Proposed Collection; 60-Day Comment Request; Application and Impact of Clinical Research Training on Healthcare Professionals in Academia and Clinical Research (Office of the Director), 49472-49473 [2023-16184]
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Federal Register / Vol. 88, No. 145 / Monday, July 31, 2023 / Notices
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Neurological Disorders and Stroke Special
Emphasis Panel; Phase 2 Clinical Trials in
Neurology.
Date: August 14, 2023.
Time: 3:00 p.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Institutes of Health,
Neuroscience Center, 6001 Executive
Boulevard, Rockville, MD 20852 (Virtual
Meeting).
Contact Person: Iqbal Sayeed, Scientific
Review Officer, Scientific Review Branch,
Division of Extramural Activities, NINDS/
NIH NSC, 6001 Executive Blvd., Suite 3208,
MSC 9529, Rockville, MD 20852, 301–496–
9223, iqbal.sayeed@nih.gov.
This notice is being published less than 15
days prior to the meeting due to the timing
limitations imposed by the review and
funding cycle.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.853, Clinical Research
Related to Neurological Disorders; 93.854,
Biological Basis Research in the
Neurosciences, National Institutes of Health,
HHS.)
Dated: July 25, 2023.
Tyeshia M. Roberson-Curtis,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2023–16134 Filed 7–28–23; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment
Request; Application and Impact of
Clinical Research Training on
Healthcare Professionals in Academia
and Clinical Research (Office of the
Director)
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
In compliance with the
requirement of the Paperwork
Reduction Act of 1995 to provide
opportunity for public comment on
SUMMARY:
proposed data collection projects, the
Office of Clinical Research Education,
Collaboration, and Outreach (OCRECO),
Office of the Director (OD), National
Institutes of Health, will publish
periodic summaries of proposed
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 60 days of the date of this
publication.
FOR FURTHER INFORMATION CONTACT: To
obtain a copy of the data collection
plans and instruments, submit
comments in writing, or request more
information on the proposed project,
contact: Dr. Anne Zajicek, M.D.,
Pharm.D., Program Director, Office of
Clinical Research Education,
Collaboration, and Outreach, NIH Office
of the Director, Building 1, Room 201,
MSC–0155, Bethesda, Maryland 20892
or call non-toll-free number (301) 480–
9913 or email your request, including
your address to: zajiceka@mail.nih.gov.
Formal requests for additional plans and
instruments must be requested in
writing.
SUPPLEMENTARY INFORMATION: Section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: written
comments and/or suggestions from the
public and affected agencies are invited
to address one or more of the following
points: (1) Whether the proposed
collection of information is necessary
for the proper performance of the
function of the agency, including
whether the information will have
practical utility; (2) The accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
Ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) Ways to minimizes
the burden of the collection of
information on those who are to
respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
Proposed Collection Title:
Application and Impact of Clinical
Research Training on Healthcare
Professionals in Academia and Clinical
Research, 0925–0764, exp., date 02/28/
2026, Revision Office of Clinical
Research Education and Collaboration
Outreach (OCRECO), National Institutes
of Health (NIH), Office of the Director
(OD).
Need and Use of Information
Collection: The purpose of this revision
is to: update the name of the office
responsible for these on-line training
programs (from Office of Clinical
Research to Office of Clinical Research
Education and Collaboration Outreach);
revise the course evaluation survey
questions; add an additional on-line
course, ‘‘Ethical and Regulatory Aspects
of Clinical Research’’; change the course
opening and close dates from Oct–June
to Sept–July. The survey will continue
to assess the long-term impact and
outcomes of clinical research training
programs provided by the newly formed
Office of Clinical Research Education,
Collaboration, and Outreach (previously
the Office of Clinical Research) located
in the NIH Office of the Director (OD)
over a ten-year follow-up period. The
information received from respondents
will provide insight on the following:
impact of the courses on (a) promotion
of professional competence, (b) research
productivity and independence, and (c)
future career development within
clinical, translational, and academic
research settings. These surveys will
provide preliminary data and guidance
in (1) developing recommendations for
collecting outcomes to assess the
effectiveness of the training courses, and
(2) tracking the impact of the
curriculum on participants’ ability to
perform successfully in academic, nonacademic, research, and non-research
settings.
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
820.
ddrumheller on DSK120RN23PROD with NOTICES1
ESTIMATED ANNUALIZED BURDEN HOURS
Form name
Type of respondents
OCRECO Learning Portal Registration (Attachment 1) ............................
Healthcare Professionals ........
Students ..................................
General Public ........................
Healthcare Professionals ........
Students ..................................
General Public ........................
Healthcare Professionals ........
Students ..................................
IPPCR Lecture Evaluation (Attachment 2) ................................................
IPPCR Final Course Evaluation(Attachment 4) ........................................
VerDate Sep<11>2014
18:11 Jul 28, 2023
Jkt 259001
PO 00000
Frm 00039
Fmt 4703
Sfmt 4703
Estimated
number of
respondents
E:\FR\FM\31JYN1.SGM
Number of
responses per
respondent
2000
1000
500
750
500
250
750
500
31JYN1
1
1
1
1
1
1
1
1
Average
burden per
response
(in hours)
5/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
Total
annual
burden
hours
167
83
42
63
42
21
63
42
49473
Federal Register / Vol. 88, No. 145 / Monday, July 31, 2023 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS—Continued
Form name
Type of respondents
PCP Lecture Evaluation (Attachment 3) ...................................................
PCP Final Course Evaluation (Attachment 5) ...........................................
NIH Summer Course in Clinical and Translational Research Course
Evaluation (Attachment 6).
Sabbatical in Clinical Research Management Course Evaluation (Attachment 7).
Ethical and Regulatory Aspects of Clinical Research (Asynchronous/Online) Course (Attachment 8).
Total ....................................................................................................
Dated: July 25, 2023.
Tara A. Schwetz,
Acting Principal Deputy Director, National
Institutes of Health.
[FR Doc. 2023–16184 Filed 7–28–23; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
ddrumheller on DSK120RN23PROD with NOTICES1
National Human Genome Research
Institute; Notice of Meeting
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the National Advisory
Council for Human Genome Research.
This is a hybrid meeting held inperson and virtually and is open to the
public as indicated below. Individuals
who plan to attend in-person or view
the virtual meeting and need special
assistance or other reasonable
accommodations, should notify the
Contact Person listed below in advance
of the meeting. The meeting will be
videocast and can be accessed from
https://www.genome.gov/about-nhgri/
Institute-Advisors/National-AdvisoryCouncil-for-Human-Genome-Research.
The meeting 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.
VerDate Sep<11>2014
18:11 Jul 28, 2023
Jkt 259001
Estimated
number of
respondents
Frm 00040
Average
burden per
response
(in hours)
Total
annual
burden
hours
General Public ........................
Healthcare Professionals ........
Students ..................................
General Public ........................
Healthcare Professionals ........
Students ..................................
General Public ........................
Healthcare Professionals ........
250
750
500
250
750
500
250
20
1
1
1
1
1
1
1
1
5/60
5/60
5/60
5/60
5/60
5/60
5/60
5/60
21
63
42
21
63
42
21
2
Healthcare Professionals ........
20
1
5/60
2
Healthcare Professionals ........
Students ..................................
General Public ........................
100
50
100
1
1
1
5/60
5/60
5/60
8
4
8
.................................................
........................
9,790
....................
820
Name of Committee: National Advisory
Council for Human Genome Research.
Date: September 18–19, 2023.
Closed: September 18, 2023, 9:00 a.m. to
10:00 a.m.
Agenda: To review and evaluate grant
applications.
Place: National Human Genome Research
Institute, National Institutes of Health, 6700B
Rockledge Drive, Suite 1100, Bethesda, MD
20892.
Open: September 18, 2023, 10:30 a.m. to
6:30 p.m.
Agenda: Report of Institute Director and
Institute Staff.
Place: National Human Genome Research
Institute, 6700B Rockledge Drive, Suite 1100,
Bethesda, MD 20892.
Closed: September 19, 2023, 10:00 a.m. to
5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: National Human Genome Research
Institute, National Institutes of Health, 6700B
Rockledge Drive, Suite 1100, Bethesda, MD
20892.
Contact Person: Rudy O. Pozzatti, Ph.D.,
Scientific Review Officer, Scientific Review
Branch, National Human Genome Research
Institute, 6700B Rockledge Drive, Suite 1100,
Rockville, MD 20892, (301) 402–0838,
pozzattr@mail.nih.gov.
Any interested person may file written
comments with the committee within 15
days after the meeting by forwarding the
statement to the Contact Person listed on this
notice. The statement should include the
name, address, telephone number and when
applicable, the business or professional
affiliation of the interested person.
Information is also available on the
Institute’s/Center’s home page: https://
www.genome.gov/council, where an agenda
and any additional information for the
meeting will be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.172, Human Genome
Research, National Institutes of Health, HHS)
PO 00000
Number of
responses per
respondent
Fmt 4703
Sfmt 4703
Dated: July 26, 2023.
Melanie J. Pantoja,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2023–16147 Filed 7–28–23; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Submission for OMB Review; 30-Day
Comment Request; Generic Clearance
for NIH Citizen Science and
Crowdsourcing Projects (Office of the
Director)
AGENCY:
National Institutes of Health,
HHS.
ACTION:
Notice.
In compliance with the
Paperwork Reduction Act of 1995, the
National Institutes of Health (NIH) has
submitted to the Office of Management
and Budget (OMB) a request for review
and approval of the information
collection listed below.
DATES: Comments regarding this
information collection are best assured
of having their full effect if received
within 30-days of the date of this
publication.
SUMMARY:
Written comments and/or
suggestions regarding the item(s)
contained in this notice, especially
regarding the estimated public burden
and associated response time, should be
directed to the: Office of Management
and Budget, Office of Regulatory Affairs,
OIRA_submission@omb.eop.gov or by
fax to 202–395–6974, Attention: Desk
Officer for NIH.
FOR FURTHER INFORMATION CONTACT: To
request more information on the
proposed project or to obtain a copy of
ADDRESSES:
E:\FR\FM\31JYN1.SGM
31JYN1
]]>Agencies
[Federal Register Volume 88, Number 145 (Monday, July 31, 2023)]
[Notices]
[Pages 49472-49473]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-16184]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request; Application and
Impact of Clinical Research Training on Healthcare Professionals in
Academia and Clinical Research (Office of the Director)
AGENCY: National Institutes of Health, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement of the Paperwork Reduction
Act of 1995 to provide opportunity for public comment on proposed data
collection projects, the Office of Clinical Research Education,
Collaboration, and Outreach (OCRECO), Office of the Director (OD),
National Institutes of Health, will publish periodic summaries of
proposed projects to be submitted to the Office of Management and
Budget (OMB) for review and approval.
DATES: Comments regarding this information collection are best assured
of having their full effect if received within 60 days of the date of
this publication.
FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data
collection plans and instruments, submit comments in writing, or
request more information on the proposed project, contact: Dr. Anne
Zajicek, M.D., Pharm.D., Program Director, Office of Clinical Research
Education, Collaboration, and Outreach, NIH Office of the Director,
Building 1, Room 201, MSC-0155, Bethesda, Maryland 20892 or call non-
toll-free number (301) 480-9913 or email your request, including your
address to: [email protected]. Formal requests for additional plans
and instruments must be requested in writing.
SUPPLEMENTARY INFORMATION: Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995 requires: written comments and/or suggestions
from the public and affected agencies are invited to address one or
more of the following points: (1) Whether the proposed collection of
information is necessary for the proper performance of the function of
the agency, including whether the information will have practical
utility; (2) The accuracy of the agency's estimate of the burden of the
proposed collection of information, including the validity of the
methodology and assumptions used; (3) Ways to enhance the quality,
utility, and clarity of the information to be collected; and (4) Ways
to minimizes the burden of the collection of information on those who
are to respond, including the use of appropriate automated, electronic,
mechanical, or other technological collection techniques or other forms
of information technology.
Proposed Collection Title: Application and Impact of Clinical
Research Training on Healthcare Professionals in Academia and Clinical
Research, 0925-0764, exp., date 02/28/2026, Revision Office of Clinical
Research Education and Collaboration Outreach (OCRECO), National
Institutes of Health (NIH), Office of the Director (OD).
Need and Use of Information Collection: The purpose of this
revision is to: update the name of the office responsible for these on-
line training programs (from Office of Clinical Research to Office of
Clinical Research Education and Collaboration Outreach); revise the
course evaluation survey questions; add an additional on-line course,
``Ethical and Regulatory Aspects of Clinical Research''; change the
course opening and close dates from Oct-June to Sept-July. The survey
will continue to assess the long-term impact and outcomes of clinical
research training programs provided by the newly formed Office of
Clinical Research Education, Collaboration, and Outreach (previously
the Office of Clinical Research) located in the NIH Office of the
Director (OD) over a ten-year follow-up period. The information
received from respondents will provide insight on the following: impact
of the courses on (a) promotion of professional competence, (b)
research productivity and independence, and (c) future career
development within clinical, translational, and academic research
settings. These surveys will provide preliminary data and guidance in
(1) developing recommendations for collecting outcomes to assess the
effectiveness of the training courses, and (2) tracking the impact of
the curriculum on participants' ability to perform successfully in
academic, non-academic, research, and non-research settings.
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 820.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average Total
Estimated Number of burden per annual
Form name Type of respondents number of responses per response burden
respondents respondent (in hours) hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
OCRECO Learning Portal Registration Healthcare Professionals......................... 2000 1 5/60 167
(Attachment 1).
Students......................................... 1000 1 5/60 83
General Public................................... 500 1 5/60 42
IPPCR Lecture Evaluation (Attachment 2)....... Healthcare Professionals......................... 750 1 5/60 63
Students......................................... 500 1 5/60 42
General Public................................... 250 1 5/60 21
IPPCR Final Course Evaluation(Attachment 4)... Healthcare Professionals......................... 750 1 5/60 63
Students......................................... 500 1 5/60 42
[[Page 49473]]
General Public................................... 250 1 5/60 21
PCP Lecture Evaluation (Attachment 3)......... Healthcare Professionals......................... 750 1 5/60 63
Students......................................... 500 1 5/60 42
General Public................................... 250 1 5/60 21
PCP Final Course Evaluation (Attachment 5).... Healthcare Professionals......................... 750 1 5/60 63
Students......................................... 500 1 5/60 42
General Public................................... 250 1 5/60 21
NIH Summer Course in Clinical and Healthcare Professionals......................... 20 1 5/60 2
Translational Research Course Evaluation
(Attachment 6).
Sabbatical in Clinical Research Management Healthcare Professionals......................... 20 1 5/60 2
Course Evaluation (Attachment 7).
Ethical and Regulatory Aspects of Clinical Healthcare Professionals......................... 100 1 5/60 8
Research (Asynchronous/Online) Course Students......................................... 50 1 5/60 4
(Attachment 8). General Public................................... 100 1 5/60 8
------------------------------------------------------
Total..................................... ................................................. .............. 9,790 ........... 820
--------------------------------------------------------------------------------------------------------------------------------------------------------
Dated: July 25, 2023.
Tara A. Schwetz,
Acting Principal Deputy Director, National Institutes of Health.
[FR Doc. 2023-16184 Filed 7-28-23; 8:45 am]
BILLING CODE 4140-01-P
