondent
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Topics in
Viral Pathogenesis and Immunity.
Date: November 1, 2024.
Time: 9:30 a.m. to 11:00 a.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Neerja Kaushik-Basu,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3198,
MSC 7808, Bethesda, MD 20892, (301) 435–
1742, kaushikbasun@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; PAR Panel:
Fogarty International Research Training.
Date: November 7, 2024.
Time: 2:00 p.m. to 4:00 p.m.
Agenda: To review and evaluate grant
applications.
VerDate Sep<11>2014
18:31 Oct 16, 2024
Jkt 265001
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Aruna K. Behera, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 4211,
MSC 7814, Bethesda, MD 20892, (301) 435–
6809, beheraak@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Small
Business: Cell and Molecular Biology.
Date: November 12–13, 2024.
Time: 9:00 a.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Megan L. Goodall, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Bethesda, MD
20892, (301) 594–8334, megan.goodall@
nih.gov.
Name of Committee: Population Sciences
and Epidemiology Integrated Review Group;
Cardiovascular and Respiratory Diseases
Study Section.
Date: November 13–14, 2024.
Time: 9:00 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: In Person and Virtual
Meeting.
Contact Person: Raquel L. Velazquezkronen, Ph.D., Scientific Review Officer,
Center for Scientific Review, National
Institutes of Health, 6701 Rockledge Dr.,
Bethesda, MD 20892, (513) 301–9047,
velazquezrl@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Program
Project—Biopsychosocial Mechanisms of
Substance Use after Bariatric Surgery.
Date: November 13, 2024.
Time: 1:00 p.m. to 6:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
Meeting Format: Virtual Meeting.
Contact Person: Sara Louise Hargrave,
Ph.D., Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 3170,
Bethesda, MD 20892, (301) 443–7193,
hargravesl@mail.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Member
Conflict: Cell and Developmental Biology of
Eye.
Date: November 13, 2024.
Time: 2:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Rass M. Shayiq, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Drive, Room 2182,
MSC 7818, Bethesda, MD 20892, (301) 435–
2359, shayiqr@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel;
Fellowships: Sensory and Motor
Neurosciences, Cognition and Perception.
Date: November 14–15, 2024.
Time: 8:00 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: National Institutes of Health,
Rockledge II, 6701 Rockledge Drive,
Bethesda, MD 20892.
Meeting Format: Virtual Meeting.
Contact Person: Simon Peter Peron, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
Health, 6701 Rockledge Dr., Room 1009K,
Bethesda, MD 20892, (301) 594–6236,
peronsp@csr.nih.gov.
Name of Committee: Center for Scientific
Review Special Emphasis Panel; Small
Business: Cardiovascular Sciences Activities.
Date: November 14–15, 2024.
Time: 8:00 a.m. to 8:00 p.m.
Agenda: To review and evaluate grant
applications.
Address: Hilton Garden Inn Bethesda
Downtown, 7301 Waverly Street, Bethesda,
MD 20814.
Meeting Format: In Person.
Contact Person: Dmitri V. Gnatenko, Ph.D.,
Scientific Review Officer, Center for
Scientific Review, National Institutes of
E:\FR\FM\17OCN1.SGM
17OCN1
]]>Agencies
[Federal Register Volume 89, Number 201 (Thursday, October 17, 2024)]
[Notices]
[Pages 83694-83695]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-23875]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities; Proposed Collection;
Public Comment Request; Generic Information Collection Request for
Health Resources and Services Administration Stakeholder Gatherings
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the Paperwork Reduction Act of 1995, HRSA
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 November
18, 2024.
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 Joella Roland, the HRSA
Information Collection Clearance Officer, at [email protected] or call
(301) 443-3983.
SUPPLEMENTARY INFORMATION: Information Collection Request Title:
Umbrella Generic Information Collection Request for Information
Collections Related to HRSA Gatherings, OMB No. 0906-xxxx--New.
Abstract: HRSA conducts gatherings for various purposes, including
conferences, meetings, workshops, webinars, trainings, communities of
practice, focus groups, and other in-person or virtual gatherings for
individuals and organizations that are interested in HRSA programs. To
ensure that HRSA has sufficient information to plan, convene,
administer, and evaluate the effectiveness of these gatherings, HRSA
must collect information from potential attendees, such as contact
information, organizational information, logistical information (e.g.,
preferred delivery methods), accommodation needs, and feedback about
the gathering's content. Furthermore, HRSA may conduct a test of
knowledge to see what attendees know about the subject matter before or
during the meeting or focus group. After the gathering concludes,
attendees may be asked to complete an evaluation form and/or a test of
knowledge to measure the gathering's effectiveness. In some instances,
attendees may also apply and/or submit an abstract for prescreening to
be selected for attendance.
An illustrative, but not exhaustive, list of examples of
standardized information collection activities related to HRSA
gatherings include:
Registration Forms: Information collected includes name,
contact information, organization/affiliation, demographic information
(age, race or ethnicity, occupation, and location), and attendee
accommodation needs.
Application Forms for panels, posters, or other
presentation formats: For application forms, information collected also
includes title, author(s), organization/affiliation, and presentation
abstract, in addition to the information contained in the registration
form.
Focus Groups: Information collected includes attendee/
presenter responses to standard questions regarding topics posed to
smaller groups during HRSA gatherings.
Pre-/Post-gathering Forms: Information collected includes
attendee/presenter preferences, feedback, pre-/post-meeting questions,
and tests of knowledge in response to standard questions.
A 60-day notice published in the Federal Register on June 21, 2024,
89 FR 52067-68. HRSA received one comment that was outside the scope of
the proposed information collection.
Need and Proposed Use of the Information: The purpose of
collections under this umbrella generic information collection is to
gather appropriate information to plan, administer, and evaluate HRSA
gatherings. While HRSA can evaluate the general need for and the
overall practical utility of such information collection in advance,
HRSA may not be able to determine the details of the specific
individual collections until a later time. The planning for these
gatherings is often on a quick timeline and the standard timeline to
comply with a full request under the Paperwork Reduction Act could
inhibit HRSA's ability to collect information to inform these
activities. The information collected is expected to be voluntary, low-
burden, and uncontroversial. Therefore, an umbrella generic is
requested to allow for quick turnaround requests for similar
information collections related to these activities.
As this Generic ICR for HRSA Stakeholder Gatherings will focus on
the awareness, understanding, attitudes, preferences, or experiences of
HRSA customers or other stakeholders (e.g., funding recipients and
their delivery partners, potential funding applicants) relating to
existing or future services, products, or communication materials, the
Fast Track Process should apply to this information collection.
Therefore, HRSA requests OMB provide a response on individual generic
information collections within 5 business days.
Likely Respondents: Attendees and presenters at HRSA conferences,
meetings, workshops, webinars, trainings, communities of practice, and
other in-person, virtual, or hybrid gatherings. Attendees and
presenters may include HRSA funding recipients, individuals seeking to
participate in a HRSA-funded program, members of the public who utilize
HRSA-funded resources, contractors, researchers, and other members of
the public. Responses to any information collections under this Generic
ICR for HRSA Stakeholder Gatherings are not required to obtain or
retain any benefit.
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. HRSA conducted this
estimate based on reviewing burden estimates of forms
[[Page 83695]]
from previous HRSA gatherings, which were approved under other Umbrella
or Regular packages.
Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Form name Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Registration Forms.............. 100,000 1 100,000 0.5 50,000
Applications.................... 10,000 1 10,000 1.0 10,000
Pre- and Post-Gathering Forms... 200,000 1 200,000 0.5 100,000
Focus Groups.................... 100,000 3 300,000 3.0 900,000
-------------------------------------------------------------------------------
Total....................... 410,000 .............. 610,000 .............. 1,060,000
----------------------------------------------------------------------------------------------------------------
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024-23875 Filed 10-16-24; 8:45 am]
BILLING CODE 4165-15-P
