[Federal Register Volume 88, Number 245 (Friday, December 22, 2023)]
[Notices]
[Pages 88635-88636]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-28290]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Food and Drug Administration
[Docket Nos. FDA-2023-N-1157; FDA-2022-D-0109; FDA-2020-N-0908; FDA-
2022-D-0814; FDA-2022-D-0745; FDA-2023-N-1006; FDA-2023-N-1053; FDA-
2023-N-2286; FDA-2023-N-1661; FDA-2013-N-1119; FDA-2023-N-2986; FDA-
2009-N-0582; FDA-2023-N-1272; FDA-2023-N-2030; FDA-2023-N-1189]
Agency Information Collection Activities; Announcement of Office
of Management and Budget Approvals
AGENCY: Food and Drug Administration, HHS.
ACTION: Notice.
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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: 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,
[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).
[[Page 88636]]
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
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OMB control Date approval
Title of collection No. expires
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Generic Clearance for Qualitative Data 0910-0891 9/30/2026
to Support Social and Behavioral
Research for Food, Dietary Supplements,
Cosmetics, and Animal Food and Feed....
Medical Devices--Voluntary Improvement 0910-0922 9/30/2026
Program................................
Submission of Petitions: Food Additive, 0910-0016 10/31/2026
Color Additive (Including Labeling),
Submission of Information to a Master
File in Support of Petitions, and
Electronic Submission Using FDA Form
3503...................................
Infant Formula Requirements............. 0910-0256 10/31/2026
Biologics License Applications; 0910-0338 10/31/2026
Procedures & Requirements..............
Medical Devices; Reports of Corrections 0910-0359 10/31/2026
and Removals...........................
Customer/Partner Satisfaction Service 0910-0360 10/31/2026
Surveys................................
Voluntary National Retail Food 0910-0621 10/31/2026
Regulatory Program Standards...........
Expanded Access to Investigational Drugs 0910-0814 10/31/2026
for Treatment Use......................
Food Canning Establishment Registration, 0910-0037 11/30/2026
Process Filing and Recordkeeping for
Acidified and Thermally Processed Low-
Acid Foods.............................
Color Additive Certification............ 0910-0216 11/30/2026
Reporting and Recordkeeping Requirements 0910-0643 11/30/2026
for Reportable Food....................
Prescription Drug Advertisements; 0910-0686 11/30/2026
Presentation of Advertisements in
Television and Radio...................
Submission to CDRH Allegations of 0910-0769 11/30/2026
Regulatory Misconduct Associated with
Medical Devices........................
Importation of Prescription Drugs....... 0910-0888 11/30/2026
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Dated: December 19, 2023.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2023-28290 Filed 12-21-23; 8:45 am]
BILLING CODE 4164-01-P