Agency Information Collection Activities; Announcement of Office of Management and Budget Approvals, 8682 [2024-02579]
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Federal Register / Vol. 89, No. 27 / Thursday, February 8, 2024 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Notice of Closed Meeting
Pursuant to 5 U.S.C. 1009(d), notice is
hereby given of the following meeting.
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, and the Determination of
the Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, CDC, pursuant to Public Law
92–463. 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.
Name of Committee: Disease,
Disability, and Injury Prevention and
Control Special Emphasis Panel (SEP)—
DP24–031, Epidemiologic Cohort Study
of Interstitial Cystitis.
Date: April 10, 2024.
Time: 10 a.m.–6 p.m., EDT.
Place: Teleconference/Web
Conference.
Agenda: To review and evaluate grant
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For Further Information Contact:
Catherine Barrett, Ph.D., Scientific
Review Officer, National Center for
Chronic Disease Prevention and Health
Promotion, Centers for Disease Control
and Prevention, 4770 Buford Highway,
Mailstop S106–3, Atlanta, Georgia
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Business Initiatives, Office of the Chief
Operating Officer, Centers for Disease
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delegated the authority to sign Federal
Register notices pertaining to
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both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
[FR Doc. 2024–02514 Filed 2–7–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA–2023–N–2894; FDA–
2023–N–1929; FDA–2017–N–5569; FDA–
2023–N–2564; FDA–2023–N–2851; FDA–
2023–N–1554]
ACTION:
Notice.
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.
SUMMARY:
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.
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.
SUPPLEMENTARY INFORMATION:
Agency Information Collection
Activities; Announcement of Office of
Management and Budget Approvals
AGENCY:
Food and Drug Administration,
HHS.
TABLE 1—LIST OF INFORMATION COLLECTIONS APPROVED BY OMB
Title of collection
OMB control No.
Good Laboratory Practice (GLP) Regulations for Nonclinical Laboratory Studies .........................................
Orphan Drugs ..................................................................................................................................................
Medical Devices; Device Tracking ..................................................................................................................
Channels of Trade Policy for Commodities with Residues of Pesticide Chemicals for Which Tolerances
Have Been Revoked, Suspended, or Modified by the EPA ........................................................................
Time and Extent Applications for Nonprescription Drug Products ..................................................................
Qualitative Feedback on Food and Drug Administration Service Delivery .....................................................
Dated: February 5, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–02579 Filed 2–7–24; 8:45 am]
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Date approval
expires
0910–0119
0910–0167
0910–0442
1/31/2027
1/31/2027
1/31/2027
0910–0562
0910–0688
0910–0697
1/31/2027
1/31/2027
1/31/2027
]]>Agencies
[Federal Register Volume 89, Number 27 (Thursday, February 8, 2024)]
[Notices]
[Page 8682]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-02579]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2023-N-2894; FDA-2023-N-1929; FDA-2017-N-5569; FDA-
2023-N-2564; FDA-2023-N-2851; FDA-2023-N-1554]
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
------------------------------------------------------------------------
Good Laboratory Practice (GLP) 0910-0119 1/31/2027
Regulations for Nonclinical
Laboratory Studies.................
Orphan Drugs........................ 0910-0167 1/31/2027
Medical Devices; Device Tracking.... 0910-0442 1/31/2027
Channels of Trade Policy for 0910-0562 1/31/2027
Commodities with Residues of
Pesticide Chemicals for Which
Tolerances Have Been Revoked,
Suspended, or Modified by the EPA..
Time and Extent Applications for 0910-0688 1/31/2027
Nonprescription Drug Products......
Qualitative Feedback on Food and 0910-0697 1/31/2027
Drug Administration Service
Delivery...........................
------------------------------------------------------------------------
Dated: February 5, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024-02579 Filed 2-7-24; 8:45 am]
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