Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 79626-79627 [2024-22291]
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Federal Register / Vol. 89, No. 189 / Monday, September 30, 2024 / Notices
practices regulation (21 CFR 10.115).
The guidance represents the current
thinking of FDA on ‘‘Clarification of
Radiation Control Regulations for
Manufacturers of Diagnostic X-Ray
Equipment.’’ It does not establish any
rights for any person and is not binding
on FDA or the public. You can use an
alternative approach if it satisfies the
requirements of the applicable statutes
and regulations.
II. Electronic Access
Persons interested in obtaining a copy
of the guidance may do so by
downloading an electronic copy from
the internet. A search capability for all
Center for Devices and Radiological
Health guidance documents is available
at https://www.fda.gov/medical-devices/
device-advice-comprehensiveregulatory-assistance/guidancedocuments-medical-devices-andradiation-emitting-products. This
guidance document is also available at
https://www.regulations.gov or https://
www.fda.gov/regulatory-information/
search-fda-guidance-documents.
Persons unable to download an
electronic copy of ‘‘Clarification of
Radiation Control Regulations for
Manufacturers of Diagnostic X-Ray
Equipment’’ may send an email request
to CDRH-Guidance@fda.hhs.gov to
receive an electronic copy of the
document. Please use the document
number GUI01500029 and complete
title to identify the guidance you are
requesting.
III. Paperwork Reduction Act of 1995
While this guidance contains no new
collection of information, it does refer to
previously approved FDA collections of
information. The previously approved
collections of information are subject to
review by the Office of Management and
Budget (OMB) under the Paperwork
Reduction Act of 1995 (PRA) (44 U.S.C.
3501–3521). The collections of
information in the following FDA table
have been approved by OMB:
21 CFR Part or FDA Form
Topic
1002, 1005, 1010, 1020, 1030, 1040, and 1050; form FDA
2579 and form FDA 2877.
800, 801, and 809 ...................................................................
812 ...........................................................................................
‘‘Allegations of Regulatory Misconduct’’ form ..........................
Reporting and Recordkeeping for Electronic Products—General Requirements.
Labeling ...................................................................................
Investigational Device Exemption ...........................................
Voluntary Allegations of Regulatory Misconduct ....................
Dated: September 25, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
ACTION:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA–2024–N–0758, FDA–
2024–N–2032, FDA–2023–N–3847, and FDA–
2024–N–1201]
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approvals
Food and Drug Administration,
HHS.
The Food and Drug
Administration (FDA) is publishing a
list of information collections that have
been approved by the Office of
Management and Budget (OMB) under
the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT:
Amber Sanford, Office of Operations,
Food and Drug Administration, Three
White Flint North, 10A–12M, 11601
Landsdown St., North Bethesda, MD
20852, 301–796–8867, PRAStaff@
fda.hhs.gov.
SUMMARY:
[FR Doc. 2024–22332 Filed 9–27–24; 8:45 am]
AGENCY:
Notice.
OMB Control No.
0910–0025
0910–0485
0910–0078
0910–0769
The OMB control number and
expiration date of OMB approval for
each information collection are shown
in table 1. Copies of the supporting
statements for the information
collections are available on the internet
at https://www.reginfo.gov/public/do/
PRAMain. An Agency may not conduct
or sponsor, and a person is not required
to respond to, a collection of
information unless it displays a
currently valid OMB control number.
The
following is a list of FDA information
collections recently approved by OMB
under section 3507 of the Paperwork
Reduction Act of 1995 (44 U.S.C. 3507).
SUPPLEMENTARY INFORMATION:
TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB
Title of collection
OMB control No.
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New Plant Varieties Intended for Food Use ................................................................................................
Food and Cosmetic Export Certificates .......................................................................................................
Biological Products; General Records and Postmarket Adverse Experience Reporting ............................
Voluntary Total Product Life Cycle Advisory Program Pilot ........................................................................
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0910–0583
0910–0793
0910–0308
0910–0930
30SEN1
Date approval
expires
9/30/2027
9/30/2027
9/30/2027
9/30/2027
Federal Register / Vol. 89, No. 189 / Monday, September 30, 2024 / Notices
Dated: September 24, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–22291 Filed 9–27–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Recharter for the Council on Graduate
Medical Education
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
ACTION: Notice.
AGENCY:
In accordance with the
Federal Advisory Committee Act, the
Department of Health and Human
Services is hereby giving notice that the
Council on Graduate Medical Education
(COGME or Council) is rechartered.
DATES: The effective date of the renewed
charter is September 30, 2024.
FOR FURTHER INFORMATION CONTACT:
Shane Rogers, Designated Federal
Official (DFO), Division of Medicine
and Dentistry, Bureau of Health
Workforce, HRSA, 5600 Fishers Lane,
Room 15N142, Rockville, Maryland
20857; 301–443–5260; or srogers@
hrsa.gov.
SUPPLEMENTARY INFORMATION: COGME
makes recommendations to the
Secretary of Health and Human Services
and Congress on matters specified by
section 762 of the Public Health Service
Act. Issues addressed by COGME
include: (1) the supply and distribution
of physicians in the United States; (2)
current and future shortages or excesses
of physicians in medical and surgical
specialties and subspecialties; (3) issues
relating to internationalmedical school
graduates; (4) appropriate federal
policies with respect to the matters
specified in (1), (2), and (3) above,
including policies concerning changes
in the financing of undergraduate and
graduate medical education programs
and changes in the types of medical
education training in graduate medical
education programs; (5) appropriate
efforts to be carried out by hospitals,
schools of medicine, schools of
osteopathic medicine, and accrediting
bodies with respect to the matters
specified in (1), (2), and (3) above,
including efforts for changes in
undergraduate and graduate medical
education programs; and (6) deficiencies
in, and needs for improvements in,
existing databases concerning the
supply and distribution of, and
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postgraduate training programs for,
physicians in the United States and
steps that should be taken to eliminate
those deficiencies. Not later than
September 30, 2023, and not less than
every 5 years thereafter, COGME shall
submit a report on the recommendations
made by the committee to the Secretary
of Health and Human Services, and to
the Committee on Health, Education,
Labor, and Pensions of the Senate and
the Committee on Energy and
Commerce of the House of
Representatives. Additionally, COGME
encourages entities providing graduate
medical education to conduct activities
to voluntarily achieve the
recommendations of the Council;
develops, publishes, and implements
performance measures; develops and
publishes guidelines for longitudinal
evaluations; and recommends
appropriation levels for certain
programs under title VII of the Public
Health Service Act.
The renewed charter for COGME was
approved on September 18, 2024. The
filing date is September 30, 2024. The
recharter of COGME gives authorization
for the Council to operate until
September 30, 2026.
A copy of the COGME charter is
available on the COGME website at
https://www.hrsa.gov/sites/default/files/
hrsa/advisory-committees/graduatemedical-edu/cogme-charter.pdf. A copy
of the charter also can be obtained by
accessing the FACA database that is
maintained by the Committee
Management Secretariat under the
General Services Administration. The
website address for the FACA database
is https://www.facadatabase.gov/.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2024–22256 Filed 9–27–24; 8:45 am]
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Person listed below in advance of the
meeting. The meeting can be accessed
from the NIH Videocast at the following
link: https://videocast.nih.gov/.
Name of Committee: Office of AIDS
Research Advisory Council.
Date: October 24, 2024.
Time: 12:00 p.m. to 5:00 p.m.
Agenda: Report from the OAR Director;
Update on the Development of the NIH
Strategic Plan and Research Priorities for HIV
Research.
Place: Office of AIDS Research, Office of
the Director, NIH, 5601 Fishers Lane,
Rockville, MD 20852, (Virtual Meeting)
https://videocast.nih.gov/.
Contact Person: CAPT Mary Glenshaw,
Ph.D., M.P.H., OTR/L, Office of AIDS
Research, Office of the Director, NIH, 5601
Fishers Lane, Room 2E61, Rockville, MD
20852, (301) 496–0357, OARACinfo@nih.gov.
Any interested person may file written
comments with the committee 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:
www.oar.nih.gov, where an agenda and any
additional information for the meeting will
be posted when available.
(Catalogue of Federal Domestic Assistance
Program Nos. 93.14, Intramural Research
Training Award; 93.22, Clinical Research
Loan Repayment Program for Individuals
from Disadvantaged Backgrounds; 93.232,
Loan Repayment Program for Research
Generally; 93.39, Academic Research
Enhancement Award; 93.936, NIH Acquired
Immunodeficiency Syndrome Research Loan
Repayment Program; 93.187, Undergraduate
Scholarship Program for Individuals from
Disadvantaged Backgrounds, National
Institutes of Health, HHS)
Dated: September 24, 2024.
Lauren A. Fleck,
Program Analyst, Office of Federal Advisory
Committee Policy.
[FR Doc. 2024–22274 Filed 9–27–24; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Office of the Director, National
Institutes of Health; Notice of Meeting
Pursuant to section 1009 of the
Federal Advisory Committee Act, as
amended, notice is hereby given of a
meeting of the Office of AIDS Research
Advisory Council.
The meeting will be held as a virtual
meeting and will be open to the public
as indicated below. Individuals who
plan to view the virtual meeting and
need special assistance or other
reasonable accommodations to view the
meeting, should notify the Contact
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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
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[Federal Register Volume 89, Number 189 (Monday, September 30, 2024)]
[Notices]
[Pages 79626-79627]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-22291]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2024-N-0758, FDA-2024-N-2032, FDA-2023-N-3847, and
FDA-2024-N-1201]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Food and Drug Administration (FDA) is publishing a list of
information collections that have been approved by the Office of
Management and Budget (OMB) under the Paperwork Reduction Act of 1995.
FOR FURTHER INFORMATION CONTACT: Amber Sanford, Office of Operations,
Food and Drug Administration, Three White Flint North, 10A-12M, 11601
Landsdown St., North Bethesda, MD 20852, 301-796-8867,
[email protected].
SUPPLEMENTARY INFORMATION: The following is a list of FDA information
collections recently approved by OMB under section 3507 of the
Paperwork Reduction Act of 1995 (44 U.S.C. 3507). The OMB control
number and expiration date of OMB approval for each information
collection are shown in table 1. Copies of the supporting statements
for the information collections are available on the internet at
https://www.reginfo.gov/public/do/PRAMain. An Agency may not conduct or
sponsor, and a person is not required to respond to, a collection of
information unless it displays a currently valid OMB control number.
Table 1--List of Information Collections Approved by OMB
------------------------------------------------------------------------
Date approval
Title of collection OMB control No. expires
------------------------------------------------------------------------
New Plant Varieties Intended for 0910-0583 9/30/2027
Food Use.........................
Food and Cosmetic Export 0910-0793 9/30/2027
Certificates.....................
Biological Products; General 0910-0308 9/30/2027
Records and Postmarket Adverse
Experience Reporting.............
Voluntary Total Product Life Cycle 0910-0930 9/30/2027
Advisory Program Pilot...........
------------------------------------------------------------------------
[[Page 79627]]
Dated: September 24, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024-22291 Filed 9-27-24; 8:45 am]
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