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, 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 |
---|---|---|
Temporary Marketing Permit Applications | 0910–0133 | 1/31/2027 |
State Petitions for Exemption from Preemption | 0910–0277 | 1/31/2027 |
FDA Focus Groups and Interviews | 0910–0497 | 1/31/2027 |
Product Jurisdiction and Combination Products | 0910–0523 | 1/31/2027 |
Cosmetic Labeling and Cosmetic Registration | 0910–0599 | 1/31/2027 |
Registration of Human Drug Compounding Outsourcing Facilities under Section 503B of the FFDCA and Associated Fees under Section 744K | 0910–0776 | 1/31/2027 |
Dated: January 17, 2024.
Lauren K. Roth,
Associate Commissioner for Policy.
[FR Doc. 2024–01153 Filed 1–22–24; 8:45 am]
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