Notices. Notice
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/register/2023/12/22/2023-28290·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
BILLING CODE 4164-01-P 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. 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, *PRAStaff@fda.hhs.gov.* 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 Title of collection OMB control No. Date approval expires Generic Clearance for Qualitative Data to Support Social and Behavioral Research for Food, Dietary Supplements, Cosmetics, and Animal Food and Feed 0910-0891 9/30/2026 Medical Devices—Voluntary Improvement Program 0910-0922 9/30/2026 Submission of Petitions: Food Additive, Color Additive (Including Labeling), Submission of Information to a Master File in Support of Petitions, and Electronic Submission Using FDA Form 3503 0910-0016 10/31/2026 Infant Formula Requirements 0910-0256 10/31/2026 Biologics License Applications; Procedures & Requirements 0910-0338 10/31/2026 Medical Devices; Reports of Corrections and Removals 0910-0359 10/31/2026 Customer/Partner Satisfaction Service Surveys 0910-0360 10/31/2026 Voluntary National Retail Food Regulatory Program Standards 0910-0621 10/31/2026 Expanded Access to Investigational Drugs for Treatment Use 0910-0814 10/31/2026 Food Canning Establishment Registration, Process Filing and Recordkeeping for Acidified and Thermally Processed Low-Acid Foods 0910-0037 11/30/2026 Color Additive Certification 0910-0216 11/30/2026 Reporting and Recordkeeping Requirements for Reportable Food 0910-0643 11/30/2026 Prescription Drug Advertisements; Presentation of Advertisements in Television and Radio 0910-0686 11/30/2026 Submission to CDRH Allegations of Regulatory Misconduct Associated with Medical Devices 0910-0769 11/30/2026 Importation of Prescription Drugs 0910-0888 11/30/2026 Dated: December 19, 2023. Lauren K. Roth, Associate Commissioner for Policy. [FR Doc. 2023-28290 Filed 12-21-23; 8:45 am]
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